PMID-sentid Pub_year Sent_text comp_official_name comp_offset protein_name organism prot_offset 2773511-6 1989 The pathways of metabolism of ethacizin include N-de-ethylation, sulphoxidation, N-10 amide hydrolysis, aromatic hydroxylation and conjugation. diethylamino-ethmozine 30-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-85 2656675-8 1989 The remainder of the radioactivity from papain or Pronase digests of TR-1 eluted, like the TR-3 fractions, in the salt fraction on Sepharose CL-4B. Salts 114-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-95 2656675-8 1989 The remainder of the radioactivity from papain or Pronase digests of TR-1 eluted, like the TR-3 fractions, in the salt fraction on Sepharose CL-4B. Sepharose CL 4B 131-146 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-95 2656675-9 1989 Peptide mapping of the nonglycosylated TR-3 fraction by TLC and high voltage electrophoresis yielded six principal and several less intensely stained ninhydrin reactive components, with the radiolabel concentrated in one of the latter peptides. Ninhydrin 150-159 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-43 3271463-2 1987 Both are in the free base form and have an intramolecular-hydrogen bond between N10 of the acridine and the nitrogen atom of the carboxamide substituent. Hydrogen 58-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-83 3240918-3 1988 In the first group (N = 10), a single 20-mg dose of the slow-release formulation caused an increase in 8-h sodium excretion (P less than 0.025) and urine volume (P less than 0.005). Sodium 107-113 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-26 2626032-1 1989 Complementary DNAs (cDNAs) encoding a member of steroid receptor super-family, named TR3 receptor, were isolated from a human prostate lambda gt11 cDNA library on the basis of homology of oligonucleotide probes to the DNA-binding domain common to members of the steroid receptor super-family. Oligonucleotides 188-203 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-88 3271463-2 1987 Both are in the free base form and have an intramolecular-hydrogen bond between N10 of the acridine and the nitrogen atom of the carboxamide substituent. Acridines 91-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-83 3271463-2 1987 Both are in the free base form and have an intramolecular-hydrogen bond between N10 of the acridine and the nitrogen atom of the carboxamide substituent. Nitrogen 108-116 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-83 3271463-2 1987 Both are in the free base form and have an intramolecular-hydrogen bond between N10 of the acridine and the nitrogen atom of the carboxamide substituent. carboxamide 129-140 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-83 3561925-0 1987 Aromatisation of androstenedione by human breast cancer tissue: correlation with hormone receptor activity and possible biologic significance. Androstenedione 17-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 3652558-3 1987 Although the pathophysiology of this disorder remains to be demonstrated, a defect may be present, linking hormone-receptor cyclic AMP-mediated processes with abnormalities in parasympathetic and voluntary neuronal innervation or transmission. Cyclic AMP 124-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-123 3001307-1 1986 The relative binding affinities of 48 steroids for four classes of hormone receptor (progestin, PR; androgen, AR; glucocorticoid, GR; mineralocorticoid, MR) have been analyzed by correspondence analysis. Steroids 38-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-83 3792219-3 1986 The hormone receptor status was determined with the dextran-coated charcoal method. Dextrans 52-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-20 3789431-5 1986 Thiopental increased the latency of N10, N14, and N20. Thiopental 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 36-39 2431651-7 1986 Muscle ribonucleic acid content rose significantly in response to testosterone administration, suggesting that testosterone initiated its effect by hormone receptor interaction with muscle nuclei. Testosterone 66-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 148-164 2431651-7 1986 Muscle ribonucleic acid content rose significantly in response to testosterone administration, suggesting that testosterone initiated its effect by hormone receptor interaction with muscle nuclei. Testosterone 111-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 148-164 3018913-4 1986 Treatment with methimazol however increased the nuclear T4 binding, suggesting either a direct effect of methimazol on the hormone-receptor interaction or that the patients had become slightly hypothyroid during the treatment. Methimazole 15-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-139 3018913-4 1986 Treatment with methimazol however increased the nuclear T4 binding, suggesting either a direct effect of methimazol on the hormone-receptor interaction or that the patients had become slightly hypothyroid during the treatment. Methimazole 105-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-139 2423167-8 1985 Serosal La3+ apparently inactivates the hormone-receptor interaction and/or the link between the ADH-receptor complex and the activation of adenylate cyclase, but does not interfere with the operation of the Na+ "pump", the basal activity of adenylate cyclase or any of the intracellular events that mediate the effect of ADH on Na+ transport. lanthanum(3+) 8-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-56 2932536-3 1985 Magnesium is proposed to stabilize the hormone-receptor-guanine nucleotide regulatory protein complex, whereas sodium appears to destabilize this ternary complex. Magnesium 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-55 3971985-5 1985 The chromophoric N10 is efficiently solvent-protected, the solvent-dependence of its 15N resonance resulting from solvent interactions at other positions of the molecule and from solvent-dependent changes in the twisting of the chromophoric system. 15n 85-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-20 2999175-0 1986 Receptor-positive hereditary resistance to 1,25-dihydroxyvitamin D: chromatography of hormone-receptor complexes on deoxyribonucleic acid-cellulose shows two classes of mutation. 1,25-dihydroxyvitamin D 43-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-102 2999175-0 1986 Receptor-positive hereditary resistance to 1,25-dihydroxyvitamin D: chromatography of hormone-receptor complexes on deoxyribonucleic acid-cellulose shows two classes of mutation. deoxyribonucleic acid-cellulose 116-147 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-102 2999175-4 1986 With cells from two kindreds in whom there was mildly decreased localization of the hormone-receptor complex to the nucleus in vitro, occupied receptor interacted abnormally with DNA-cellulose (elution at 0.09-0.13 M KCl vs. normal at 0.20-0.26 M KCl); this suggested mutation(s) that affected a DNA-binding domain of the receptor in these two kindreds. Cellulose 183-192 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-100 2999175-4 1986 With cells from two kindreds in whom there was mildly decreased localization of the hormone-receptor complex to the nucleus in vitro, occupied receptor interacted abnormally with DNA-cellulose (elution at 0.09-0.13 M KCl vs. normal at 0.20-0.26 M KCl); this suggested mutation(s) that affected a DNA-binding domain of the receptor in these two kindreds. Potassium Chloride 217-220 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-100 2999175-4 1986 With cells from two kindreds in whom there was mildly decreased localization of the hormone-receptor complex to the nucleus in vitro, occupied receptor interacted abnormally with DNA-cellulose (elution at 0.09-0.13 M KCl vs. normal at 0.20-0.26 M KCl); this suggested mutation(s) that affected a DNA-binding domain of the receptor in these two kindreds. Potassium Chloride 247-250 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-100 2413033-7 1985 Formation of the disulfide-linked complexes requires 125I-FSH, specifically bound to the hormone receptor and cross-linking, and can be prevented with an excess of native FSH but not human choriogonadotropin. Disulfides 17-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-105 6848976-2 1983 Infants receiving the dorsal penile nerve block with lidocaine (1% Xylocaine) (N = 20) experienced significantly less stress, as evidenced by smaller decreases in transcutaneous oxygen pressure levels, less time spent crying, and smaller increases in heart rate, than infants circumcised in an identical manner without anesthetic (N = 10). Lidocaine 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 331-337 6721511-3 1984 At dichophase , prior to the onset of the S-stage in cell division cycle, under conjugation of progesterone with a certain specific type of protein (hormone receptor) the cells are induced toward the development of secretory function, i.e. toward differentiation, resulting in no synthesis of DNA. Progesterone 95-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-165 6500843-0 1984 Quantitative and qualitative effects of N10-methylfolate on high-affinity folate binding in human leukocytes. Folic Acid 50-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-43 6500843-1 1984 N10-methylfolate acted as a potent competitive inhibitor of high-affinity [3H] folate binding in human leukocytes, while methotrexate had no effect. [3h] folate 74-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-3 6500843-2 1984 Furthermore, folate binding changed into a non-cooperative type in the presence of N10-methylfolate. Folic Acid 13-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-86 6310288-8 1983 The results indicate that GDP is not released prior to but rather coincident with formation of the complex of the hormone receptor with the regulatory protein and that enzyme activation proceeds with the same time course as agonist binds to the receptor. Guanosine Diphosphate 26-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-130 6361354-1 1983 In this study involving 45 patients with the normal function of the sinus node and 10 patients showing signs of its damage (n-10), intravenous administration of ethmozine in a dose of 150 mg (1.5-2 mg/kg) exerted atropine like action. Moricizine 161-170 nuclear receptor subfamily 4 group A member 1 Homo sapiens 124-128 86543-0 1979 Reduction of GTP activation of adenylate cyclase system by its coupling to hormone receptor. Guanosine Triphosphate 13-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 6293818-9 1982 Based on the similarities between the data from these three systems and published data from other systems, we now propose that dithiol-disulfide interchange may play a general role in membrane-related processes such as transport, energy transduction and hormone-receptor interactions. dithiol 127-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 254-270 6293818-9 1982 Based on the similarities between the data from these three systems and published data from other systems, we now propose that dithiol-disulfide interchange may play a general role in membrane-related processes such as transport, energy transduction and hormone-receptor interactions. Disulfides 135-144 nuclear receptor subfamily 4 group A member 1 Homo sapiens 254-270 7451368-1 1980 Using 13C-NMR and mass spectral analysis we have demonstrated that the N-10 nitrogen of anthramycin is biosynthetically derived from the indole-nitrogen of tryptophan. 13c 6-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-75 7451368-1 1980 Using 13C-NMR and mass spectral analysis we have demonstrated that the N-10 nitrogen of anthramycin is biosynthetically derived from the indole-nitrogen of tryptophan. Anthramycin 88-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-75 7451368-1 1980 Using 13C-NMR and mass spectral analysis we have demonstrated that the N-10 nitrogen of anthramycin is biosynthetically derived from the indole-nitrogen of tryptophan. indole nitrogen 137-152 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-75 7451368-1 1980 Using 13C-NMR and mass spectral analysis we have demonstrated that the N-10 nitrogen of anthramycin is biosynthetically derived from the indole-nitrogen of tryptophan. Tryptophan 156-166 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-75 7451368-3 1980 From resonance intensities and 13C-15N spin-spin coupling in the 13C-NMR spectrum of didehydroanhydroanthramycin, a derivative of anthramycin, we could then determine the 13C enrichment at C-11 and the proportion of 13C bonded to 15N at N-10. 13c 65-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-241 7451368-3 1980 From resonance intensities and 13C-15N spin-spin coupling in the 13C-NMR spectrum of didehydroanhydroanthramycin, a derivative of anthramycin, we could then determine the 13C enrichment at C-11 and the proportion of 13C bonded to 15N at N-10. didehydroanhydroanthramycin 85-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-241 7451368-3 1980 From resonance intensities and 13C-15N spin-spin coupling in the 13C-NMR spectrum of didehydroanhydroanthramycin, a derivative of anthramycin, we could then determine the 13C enrichment at C-11 and the proportion of 13C bonded to 15N at N-10. Anthramycin 101-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-241 7451368-3 1980 From resonance intensities and 13C-15N spin-spin coupling in the 13C-NMR spectrum of didehydroanhydroanthramycin, a derivative of anthramycin, we could then determine the 13C enrichment at C-11 and the proportion of 13C bonded to 15N at N-10. 13c 65-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-241 7451368-3 1980 From resonance intensities and 13C-15N spin-spin coupling in the 13C-NMR spectrum of didehydroanhydroanthramycin, a derivative of anthramycin, we could then determine the 13C enrichment at C-11 and the proportion of 13C bonded to 15N at N-10. 13c 65-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-241 7451368-4 1980 These results when combined with mass spectral analysis and isotopic dilution measurements proved that the indole nitrogen of tryptophan was completely retained at N-10 of anthramycin. indole 107-113 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-168 7451368-4 1980 These results when combined with mass spectral analysis and isotopic dilution measurements proved that the indole nitrogen of tryptophan was completely retained at N-10 of anthramycin. Nitrogen 114-122 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-168 7451368-4 1980 These results when combined with mass spectral analysis and isotopic dilution measurements proved that the indole nitrogen of tryptophan was completely retained at N-10 of anthramycin. Tryptophan 126-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-168 7451368-4 1980 These results when combined with mass spectral analysis and isotopic dilution measurements proved that the indole nitrogen of tryptophan was completely retained at N-10 of anthramycin. Anthramycin 172-183 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-168 222810-6 1979 The relase of the BK-A is calcium and temperature dependent, requires metabolic energy, and is controlled by hormone-receptor interactions that influence the cellular level of cyclic AMP, as has been described for other mediators of immediate hypersensitivity reactions. Calcium 26-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-125 222810-6 1979 The relase of the BK-A is calcium and temperature dependent, requires metabolic energy, and is controlled by hormone-receptor interactions that influence the cellular level of cyclic AMP, as has been described for other mediators of immediate hypersensitivity reactions. Cyclic AMP 176-186 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-125 6243863-6 1980 These results suggest that in intact luteal cells danazol inhibits steroidogenesis at a point distal to hormone-receptor interaction and cAMP formation. Danazol 50-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 86543-9 1979 Furthermore, in plasma membranes isolated from butyrate-treated cells, the hormone receptor is sensitive to GTP; i.e. GTP reduces the affinity of isoproterenol for the receptor. Butyrates 47-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 86543-9 1979 Furthermore, in plasma membranes isolated from butyrate-treated cells, the hormone receptor is sensitive to GTP; i.e. GTP reduces the affinity of isoproterenol for the receptor. Guanosine Triphosphate 108-111 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 86543-9 1979 Furthermore, in plasma membranes isolated from butyrate-treated cells, the hormone receptor is sensitive to GTP; i.e. GTP reduces the affinity of isoproterenol for the receptor. Guanosine Triphosphate 118-121 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 86543-9 1979 Furthermore, in plasma membranes isolated from butyrate-treated cells, the hormone receptor is sensitive to GTP; i.e. GTP reduces the affinity of isoproterenol for the receptor. Isoproterenol 146-159 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 220946-0 1978 Hormone receptor levels and metabolic activity in the uterus of the ewe: regulation by oestradiol and progesterone. Estradiol 87-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 717283-1 1978 Use of a liquid nitrogen container for convenient transport of frozen mammary carcinoma tissue for hormone-receptor assays is described. Nitrogen 16-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-115 675244-2 1978 The highest quantum yield of solvated electrons (about 0.03) was obtained for flavins containing tyrosine on a side chain in the isoalloxazine N-3 or N-10 position. Flavins 78-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-154 675244-2 1978 The highest quantum yield of solvated electrons (about 0.03) was obtained for flavins containing tyrosine on a side chain in the isoalloxazine N-3 or N-10 position. Tyrosine 97-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-154 510217-4 1979 The hydrogen bond directionality observed in T4 and other thyroid structures offers an insight into the molecular details of the hormone-receptor site. Hydrogen 4-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 129-145 220946-0 1978 Hormone receptor levels and metabolic activity in the uterus of the ewe: regulation by oestradiol and progesterone. Progesterone 102-114 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 720288-1 1978 A reliable procedure is described for isolating 3H-triamcinolone acetonide (3H-TA) receptor complexes from purified chronic lymphatic leukemia (CLL) lymphocyte nuclei, based on the use of carbobenzoxy-L-phenylalanine (CBZ-L-phe) to prevent breakdown of hormone-receptor complexes during extraction of nuclei with 0.6M KCl. Tritium 48-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 253-269 206276-5 1978 The inhibition is dependent on the photogeneration of the aryl nitrene intermediate and is relieved by protecting the hormone receptor with excess oxytocin (10(-6)M) during the photolysis. aryl nitrene 58-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-134 199464-0 1977 Hormone--receptor interactions: [4-carboranylalanine, 5-leucine]-enkephalin as a structural probe for the opiate receptor. [4-carboranylalanine 32-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-17 196828-0 1977 Control of hormone receptor levels and growth of 7,12-dimethylbenz(a)anthracene-induced mammary tumors by estrogens, progesterone and prolactin. anthracene 69-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-27 196828-0 1977 Control of hormone receptor levels and growth of 7,12-dimethylbenz(a)anthracene-induced mammary tumors by estrogens, progesterone and prolactin. Progesterone 117-129 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-27 190053-9 1976 Thus in PHP Type I, the lack of c-AMP response to PTH, coupled with the ability of infused DBc-AMP to evoke a normal renal response suggests that the metabolic defect in this disorder may exist in hormone receptor-adenyl cyclase complex. Bucladesine 91-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 197-213 190192-0 1976 [Synthesis of [D-alanine, 4"-azido-3",5"-ditritio-L-phenylalanine, norvaline4[alpha-melanotropin as a "photoaffinity probe" for hormone-receptor interactions (author"s transl)]. dalbergioidin 15-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 128-144 190192-0 1976 [Synthesis of [D-alanine, 4"-azido-3",5"-ditritio-L-phenylalanine, norvaline4[alpha-melanotropin as a "photoaffinity probe" for hormone-receptor interactions (author"s transl)]. 4"-azido-3",5"-ditritio-l-phenylalanine 26-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 128-144 190192-0 1976 [Synthesis of [D-alanine, 4"-azido-3",5"-ditritio-L-phenylalanine, norvaline4[alpha-melanotropin as a "photoaffinity probe" for hormone-receptor interactions (author"s transl)]. norvaline4 67-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 128-144 869360-3 1977 The development of hormone receptor analysis permits us to better understand the mechanisms of action of steroid and peptide hormones and increases the likelihood of using there hormonal agents effectively. Steroids 105-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-35 170999-3 1975 However, hormone-receptor interaction in the human cell does not lead to an increase in intracellular cyclic AMP concentration, but in the rat cell, hormone-receptor interaction does lead to a significant increase in cyclic AMP content. Cyclic AMP 217-227 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-165 1812-6 1975 The role of lipid mobility in modulating hormone-receptor interaction is discussed with reference to the binding of thyroid stimulating hormone. Thyrotropin 116-143 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-57 34051231-7 2021 Acan1 and Nak1 displayed anticolitic properties via significantly reducing weight loss and colon atrophy, oedema, ulceration, and necrosis in 2,4,6-trinitrobenzene sulfonic acid exposed mice. Trinitrobenzenesulfonic Acid 142-177 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-14 14042998-5 1963 On the basis of the results it was postulated that hormone-receptor interaction can be considered a two-step process: (a) The binding or attachment of hormone to receptor site through ionic, hydrogen, and hydrophobic bonds and (b) a disulfide interchange reaction between hormonal disulfide and receptor sulfhydryl. Hydrogen 191-199 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 14042998-5 1963 On the basis of the results it was postulated that hormone-receptor interaction can be considered a two-step process: (a) The binding or attachment of hormone to receptor site through ionic, hydrogen, and hydrophobic bonds and (b) a disulfide interchange reaction between hormonal disulfide and receptor sulfhydryl. Disulfides 233-242 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 14042998-5 1963 On the basis of the results it was postulated that hormone-receptor interaction can be considered a two-step process: (a) The binding or attachment of hormone to receptor site through ionic, hydrogen, and hydrophobic bonds and (b) a disulfide interchange reaction between hormonal disulfide and receptor sulfhydryl. Disulfides 281-290 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 14042998-5 1963 On the basis of the results it was postulated that hormone-receptor interaction can be considered a two-step process: (a) The binding or attachment of hormone to receptor site through ionic, hydrogen, and hydrophobic bonds and (b) a disulfide interchange reaction between hormonal disulfide and receptor sulfhydryl. Sulfhydryl Compounds 304-314 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 33684224-4 2021 RESULTS: Subtype shift (SS) of pBT in syLNs was observed in 28% cases for HR(+), in 6% cases for the HER2(+), and in 16% cases for the TN. (E)-2-(pent-3-en-1-yn-1-yl)thiophene 31-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-76 34037241-15 2021 This was largely accounted for by a moderate improvement in PFS for inclusion of capecitabine in hormone receptor-positive cancers (HR 0.82, 95% CI 0.73 to 0.91; 7 studies, 1594 participants; moderate-certainty evidence) compared to no difference in PFS for hormone receptor-negative cancers (HR 0.96, 95% CI 0.83 to 1.10; 7 studies, 1122 participants; moderate-certainty evidence). Capecitabine 81-93 nuclear receptor subfamily 4 group A member 1 Homo sapiens 258-274 34037241-27 2021 AUTHORS" CONCLUSIONS: In summary, a moderate PFS benefit by including capecitabine was seen only in hormone receptor-positive cancers in metastatic studies. Capecitabine 70-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 100-116 172127-2 1975 It is demonstrated that because of limitations in the magnitude of the specific activity of radiolabeled hormone derivatives, direct binding studies of hormone-receptor interactions of high affinity (10(-9) -10(-11) M, depending on whether 3H- or 123I-labeled hormones are used) will be subject to artifactual distortions due to the need to utilize high concentrations of the receptor. Tritium 240-242 nuclear receptor subfamily 4 group A member 1 Homo sapiens 152-168 172127-2 1975 It is demonstrated that because of limitations in the magnitude of the specific activity of radiolabeled hormone derivatives, direct binding studies of hormone-receptor interactions of high affinity (10(-9) -10(-11) M, depending on whether 3H- or 123I-labeled hormones are used) will be subject to artifactual distortions due to the need to utilize high concentrations of the receptor. Iodine-123 247-251 nuclear receptor subfamily 4 group A member 1 Homo sapiens 152-168 14404999-0 1960 The enzymatic conversion of N5-formyl tetrahydrofolic acid (folinic acid) to N10-formyl tetrahydrofolic acid. Leucovorin 28-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-80 14404999-0 1960 The enzymatic conversion of N5-formyl tetrahydrofolic acid (folinic acid) to N10-formyl tetrahydrofolic acid. Leucovorin 60-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-80 13250013-0 1955 On the occurrence of N10-formyltetrahydrofolic acid by enzymic formylation of tetrahydrofolic acid and on the mechanism of this reaction. 5,6,7,8-tetrahydrofolic acid 31-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 21-24 33617125-1 2021 Multicolor chemiluminescent acridinium derivatives were synthesized by attaching various common fluorophores to the N10 -acridinium position through a piperazine linker. acridinium I 28-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 116-119 33617125-1 2021 Multicolor chemiluminescent acridinium derivatives were synthesized by attaching various common fluorophores to the N10 -acridinium position through a piperazine linker. acridinium I 121-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 116-119 33617125-1 2021 Multicolor chemiluminescent acridinium derivatives were synthesized by attaching various common fluorophores to the N10 -acridinium position through a piperazine linker. piperazine 151-161 nuclear receptor subfamily 4 group A member 1 Homo sapiens 116-119 34037241-1 2021 BACKGROUND: Retrospective analyses suggest that capecitabine may carry superior activity in hormone receptor-positive relative to hormone receptor-negative metastatic breast cancer. Capecitabine 48-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-108 34037241-12 2021 In the metastatic setting, the effect of capecitabine was heterogenous between hormone receptor-positive and -negative tumours. Capecitabine 41-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-95 34037241-15 2021 This was largely accounted for by a moderate improvement in PFS for inclusion of capecitabine in hormone receptor-positive cancers (HR 0.82, 95% CI 0.73 to 0.91; 7 studies, 1594 participants; moderate-certainty evidence) compared to no difference in PFS for hormone receptor-negative cancers (HR 0.96, 95% CI 0.83 to 1.10; 7 studies, 1122 participants; moderate-certainty evidence). Capecitabine 81-93 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-113 34043967-0 2021 Malayoside, a Cardenolide Glycoside Extracted from Antiaris Toxicaria Lesch, Induces Apoptosis in Human Non-small Lung Cancer Cells via MAPK-Nur77 Signaling Pathway. Malayoside 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 141-146 34043967-8 2021 Meanwhile, malayoside induced Nur77 expression and mitochondrial localization, and its induction of apoptosis was Nur77-dependent. Malayoside 11-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-35 34043967-8 2021 Meanwhile, malayoside induced Nur77 expression and mitochondrial localization, and its induction of apoptosis was Nur77-dependent. Malayoside 11-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-119 34043967-9 2021 To investigate the molecular mechanism of malayoside inducing Nur77 and apoptosis, we found that malayoside activated MAPK signaling pathway, including both ERK and p38 phosphorylation. Malayoside 42-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 34043967-9 2021 To investigate the molecular mechanism of malayoside inducing Nur77 and apoptosis, we found that malayoside activated MAPK signaling pathway, including both ERK and p38 phosphorylation. Malayoside 97-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 34043967-10 2021 The suppression of MAPK signaling activation inhibited the expression of Nur77 and apoptosis induced by malayoside. Malayoside 104-114 nuclear receptor subfamily 4 group A member 1 Homo sapiens 73-78 34043967-13 2021 Our results suggest that malayoside possesses an anti-NSCLC activity in vitro and in vivo mainly via activation of MAPK-Nur77 signaling pathway, indicating that malayoside is a promising chemotherapeutic candidate for NSCLC. Malayoside 25-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-125 34043967-13 2021 Our results suggest that malayoside possesses an anti-NSCLC activity in vitro and in vivo mainly via activation of MAPK-Nur77 signaling pathway, indicating that malayoside is a promising chemotherapeutic candidate for NSCLC. Malayoside 161-171 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-125 34046009-7 2021 This stimulation regimen helped in providing optimum levels of r-hLH supplementation to patients with impaired hormone-receptor interacting activity, to achieve higher success in pregnancy and live birth rates. r-hlh 63-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-127 34037241-29 2021 In contrast, the addition of capecitabine in the adjuvant setting led to improved outcomes for OS and DFS in hormone receptor-negative cancer. Capecitabine 29-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-125 34014949-7 2021 However, N addition increased BG activity in the N5 and N10 additions in the sandy grassland, and in the N5, N10, and N15 additions in the semi-fixed sandy land. Nitrogen 9-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 56-59 34014949-7 2021 However, N addition increased BG activity in the N5 and N10 additions in the sandy grassland, and in the N5, N10, and N15 additions in the semi-fixed sandy land. Nitrogen 9-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-112 33990575-7 2021 Thus, TGFbeta converts Nur77"s role from destabilizing ID1 protein and cancer inhibition to inducing ID1 mRNA expression and cancer promotion, which is highly relevant to colon cancer stemness, metastasis and oxaliplatin resistance. Oxaliplatin 209-220 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-28 33909934-1 2021 BACKGROUND: The BYLieve trial (NCT03056755) confirmed efficacy and safety of alpelisib with fulvestrant for hormone receptor-positive (HR+), human epidermal growth factor receptor-2-negative (HER2-), PIK3CA-mutated advanced breast cancer (ABC), after cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) with an aromatase inhibitor (AI) as immediate prior therapy. Alpelisib 77-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-124 34006717-0 2021 [A Case of Hormone Receptor-Positive HER2-Negative Advanced/Recurrent Breast Cancer with 1.5 Years Withdrawal Period of Palbociclib Showed a Good Response Treated by Abemaciclib and Fulvestrant]. palbociclib 120-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-27 33968263-2 2021 Early results of the MonarchE trial investigating the addition of the cyclin-dependent kinase (CDK) 4/6 inhibitor abemaciclib to standard adjuvant endocrine therapy indicated a lower recurrence rate in the combination group in a high-risk population of patients with early stage hormone receptor (HR)-positive/HER2-negative BC. abemaciclib 114-125 nuclear receptor subfamily 4 group A member 1 Homo sapiens 279-295 33968263-2 2021 Early results of the MonarchE trial investigating the addition of the cyclin-dependent kinase (CDK) 4/6 inhibitor abemaciclib to standard adjuvant endocrine therapy indicated a lower recurrence rate in the combination group in a high-risk population of patients with early stage hormone receptor (HR)-positive/HER2-negative BC. abemaciclib 114-125 nuclear receptor subfamily 4 group A member 1 Homo sapiens 297-299 33657579-8 2021 Potassium stimulation caused DNA demethylation around cyclic AMP responsive element binding protein 1 (CREB1) and nuclear receptor subfamily 4 group A (NR4A) family-binding sites and a TSS; demethylation was accompanied by recruitment of CREB1 and NR4A1 and increased chromatin accessibility of the CYP11B2 promoter. Potassium 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 248-253 33910628-0 2021 Dual treatment of acromegaly and hormone-receptor-positive breast cancer with tamoxifen: a case report. Tamoxifen 78-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-49 33910628-3 2021 We describe the case of a patient who was treated successfully with tamoxifen for her hormone-receptor-positive breast cancer and acromegaly. Tamoxifen 68-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-102 33910628-8 2021 CONCLUSION: This case highlights the dual benefit of tamoxifen therapy in the treatment of hormone-receptor-positive breast cancer and acromegaly. Tamoxifen 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-107 33910628-9 2021 Unlike anastrozole, tamoxifen has the benefit of lowering insulin-like growth factor 1 levels, which underscores its advantage in reducing adverse musculoskeletal symptoms during the treatment of hormone-receptor-positive breast cancer. Tamoxifen 20-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 196-212 33910628-10 2021 We offer the first reported use of tamoxifen monotherapy for the successful treatment of acromegaly and hormone-receptor-positive breast cancer. Tamoxifen 35-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 33996592-0 2021 Effectiveness of a 6-Month 22.5-mg Leuprolide Acetate Depot Formulation With Tamoxifen for Postoperative Premenopausal Estrogen Suppression in Hormone Receptor-Positive Breast Cancer. Tamoxifen 77-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 143-159 33863896-1 2021 Expression of hormone receptor (HR) for estrogens (ER) and progesterone (PR) and HER2 remains the cornerstone to define the therapeutic strategy for breast cancer patients. Progesterone 59-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-30 33905134-0 2021 Final results of the randomized phase 2 LEO trial and bone protective effects of everolimus for premenopausal hormone receptor-positive, HER2-negative metastatic breast cancer. Everolimus 81-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-126 33905134-1 2021 The phase 2 LEO study showed that everolimus (EVE) plus letrozole (LET) with ovarian suppression increased progression-free survival (PFS) in tamoxifen-exposed premenopausal women with hormone receptor-positive, HER2-negative metastatic breast cancer with visceral metastases. Everolimus 34-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 185-201 33905134-1 2021 The phase 2 LEO study showed that everolimus (EVE) plus letrozole (LET) with ovarian suppression increased progression-free survival (PFS) in tamoxifen-exposed premenopausal women with hormone receptor-positive, HER2-negative metastatic breast cancer with visceral metastases. Letrozole 56-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 185-201 33905134-1 2021 The phase 2 LEO study showed that everolimus (EVE) plus letrozole (LET) with ovarian suppression increased progression-free survival (PFS) in tamoxifen-exposed premenopausal women with hormone receptor-positive, HER2-negative metastatic breast cancer with visceral metastases. Tamoxifen 142-151 nuclear receptor subfamily 4 group A member 1 Homo sapiens 185-201 33902205-4 2021 After the first cyclin-dependent kinase (CDK) 4/6 inhibitor Palbociclib entered the clinical application for HR positive and HER-2 negative advanced breast cancer patients in 2015, the clinical treatment pattern of HR positive and HER-2 negative advanced breast cancer has been changed significantly, with a consequent breakthrough improvement in patients" survival prognosis. palbociclib 60-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-111 33902205-4 2021 After the first cyclin-dependent kinase (CDK) 4/6 inhibitor Palbociclib entered the clinical application for HR positive and HER-2 negative advanced breast cancer patients in 2015, the clinical treatment pattern of HR positive and HER-2 negative advanced breast cancer has been changed significantly, with a consequent breakthrough improvement in patients" survival prognosis. palbociclib 60-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 215-217 33923503-0 2021 Broussochalcone A Is a Novel Inhibitor of the Orphan Nuclear Receptor NR4A1 and Induces Apoptosis in Pancreatic Cancer Cells. broussochalcone A 0-17 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-75 33923503-2 2021 In this study, we identified broussochalcone A (BCA) as a new NR4A1 inhibitor and demonstrated that BCA inhibits cell growth partly by inducing NR4A1-mediated apoptotic pathways in human pancreatic cancer cells. broussochalcone A 29-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 33923503-2 2021 In this study, we identified broussochalcone A (BCA) as a new NR4A1 inhibitor and demonstrated that BCA inhibits cell growth partly by inducing NR4A1-mediated apoptotic pathways in human pancreatic cancer cells. broussochalcone A 29-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-149 33923503-2 2021 In this study, we identified broussochalcone A (BCA) as a new NR4A1 inhibitor and demonstrated that BCA inhibits cell growth partly by inducing NR4A1-mediated apoptotic pathways in human pancreatic cancer cells. broussochalcone A 48-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 33863896-1 2021 Expression of hormone receptor (HR) for estrogens (ER) and progesterone (PR) and HER2 remains the cornerstone to define the therapeutic strategy for breast cancer patients. Progesterone 59-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-34 33258078-1 2021 PURPOSE: There are conflicting results on the potential role of HER2-status on the efficacy of aromatase inhibitors (AIs) and tamoxifen (TAM) in patients with hormone receptor (HR)-positive breast cancer (BC). Tamoxifen 126-135 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-175 33924348-3 2021 We designed a cyclodextrin (CD)-based polymeric complex to deliver chemotherapeutic doxorubicin (DOX) and Nur77DeltaDBD gene for combating pumps and non-pump resistance simultaneously. Cyclodextrins 14-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-119 33924348-3 2021 We designed a cyclodextrin (CD)-based polymeric complex to deliver chemotherapeutic doxorubicin (DOX) and Nur77DeltaDBD gene for combating pumps and non-pump resistance simultaneously. Cyclodextrins 28-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-119 33924348-7 2021 The polymeric inclusion complex can efficiently deliver the Nur77DeltaDBD gene than polyethylenimine (PEI-25k), which is a golden standard for nonviral vector gene delivery. Polyethyleneimine 84-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-73 33924348-7 2021 The polymeric inclusion complex can efficiently deliver the Nur77DeltaDBD gene than polyethylenimine (PEI-25k), which is a golden standard for nonviral vector gene delivery. pei 102-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-73 33868464-0 2021 Olaparib in hormone receptor-positive, HER2-negative metastatic breast cancer with a somatic BRCA2 mutation. olaparib 0-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-28 33987405-1 2021 Background: Palbociclib combined with endocrine therapy has been approved as a front-line treatment for hormone receptor positive (HR+), human epidermal growth factor receptor 2 negative (HER2-) advanced breast cancer (ABC). palbociclib 12-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 33258078-1 2021 PURPOSE: There are conflicting results on the potential role of HER2-status on the efficacy of aromatase inhibitors (AIs) and tamoxifen (TAM) in patients with hormone receptor (HR)-positive breast cancer (BC). Tamoxifen 137-140 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-175 33168657-1 2021 On May 24, 2019, the FDA granted regular approval to alpelisib in combination with fulvestrant for postmenopausal women, and men, with hormone receptor (HR)-positive, HER2-negative, phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA)-mutated, advanced or metastatic breast cancer as detected by an FDA-approved test following progression on or after an endocrine-based regimen. Alpelisib 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 135-157 33138346-3 2021 We analyzed the real-world clinical practice patterns and outcome in HR-positive, MBC Asian patients treated with palbociclib. palbociclib 114-125 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-71 33622114-0 2021 Alpelisib for the treatment of PIK3CA-mutated, hormone receptor-positive, HER2-negative metastatic breast cancer. Alpelisib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-63 33622114-3 2021 Alpelisib is a PI3K-alpha inhibitor and is the first PI3K inhibitor approved, in association with fulvestrant, by the FDA and EMA, based on improved progression-free survival (PFS) versus fulvestrant alone in a randomized phase III trial in HR+/HER2-, PIK3CA-mutated tumors following progression on/after HT.Areas covered: The scientific rationale, preclinical development, pharmacokinetics, and clinical efficacy/safety of alpelisib-fulvestrant are summarized. Alpelisib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 241-243 33622114-4 2021 The role of alpelisib in the clinical setting is discussed, referencing current therapeutic options and clinical challenges associated with alpelisib"s safety profile.Expert opinion: Alpelisib is an option for patients with HR+/HER2-, PIK3CA-mutated tumors whose disease progressed during/after aromatase inhibitor treatment. Alpelisib 183-192 nuclear receptor subfamily 4 group A member 1 Homo sapiens 224-226 33868173-1 2021 Background: Everolimus, an immunosuppressant, is approved for the treatment of advanced renal cell carcinoma, metastatic hormone receptor-positive breast cancer, and pancreatic neuroendocrine tumors (P-NETs) but has been reported to be related to hepatitis B reactivation. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-137 33683521-1 2021 PURPOSE: Treatment with Palbociclib, a cyclin-dependent kinase 4/6 inhibitor, has demonstrated significantly improved progression-free survival in patients with hormone receptor-positive, HER2-negative, advanced breast cancer, when used in combination with letrozole or fulvestrant endocrine therapies. palbociclib 24-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 161-177 33790765-0 2021 A Substantial Response from Adding Palbociclib to Endocrine Therapy in Brain Metastasis from Hormone Receptor-Positive, HER2-Negative Breast Cancer: Case Reports. palbociclib 35-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-109 33663585-0 2021 First in class dual MDM2/MDMX inhibitor ALRN-6924 enhances antitumor efficacy of chemotherapy in TP53 wild-type hormone receptor-positive breast cancer models. alrn-6924 40-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-128 33663585-12 2021 CONCLUSION: The significant synergy observed with ALRN-6924 in combination with chemotherapeutic agents supports further evaluation in patients with hormone receptor-positive breast cancer. alrn-6924 50-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-165 33757987-0 2021 Pre-existing effector T-cell levels and augmented myeloid cell composition denote response to CDK4/6 inhibitor palbociclib and pembrolizumab in hormone receptor-positive metastatic breast cancer. palbociclib 111-122 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-160 33737962-0 2021 High-dose tamoxifen in high-hormone-receptor-expressing advanced breast cancer patients: a phase II pilot study. Tamoxifen 10-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-44 33645243-0 2021 Cost-effectiveness of ribociclib plus endocrine therapy versus placebo plus endocrine therapy in HR-positive, HER2-negative breast cancer. ribociclib 22-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-99 33645243-1 2021 BACKGROUND: The 2015 American Society of Clinical Oncology guidelines recommend first-line treatment of hormone receptor (HR)-positive breast cancer with endocrine therapy plus or minus palbociclib, a selective cyclin-dependent kinase (CDK)4/6 inhibitor. palbociclib 186-197 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 33645243-1 2021 BACKGROUND: The 2015 American Society of Clinical Oncology guidelines recommend first-line treatment of hormone receptor (HR)-positive breast cancer with endocrine therapy plus or minus palbociclib, a selective cyclin-dependent kinase (CDK)4/6 inhibitor. palbociclib 186-197 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-124 33737962-3 2021 This study aimed to explore the efficacy of high-dose tamoxifen (TAM) treatment in patients with advanced breast cancer with highly expressed HR. Tamoxifen 54-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 142-144 33737962-3 2021 This study aimed to explore the efficacy of high-dose tamoxifen (TAM) treatment in patients with advanced breast cancer with highly expressed HR. Tamoxifen 65-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 142-144 33737962-14 2021 Conclusion: A high-dose of TAM is effective and safe for patients with advanced breast cancer with high HR expression. Tamoxifen 27-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-106 33596096-1 2021 BACKGROUND: Tamoxifen and aromatase inhibitors (AIs) are used as adjuvant hormonal therapy (AHT) for early-stage hormone receptor-positive (HR+) breast cancer. Tamoxifen 12-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-129 33527970-2 2021 Compounds Tr3, Tr7, Tr12, Tr15, and Tr16 exhibited good effect in inhibiting alpha-syn fibrillogenesis confirmed by Thioflavin-T assay and fluorescence microscopy and alpha-syn disaggregation confirmed by fluorescence microscopy. thioflavin T 116-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-13 33527970-4 2021 Compounds Tr3, Tr7, Tr12, Tr15 and Tr16 showed good binding interactions with the essential amino acid residues of alpha-syn. Amino Acids, Essential 82-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-13 33624592-0 2021 [Fuxinfang improves hypoxia-induced injury of human aortic endothelial cells by regulating c-Fos-NR4A1-p38 pathway]. fuxinfang 1-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-102 33460574-1 2021 BACKGROUND: Palbociclib added to endocrine therapy improves progression-free survival in hormone-receptor-positive, HER2-negative, metastatic breast cancer. palbociclib 12-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-105 33279290-3 2021 Previously we reported that BI1071(DIM-C-pPhCF3+MeSO3-), an oxidized form and methanesulfonate salt of (4-CF3-Ph-C-DIM), can modulate Nur77"s non-genomic apoptotic pathway through that Nur77 translocated from the nucleus to mitochondria to induce cytochrome c releasing and promote apoptosis of cancer cell. bi1071 28-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 134-139 33279290-3 2021 Previously we reported that BI1071(DIM-C-pPhCF3+MeSO3-), an oxidized form and methanesulfonate salt of (4-CF3-Ph-C-DIM), can modulate Nur77"s non-genomic apoptotic pathway through that Nur77 translocated from the nucleus to mitochondria to induce cytochrome c releasing and promote apoptosis of cancer cell. bi1071 28-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 185-190 33279290-3 2021 Previously we reported that BI1071(DIM-C-pPhCF3+MeSO3-), an oxidized form and methanesulfonate salt of (4-CF3-Ph-C-DIM), can modulate Nur77"s non-genomic apoptotic pathway through that Nur77 translocated from the nucleus to mitochondria to induce cytochrome c releasing and promote apoptosis of cancer cell. methanesulfonate salt 78-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 134-139 33547330-1 2021 The PvuII (rs2234693) Single Nucleotide Polymorphism (SNP) in the gene coding for the estrogen receptor-1 (ESR1), has been found associated with outcome in tamoxifen treated patients with early hormone-receptor positive breast cancer. Tamoxifen 156-165 nuclear receptor subfamily 4 group A member 1 Homo sapiens 194-210 33676870-0 2021 First-line Treatment with Ribociclib plus Endocrine Therapy for Premenopausal Women with Hormone-receptor-positive Advanced Breast Cancer: A Cost-effectiveness Analysis. ribociclib 26-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-105 33189785-6 2021 Substitution of two putative phylogenetically well-conserved small ubiquitin-like modifier (SUMO) acceptor sites, lysine 102 (K102) and 577 (K577) by arginine residues (R) modulated Nur77 transcriptional activity. Arginine 150-158 nuclear receptor subfamily 4 group A member 1 Homo sapiens 182-187 33198527-1 2021 INTRODUCTION: Patients with hormone receptor-positive/HER2-negative (HR+/HER2-) metastatic breast cancer have benefitted from treatment with palbociclib, a cyclin-dependent kinase (CDK) 4/6 inhibitor capable of selectively targeting mechanisms of cell cycle progression that contribute to tumor cell proliferation. palbociclib 141-152 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-44 33634624-0 2021 Palbociclib Plus Fulvestrant in Korean Patients from PALOMA-3 With Hormone Receptor-Positive/Human Epidermal Growth Factor Receptor 2-Negative Advanced Breast Cancer. palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-83 33634624-1 2021 In the PALOMA-3 trial, the median progression-free survival (PFS) was longer among patients with hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) advanced breast cancer (ABC) treated with palbociclib plus fulvestrant than those treated with placebo plus fulvestrant. palbociclib 229-240 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-113 33659039-0 2021 Phase 1 study of Z-endoxifen in patients with advanced gynecologic, desmoid, and hormone receptor-positive solid tumors. 4-hydroxy-N-desmethyltamoxifen 17-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 33540405-2 2021 Palbociclib combined with endocrine therapy has shown promising results in hormone-receptor-positive (HR+) and human epidermal growth factor receptor-negative (HER-2-) breast cancer progression. palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 33541289-9 2021 Patients treated with nab-paclitaxel had better event-free survival (EFS; HR = 0.69, 95%CI: 0.57-0.85, P < 0.001) than with sb-taxanes. nab 22-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-76 33541289-9 2021 Patients treated with nab-paclitaxel had better event-free survival (EFS; HR = 0.69, 95%CI: 0.57-0.85, P < 0.001) than with sb-taxanes. Paclitaxel 26-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-76 33246021-0 2021 Alpelisib Plus Fulvestrant for PIK3CA-Mutated, Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor-2-Negative Advanced Breast Cancer: Final Overall Survival Results From SOLAR-1. Alpelisib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-63 33495599-0 2021 CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers. Estrone 40-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-102 33495599-0 2021 CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers. Progesterone 53-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-102 33183970-0 2021 Final Efficacy Results of Neratinib in HER2-positive Hormone Receptor-positive Early-stage Breast Cancer From the Phase III ExteNET Trial. neratinib 26-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-69 33183970-1 2021 BACKGROUND: The ExteNET trial demonstrated improved invasive disease-free survival (iDFS) with neratinib, an irreversible pan-HER tyrosine kinase inhibitor, versus placebo in patients with human epidermal growth factor receptor 2-positive (HER2+)/hormone receptor-positive (HR+) early-stage breast cancer (eBC). neratinib 95-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 247-263 33388491-1 2021 PURPOSE: In the randomised phase II LEO trial, we investigated the effect of adding everolimus (EVE) to letrozole (LET) in ovarian-suppressed premenopausal women with hormone receptor-positive (HR+), HER2-negative (HER2-) recurrent/metastatic breast cancer. Everolimus 84-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 167-183 33460574-2 2021 The PALLAS trial aimed to investigate whether the addition of 2 years of palbociclib to adjuvant endocrine therapy improves invasive disease-free survival over endocrine therapy alone in patients with hormone-receptor-positive, HER2-negative, early-stage breast cancer. palbociclib 73-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 201-217 33421904-5 2021 Moreover, the role of Nur77 and NOR-1 in the regulation of Z-LIG-induced apoptosis and differentiation of AML cells was explored. ligustilide 59-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 22-27 33230905-0 2021 Everolimus plus exemestane treatment in metastatic hormone receptor-positive breast cancer patients previously treated with CDK4/6 inhibitor therapy. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 33230905-0 2021 Everolimus plus exemestane treatment in metastatic hormone receptor-positive breast cancer patients previously treated with CDK4/6 inhibitor therapy. exemestane 16-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 33230905-1 2021 BACKGROUND: The combination of everolimus (EVE) and exemestane (EXE) is approved for the treatment of metastatic hormone receptor-positive breast cancer (mHRBC) patients who progress on non-steroidal aromatase inhibitor (NSAI) therapy. Everolimus 31-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-129 33230905-1 2021 BACKGROUND: The combination of everolimus (EVE) and exemestane (EXE) is approved for the treatment of metastatic hormone receptor-positive breast cancer (mHRBC) patients who progress on non-steroidal aromatase inhibitor (NSAI) therapy. exemestane 52-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-129 33421904-0 2021 Z-Ligustilide Selectively Targets AML by Restoring Nuclear Receptors Nur77 and NOR-1-mediated Apoptosis and Differentiation. ligustilide 0-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-74 33421904-8 2021 Importantly, Z-LIG restored Nur77 and NOR-1 expression in AML cells by increasing Ace-H3 (lys9/14) enrichment in their promoters. ligustilide 13-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 33421904-4 2021 The anti-AML activity of Z-LIG was evaluated in vitro and in vivo, and the effect and underlying mechanisms of Z-LIG on the restoration of Nur77 and NOR-1 was determined. ligustilide 111-116 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 33421904-9 2021 Meanwhile, Z-LIG enhanced the recruitment of p300 and reduced the recruitment of HDAC1, HDAC4/5/7, and MTA1 in the Nur77 promoter and enhanced the recruitment of p-CREB and reduced HDAC1 and HDAC3 in the NOR-1 promoter. ligustilide 11-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-120 33421904-10 2021 Furthermore, Z-LIG-induced apoptosis was shown to be correlated with the mitochondria localization of Nur77/NOR-1 and subsequent Bcl-2 conformational change, converting Bcl-2 from a cyto-protective phenotype into a cyto-destructive phenotype. ligustilide 13-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-107 33421904-11 2021 Z-LIG-promoted differentiation was found to be related to Nur77/NOR-1-mediated myeloid differentiation-associated transcription factors Jun B, c-Jun, and C/EBPbeta. ligustilide 0-5 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-63 33514405-0 2021 Patterns of treatment with everolimus exemestane in hormone receptor-positive HER2-negative metastatic breast cancer in the era of targeted therapy. everolimus exemestane 27-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-68 33504001-4 2021 Palbociclib-resistant cells were generated by exposing hormone receptor-positive breast cancer cell lines to palbociclib. palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 55-71 33520003-7 2021 Results from BYLieve supports the notion that the combination of endocrine therapy with the PIK3Ca inhibitor alpelisib is a reasonable treatment approach in hormone-receptor positive/HER2-negative BC after prior CDK4/6-inhibitor therapy. Alpelisib 109-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-173 33473115-5 2021 Moreover, natural compound, salidroside effectively abrogates nicotine-induced neutrophil polarization and consequently reduced lung metastasis of hormone receptor-negative breast cancer cells. rhodioloside 28-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 147-163 33473115-5 2021 Moreover, natural compound, salidroside effectively abrogates nicotine-induced neutrophil polarization and consequently reduced lung metastasis of hormone receptor-negative breast cancer cells. Nicotine 62-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 147-163 33245358-0 2020 beta-glucan from Lentinus edodes inhibits breast cancer progression via the Nur77/HIF-1alpha axis. beta-Glucans 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-81 33552547-2 2021 Materials & methods: We analyzed the efficacy of treatment with bevacizumab plus paclitaxel in 43 patients with hormone receptor-positive and HER2-negative metastatic breast cancer. Paclitaxel 81-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-128 32718997-1 2021 PURPOSE: This study reports the maximum tolerated dose (MTD), recommended phase 2 dose (RP2D), and preliminary efficacy of alpelisib or buparlisib used in combination with tamoxifen plus goserelin in premenopausal patients with hormone receptor-positive (HR+), human epidermal growth factor receptor-2-negative (HER2-) advanced breast cancer (ABC). Alpelisib 123-132 nuclear receptor subfamily 4 group A member 1 Homo sapiens 228-244 33337350-10 2021 The relationship between miR-486-5p and NEAT1 or NR4A1 was confirmed by dual-luciferase reporter assay. mir-486-5p 25-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-54 33447040-1 2020 Background: Clinical studies have shown that palbociclib improves progression-free survival in hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2-) patients with advanced breast cancer (ABC). palbociclib 45-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 95-111 32328775-4 2021 METHODS: We proposed a prospective trial to measure the change in blood estradiol levels in postmenopausal women with hormone receptor-positive breast cancer undergoing treatment with aromatase inhibitors when treated with vaginal estrogen preparation, Estring, for their urogenital symptoms. Estradiol 72-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-134 32358778-1 2021 PURPOSE: To assess the feasibility and efficacy of a non-hormonal hyaluronic acid (HLA) vaginal gel in improving vulvovaginal estrogen-deprivation symptoms in postmenopausal women with a history of hormone receptor-positive (HR+) cancer. Hyaluronic Acid 83-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 198-214 33242757-1 2020 BACKGROUND: Palbociclib is indicated for the treatment of hormone receptor-positive (HR+), HER2-negative (HER2-) advanced breast cancer (ABC), in combination with endocrine therapy. palbociclib 12-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-74 32926316-1 2020 The primary and secondary benefits of tamoxifen as adjuvant therapy in women with hormone-receptor-positive breast cancer are substantial: a 1% decrease in the risk of death each year for 10 years with each additional year of treatment during the first 5 years. Tamoxifen 38-47 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-98 33336619-2 2020 We explored the conjugation of riboflavin (RF) ligand from the end of the ribityl chain (N-10) to the polymer strands as well as from the amine group on the isoalloxazine head (N-3). Riboflavin 31-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-93 33336619-2 2020 We explored the conjugation of riboflavin (RF) ligand from the end of the ribityl chain (N-10) to the polymer strands as well as from the amine group on the isoalloxazine head (N-3). Riboflavin 43-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-93 33336619-5 2020 The introduction of RF from the N-10 position in any composition has increased the energy level of nanocarriers. Riboflavin 20-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-36 33336619-7 2020 Furthermore, with N-10 samples based on both polymers, non-targeted models form the stablest particles in each category. Polymers 45-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-22 33336619-8 2020 These findings are further confirmed with molecular docking analysis which revealed affinity energy of RF toward polymer chain from N-3 and N-10 are -981.57 kJ/mole and -298.23 kJ/mole, respectively. Polymers 113-120 nuclear receptor subfamily 4 group A member 1 Homo sapiens 140-144 33408886-0 2020 Tryptophanyl-tRNA Synthetase Sensitizes Hormone Receptor-Positive Breast Cancer to Docetaxel-Based Chemotherapy. Docetaxel 83-92 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-56 32946924-0 2020 Sacituzumab Govitecan in Previously Treated Hormone Receptor-Positive/HER2-Negative Metastatic Breast Cancer: Final Results from a Phase 1/2, Single-Arm, Basket Trial. govitecan 12-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-60 32888142-0 2020 Luminal subtypes and response to neoadjuvant chemotherapy for hormone receptor-positive HER2-negative patients. Phenobarbital 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-78 32881420-3 2020 With the recent FDA approval of alpelisib for the treatment of PIK3CA-mutated hormone-receptor positive metastatic breast cancer, tumor molecular profiling to identify somatic mutations and potential molecularly targeted agents is increasingly utilized in the treatment of advanced breast cancer. Alpelisib 32-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-94 32962980-0 2020 A prognostic model based on PAM50 and clinical variables (PAM50MET) for metastatic hormone-receptor-positive HER2-negative breast cancer. pam50met 58-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-99 32988969-1 2020 PURPOSE: Determine if the androgen receptor (AR) inhibitor enzalutamide improves effectiveness of endrocrine therapy (ET) in hormone receptor-positive (HR+) breast cancer. endrocrine 98-108 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 33022852-1 2020 Fulvestrant 500 mg is standard of care for endocrine therapy-naive or pretreated women with hormone receptor-positive (HR+) metastatic breast cancer (MBC). Fulvestrant 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-108 32988969-0 2020 A Randomized Placebo-Controlled Phase 2 Trial Evaluating Exemestane With or Without Enzalutamide in Patients With Hormone Receptor-positive Breast Cancer. exemestane 57-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-130 32988969-1 2020 PURPOSE: Determine if the androgen receptor (AR) inhibitor enzalutamide improves effectiveness of endrocrine therapy (ET) in hormone receptor-positive (HR+) breast cancer. enzalutamide 59-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 33247224-9 2020 Further study is required to clarify the molecular mechanisms of tubal metaplasia and the expression loss of hormone receptor in the endometrium as a result of MEA treatment. Cysteamine 160-163 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-125 32459035-0 2020 A Phase II Prospective, Randomized, Double-Blind, Placebo-Controlled and Multicenter Clinical Trial to Assess the Safety of 0.005% Estriol Vaginal Gel in Hormone Receptor-Positive Postmenopausal Women With Early Stage Breast Cancer in Treatment With Aromatase Inhibitor in the Adjuvant Setting. Estriol 131-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-170 33151471-1 2020 BACKGROUND: Everolimus plus exemestane is approved for the treatment of hormone receptor-positive metastatic breast cancer (MBC) after progression on nonsteroidal aromatase inhibitors. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-88 33151471-1 2020 BACKGROUND: Everolimus plus exemestane is approved for the treatment of hormone receptor-positive metastatic breast cancer (MBC) after progression on nonsteroidal aromatase inhibitors. exemestane 28-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-88 33151471-13 2020 CONCLUSIONS: Everolimus reduces the risk of disease progression in hormone receptor (+) MBC. Everolimus 13-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-83 33324567-1 2020 Background: Tamoxifen and fulvestrant, both approved for endocrine therapy, have remarkably increased the prognosis of hormone receptor-positive breast cancer patients. Tamoxifen 12-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-135 33324567-1 2020 Background: Tamoxifen and fulvestrant, both approved for endocrine therapy, have remarkably increased the prognosis of hormone receptor-positive breast cancer patients. Fulvestrant 26-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-135 33198673-0 2020 Utility of 18F-FDG PET/CT for predicting pathologic complete response in hormone receptor-positive, HER2-negative breast cancer patients receiving neoadjuvant chemotherapy. Fluorodeoxyglucose F18 11-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 73-89 32770287-0 2020 Immune system and angiogenesis-related potential surrogate biomarkers of response to everolimus-based treatment in hormone receptor-positive breast cancer: an exploratory study. Everolimus 85-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-131 33172112-6 2020 We observed that knockdown of NR4A1 dramatically increased isoharringtonine-induced cancer cell death in A549 tumorspheroids by activating the intrinsic apoptosis pathway. isoharringtonine 59-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-35 32770287-1 2020 PURPOSE: mTOR inhibitor everolimus is used for hormone receptor-positive (HR+)/HER2-negative metastatic breast cancer (mBC). Everolimus 24-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-63 32803637-18 2020 CONCLUSIONS: Important changes occurred in EBC treatment, particularly for hormone receptor-positive tumors, as the outbreak progressed in each region. NSC638702 43-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 32787449-3 2020 Female and male patients in the USA and Canada diagnosed with hormone receptor-positive/HER2-negative metastatic breast cancer were enrolled in the study and treated with the cyclin-dependent kinase 4/6 inhibitor palbociclib when hormone receptor-positive/HER2-negative metastatic breast cancer was deemed to be indicated by their physician. palbociclib 213-224 nuclear receptor subfamily 4 group A member 1 Homo sapiens 230-246 32170637-1 2020 BACKGROUND: The addition of everolimus to exemestane therapy significantly improves progression-free survival in postmenopausal patients with hormone-receptor (HR)-positive HER2-negative endocrine-resistant breast cancer. Everolimus 28-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 142-158 33154825-0 2020 Clinical Implications of Serum 25-Hydroxyvitamin D Status after 5-Year Adjuvant Endocrine Therapy for Late Recurrence of Hormone Receptor-positive Breast Cancer. 25-hydroxyvitamin D 31-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-137 32717483-0 2020 Design, synthesis, and biological evaluation of 5-((8-methoxy-2-methylquinolin-4-yl)amino)-1H-indole-2-carbohydrazide derivatives as novel Nur77 modulators. 5-((8-methoxy-2-methylquinolin-4-yl)amino)-1h-indole-2-carbohydrazide 48-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 32717483-2 2020 Herein, we detailed the discovery of a novel series of 5-((8-methoxy-2-methylquinolin-4-yl)amino)-1H-indole-2-carbohydrazide derivatives as potential Nur77 modulators. 5-((8-methoxy-2-methylquinolin-4-yl)amino)-1h-indole-2-carbohydrazide 55-124 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-155 32170637-1 2020 BACKGROUND: The addition of everolimus to exemestane therapy significantly improves progression-free survival in postmenopausal patients with hormone-receptor (HR)-positive HER2-negative endocrine-resistant breast cancer. Everolimus 28-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-162 32170637-1 2020 BACKGROUND: The addition of everolimus to exemestane therapy significantly improves progression-free survival in postmenopausal patients with hormone-receptor (HR)-positive HER2-negative endocrine-resistant breast cancer. exemestane 42-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 142-158 32170637-1 2020 BACKGROUND: The addition of everolimus to exemestane therapy significantly improves progression-free survival in postmenopausal patients with hormone-receptor (HR)-positive HER2-negative endocrine-resistant breast cancer. exemestane 42-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-162 33046982-0 2020 Efficacy and Safety of Fulvestrant 500mg in Hormone-receptor Positive Human Epidermal Receptor 2 Negative Advanced Breast Cancer: A Real-world Study in China. Fulvestrant 23-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-60 32831911-7 2020 The hormone receptor (HR) status and number of metastases were significant influencing factors of PFS in the BOM group. bom 109-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-20 32831911-7 2020 The hormone receptor (HR) status and number of metastases were significant influencing factors of PFS in the BOM group. bom 109-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 22-24 32831911-8 2020 Furthermore, the HR status, location of bone metastasis and number of bone metastases were significantly associated with OS of patients in the BOM group. bom 143-146 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-19 32831911-11 2020 In the non-BOM group, patients with HR+/HER2- and HER2+ tumors had improved prognosis. bom 11-14 nuclear receptor subfamily 4 group A member 1 Homo sapiens 36-38 32831911-16 2020 HR- and multiple bone metastases, as well as combined axial and appendicular bone metastases, were significantly associated with poor prognosis in the patients with BOM. bom 165-168 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-2 32957311-11 2020 CONCLUSIONS: Our study suggested that aspirin use might be associated with a reduced risk of breast cancer, particularly for reducing the risk of hormone receptor positive tumors or in situ breast tumors, and the risk of breast cancer in postmenopausal women. Aspirin 38-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 146-162 32951520-1 2021 PURPOSE: Exemestane, a steroidal aromatase inhibitor, is an important therapeutic option in the treatment of post-menopausal hormone receptor positive breast cancer. exemestane 9-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 32934206-1 2020 Palbociclib, a CDK4/6 inhibitor, has been granted accelerated approval by US FDA for hormone receptor-positive HER2-negative metastatic breast cancer. palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 32586939-0 2020 Clinical significance of circulating tumor cells in hormone receptor-positive metastatic breast cancer patients who received letrozole with or without bevacizumab. Letrozole 125-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-68 32661666-0 2020 Correction to: Palbociclib use with grade 3 neutropenia in hormone receptor-positive metastatic breast cancer. palbociclib 15-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-75 32671612-0 2020 Impact of early dose intensity reduction of Palbociclib on clinical outcomes in patients with hormone-receptor-positive metastatic breast cancer. palbociclib 44-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-110 32614992-2 2020 METHODS: Women with hormone receptor-positive BC who were taking AET completed standardized surveys about their health-related QOL, AET-related symptoms, and levels of PA using validated measures. 2-(2-Aminoethyl)isothiourea dihydrobromide 65-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-36 32463152-0 2020 A phase II trial of cabozantinib in hormone-receptor positive breast cancer with bone metastases. cabozantinib 20-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 36-52 32868353-0 2020 Half-dose fulvestrant plus anastrozole as a first-line treatment for hormone receptor-positive metastatic breast cancer: a cost-effectiveness analysis. Fulvestrant 10-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 32868353-0 2020 Half-dose fulvestrant plus anastrozole as a first-line treatment for hormone receptor-positive metastatic breast cancer: a cost-effectiveness analysis. Anastrozole 27-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 32868353-1 2020 OBJECTIVE: The S0226 trial demonstrated that the combination of half-dose fulvestrant (FUL) and anastrozole (ANA) (F&A) caused a significant improvement in overall survival (OS) versus ANA monotherapy for first-line treatment of postmenopausal women with hormone receptor-positive metastatic breast cancer (PMW-MBC (HR+)). Fulvestrant 74-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 255-271 32868353-1 2020 OBJECTIVE: The S0226 trial demonstrated that the combination of half-dose fulvestrant (FUL) and anastrozole (ANA) (F&A) caused a significant improvement in overall survival (OS) versus ANA monotherapy for first-line treatment of postmenopausal women with hormone receptor-positive metastatic breast cancer (PMW-MBC (HR+)). Fulvestrant 87-90 nuclear receptor subfamily 4 group A member 1 Homo sapiens 255-271 32868353-1 2020 OBJECTIVE: The S0226 trial demonstrated that the combination of half-dose fulvestrant (FUL) and anastrozole (ANA) (F&A) caused a significant improvement in overall survival (OS) versus ANA monotherapy for first-line treatment of postmenopausal women with hormone receptor-positive metastatic breast cancer (PMW-MBC (HR+)). Anastrozole 96-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 255-271 32868353-1 2020 OBJECTIVE: The S0226 trial demonstrated that the combination of half-dose fulvestrant (FUL) and anastrozole (ANA) (F&A) caused a significant improvement in overall survival (OS) versus ANA monotherapy for first-line treatment of postmenopausal women with hormone receptor-positive metastatic breast cancer (PMW-MBC (HR+)). Anastrozole 109-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 255-271 32868353-1 2020 OBJECTIVE: The S0226 trial demonstrated that the combination of half-dose fulvestrant (FUL) and anastrozole (ANA) (F&A) caused a significant improvement in overall survival (OS) versus ANA monotherapy for first-line treatment of postmenopausal women with hormone receptor-positive metastatic breast cancer (PMW-MBC (HR+)). Fluorine 87-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 255-271 33014129-0 2020 Erratum: RENATA study-Latin American prospective experience: clinical outcome of patients treated with palbociclib in hormone receptor-positive metastatic breast cancer-real-world use. palbociclib 103-114 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-134 32335491-0 2020 Safety and efficacy of sirolimus combined with endocrine therapy in patients with advanced hormone receptor-positive breast cancer and the exploration of biomarkers. Sirolimus 23-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-107 32335491-1 2020 BACKGROUND: We performed a retrospective study on the efficacy and safety of sirolimus (an mTOR inhibitor) in hormone receptor (HR)-positive advanced breast cancer and searched for biomarkers to predict its efficacy. Sirolimus 77-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-126 32335491-1 2020 BACKGROUND: We performed a retrospective study on the efficacy and safety of sirolimus (an mTOR inhibitor) in hormone receptor (HR)-positive advanced breast cancer and searched for biomarkers to predict its efficacy. Sirolimus 77-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 128-130 32335491-2 2020 METHODS: All patients with HR-positive metastatic breast cancer treated with sirolimus plus endocrine therapy between December 2017 and July 2018 at the Cancer Hospital, Chinese Academy of Medical Sciences were consecutively and retrospectively reviewed. Sirolimus 77-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-29 32335491-11 2020 CONCLUSIONS: Sirolimus is a potentially effective treatment option for patients with HR-positive advanced breast cancer. Sirolimus 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-87 32052382-1 2020 PURPOSE: Hormone receptor (HR)-positive, Human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer (MBC) requires a therapeutic approach that takes into account multiple factors, with treatment being based on anti-estrogen hormone therapy (HT). Estrogens 238-246 nuclear receptor subfamily 4 group A member 1 Homo sapiens 9-25 32052382-1 2020 PURPOSE: Hormone receptor (HR)-positive, Human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer (MBC) requires a therapeutic approach that takes into account multiple factors, with treatment being based on anti-estrogen hormone therapy (HT). Estrogens 238-246 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-29 32982739-0 2020 Cantharidin Induces Apoptosis and Promotes Differentiation of AML Cells Through Nuclear Receptor Nur77-Mediated Signaling Pathway. Cantharidin 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-102 32905449-0 2020 Bis-indole derived nuclear receptor 4A1 (NR4A1) antagonists inhibit TGFbeta-induced invasion of embryonal rhabdomyosarcoma cells. bis-indole 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-39 32905449-0 2020 Bis-indole derived nuclear receptor 4A1 (NR4A1) antagonists inhibit TGFbeta-induced invasion of embryonal rhabdomyosarcoma cells. bis-indole 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 32905449-2 2020 This response is inhibited by the NR4A1 antagonist 1,1-bis(3"-indoly)-1-(p-hydroxyphenyl) methane (CDIM8) and we hypothesized that similar effects would be observed in Rhabdomyosarcoma (RMS) cells. 1,1-bis(3"-indoly)-1-(p-hydroxyphenyl) methane 51-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-39 32905449-2 2020 This response is inhibited by the NR4A1 antagonist 1,1-bis(3"-indoly)-1-(p-hydroxyphenyl) methane (CDIM8) and we hypothesized that similar effects would be observed in Rhabdomyosarcoma (RMS) cells. DIM-C-pPhOH 99-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-39 32905449-7 2020 The novel mechanism of CDIM8-mediated inhibition of basal and TGFbeta-induced ERMS cell invasion was due to activation of the Bcl-2-NR4A1 complex, mitochondrial disruption, induction of the tumor suppressor-like cytokine interleukin-24 (IL-24) which in turn downregulates beta-catenin expression. DIM-C-pPhOH 23-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-137 32577940-0 2020 Palbociclib use with grade 3 neutropenia in hormone receptor-positive metastatic breast cancer. palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-60 32463152-1 2020 BACKGROUND: We assessed the antitumor activity of cabozantinib, a potent multi-receptor oral tyrosine kinase inhibitor, in patients with hormone-receptor positive breast cancer with bone metastases. cabozantinib 50-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-153 32728620-3 2020 The patient is a 37-year-old woman with recurrent, hormone receptor-positive, HER2-negative MBC that had progressed despite hormonal therapy and palbociclib. palbociclib 145-156 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 32756099-1 2020 RATIONALE: Within a rapidly expanding therapeutic armamentarium, the combination of everolimus (Eve) plus exemestane (Exe) utility needs to be reinstated in hormone receptor positive (HR+), human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer (MBC). Everolimus 84-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-173 32756099-1 2020 RATIONALE: Within a rapidly expanding therapeutic armamentarium, the combination of everolimus (Eve) plus exemestane (Exe) utility needs to be reinstated in hormone receptor positive (HR+), human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer (MBC). exemestane 106-116 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-173 32732875-3 2020 We demonstrate that mammary tumors driven by medroxyprogesterone acetate (M) and 7,12-dimethylbenz[a]anthracene (D) recapitulate several key features of human luminal B HR+HER2- BC, including limited immune infiltration and poor sensitivity to ICBs. Medroxyprogesterone Acetate 45-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 169-171 32732875-3 2020 We demonstrate that mammary tumors driven by medroxyprogesterone acetate (M) and 7,12-dimethylbenz[a]anthracene (D) recapitulate several key features of human luminal B HR+HER2- BC, including limited immune infiltration and poor sensitivity to ICBs. 9,10-Dimethyl-1,2-benzanthracene 81-111 nuclear receptor subfamily 4 group A member 1 Homo sapiens 169-171 32708154-0 2020 12-Deacetyl-12-epi-Scalaradial, a Scalarane Sesterterpenoid from a Marine Sponge Hippospongia sp., Induces HeLa Cells Apoptosis via MAPK/ERK Pathway and Modulates Nuclear Receptor Nur77. 12-deacetyl-12-epi 0-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 180-185 32753876-0 2020 Outcome of Everolimus-Based Therapy in Hormone-Receptor-Positive Metastatic Breast Cancer Patients After Progression on Palbociclib. Everolimus 11-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-55 32753876-0 2020 Outcome of Everolimus-Based Therapy in Hormone-Receptor-Positive Metastatic Breast Cancer Patients After Progression on Palbociclib. palbociclib 120-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-55 32753876-1 2020 Background: Despite the approval of mTOR inhibitor everolimus and CDK4/6 inhibitors in the management of hormone-receptor-positive HER2 non-amplified metastatic breast cancer (HR+ HER2-MBC), the optimal sequence of therapy is unclear. Everolimus 51-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-121 32708154-7 2020 The dual-luciferase reporter assays suggested that 12-deacetyl-12-epi-scalaradial could selectively enhance the trans-activation activity of Nur77. 12-deacetyl-12-epi-scalaradial 51-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 141-146 32708154-8 2020 Furthermore, Western blotting analysis and fluorescence quenching showed that 12-deacetyl-12-epi-scalaradial could induce the phosphorylation of Nur77 and interact with the ligand-binding domain (LBD) of Nur77. 12-deacetyl-12-epi 78-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-150 32708154-8 2020 Furthermore, Western blotting analysis and fluorescence quenching showed that 12-deacetyl-12-epi-scalaradial could induce the phosphorylation of Nur77 and interact with the ligand-binding domain (LBD) of Nur77. 12-deacetyl-12-epi 78-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 204-209 32708154-9 2020 Our research confirmed 12-deacetyl-12-epi-scalaradial as a potential agent for cervical cancer therapy and provided a view that 12-deacetyl-12-epi-scalaradial may be a modulator of Nur77. 12-deacetyl-12-epi 128-146 nuclear receptor subfamily 4 group A member 1 Homo sapiens 181-186 32660609-0 2020 Pyrotinib with trastuzumab and aromatase inhibitors as first-line treatment for HER2 positive and hormone receptor positive metastatic or locally advanced breast cancer: study protocol of a randomized controlled trial. pyrotinib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 98-114 32575989-0 2020 Bipentazole (N10): A Low-Energy Molecular Nitrogen Allotrope with High Intrinsic Stability. bipentazole 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-17 32575989-0 2020 Bipentazole (N10): A Low-Energy Molecular Nitrogen Allotrope with High Intrinsic Stability. Nitrogen 42-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-17 32575989-1 2020 In this letter, we report a crystal structure prediction and characterization of a molecular nitrogen allotrope N10 (bipentazole) using state-of-the-art computational methods. Nitrogen 93-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-115 32575989-1 2020 In this letter, we report a crystal structure prediction and characterization of a molecular nitrogen allotrope N10 (bipentazole) using state-of-the-art computational methods. bipentazole 117-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-115 32367072-13 2020 After adjustment for prognostic factors, we found that tamoxifen was found to reduce the recurrence rate by 68% (hazard ratio HR = 0.32; 95% confidence interval, CI: 0.14-0.74). Tamoxifen 55-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-128 32760629-3 2020 Here, we present a case report of pneumonitis as a rare side effect of palbociclib in the treatment of metastatic hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (ERBB2-) breast cancer in addition to endocrine therapy. palbociclib 71-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-130 32352244-0 2020 Buparlisib in combination with tamoxifen in pretreated patients with hormone receptor-positive, HER2-negative advanced breast cancer molecularly stratified for PIK3CA mutations and loss of PTEN expression. NVP-BKM120 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 32352244-0 2020 Buparlisib in combination with tamoxifen in pretreated patients with hormone receptor-positive, HER2-negative advanced breast cancer molecularly stratified for PIK3CA mutations and loss of PTEN expression. Tamoxifen 31-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 32385792-0 2020 Association of CYP19A1 gene variations with adjuvant letrozole-induced adverse events in South Indian postmenopausal breast cancer cohort expressing hormone-receptor positivity. Letrozole 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-165 32385792-3 2020 Therefore, we aimed to determine whether SNPs in the CYP19A1 gene are associated with adjuvant letrozole-induced "specific" AEs in postmenopausal hormone receptor-positive (HR+) breast cancer patients. Letrozole 95-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 146-162 31773503-17 2020 CONCLUSION: The standard treatment of hormone receptor positive and HER-2 negative metastatic breast cancer is everolimus together with exemestane. Everolimus 111-121 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-54 31773503-17 2020 CONCLUSION: The standard treatment of hormone receptor positive and HER-2 negative metastatic breast cancer is everolimus together with exemestane. exemestane 136-146 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-54 31993850-0 2020 Lactate accelerates vascular calcification through NR4A1-regulated mitochondrial fission and BNIP3-related mitophagy. Lactic Acid 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-56 32636632-1 2020 Background: Fulvestrant (FUL) and the combination of everolimus and exemestane (EVE-EXE) were the options to treat hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer (MBC) patients who were refractory to aromatase inhibitors (AIs). exemestane 68-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-131 32637176-2 2020 Recent evidence suggests combination therapy with the PI3K inhibitor (PI3Ki) alpelisib and endocrine therapy (ET) improves response rates and progression-free survival (PFS) in PIK3CA-mutant, hormone receptor positive (HR+) BC versus ET alone; thus, better understanding the clinical and epidemiologic elements of these mutations is warranted. Alpelisib 77-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 192-208 32570839-5 2020 In contrast, RO4929097 downregulated the NOTCH3/NR4A1 axis and counteracted the spontaneous and gliotoxin-induced apoptosis. 2,2-dimethyl-N-(6-oxo-6,7-dihydro-5H-dibenzo(b,d)azepin-7-yl)-N'-(2,2,3,3,3-pentafluoropropyl)malonamide 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 32549380-6 2020 This lower prevalence of HER2-positive in-screen-detected breast carcinomas was observed in both hormone receptor positive (luminal HER2) and hormone-receptor-negative (HER2 enriched) tumors. Phenobarbital 124-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-113 31993850-7 2020 In VSMCs, lactate increased NR4A1 expression, leading to activation of DNA-PKcs and p53. Lactic Acid 10-17 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 31993850-8 2020 Lactate induced Drp1 migration to the mitochondria and enhanced mitochondrial fission through NR4A1. Lactic Acid 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 31993850-11 2020 The excessive fission and deficient mitophagy damaged mitochondrial structure and impaired respiratory function, determined by mPTP opening rate, mitochondrial membrane potential, mitochondrial morphology under TEM, ATP production, and OCR, which was reversed by NR4A1 silencing. Adenosine Triphosphate 216-219 nuclear receptor subfamily 4 group A member 1 Homo sapiens 263-268 31993850-12 2020 Mechanistically, lactate enhanced fission but halted mitophagy via activation of the NR4A1/DNA-PKcs/p53 pathway, evoking apoptosis, finally accelerating osteoblastic phenotype transition of VSMC and calcium deposition. Lactic Acid 17-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-90 31993850-13 2020 This study suggests that the NR4A1/DNA-PKcs/p53 pathway is involved in the mechanism by which lactate accelerates vascular calcification, partly through excessive Drp-mediated mitochondrial fission and BNIP3-related mitophagy deficiency. Lactic Acid 94-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-34 32147404-8 2020 After multivariable logistic regression analysis, variables that were associated with ALN metastasis were palpability, multifocality, location, size, histologic type, grade, lymphovascular invasion, hormone receptor expression, and Ki-67 level. aln 86-89 nuclear receptor subfamily 4 group A member 1 Homo sapiens 199-215 32279525-5 2020 Several clinical trials are underway to develop treatment strategies based on shortterm responsiveness to NAE to improve the prognosis of hormone receptor (HR)-positive/HER2-negative breast cancer. N-lauroylethanolamine 106-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 138-160 32541183-1 2020 An 89-year-old woman with recurrent hormone receptor-positive and HER2-negative breast cancer was treated with fulvestrant-palbociclib combination therapy. Fulvestrant 111-122 nuclear receptor subfamily 4 group A member 1 Homo sapiens 36-52 32060781-1 2020 PURPOSE: To examine (1) the trend and associated factors of Oncotype DX (ODX) use among hormone receptor-positive (HR+) breast cancer (BC) patients in 2004-2015; (2) the trend of reported chemotherapy by Recurrence Score (RS); and (3) the survival differences associated with ODX use. odx 73-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-104 32458702-0 2020 Neratinib for the treatment of early-stage, hormone receptor-positive, HER2-overexpressed breast cancer. neratinib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-60 32257203-0 2020 Palbociclib added to ongoing endocrine therapy for hormone receptor-positive HER2-negative metastatic breast cancer: A case report series. palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 32257203-7 2020 The hypothesis that a selected subpopulation of patients with HR+/HER2- metastatic breast cancer may benefit from the addition of palbociclib to ongoing endocrine therapy beyond disease progression merits further investigation. palbociclib 130-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-64 32326897-0 2020 Different associations of tumor PIK3CA mutations and clinical outcomes according to aspirin use among women with metastatic hormone receptor positive breast cancer. Aspirin 84-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 124-140 31618131-1 2020 PURPOSE: The Tamoxifen and Exemestane Trial (TEXT)/Suppression of Ovarian Function Trial (SOFT) showed superior outcomes for premenopausal women with hormone receptor (HR)-positive breast cancer treated with adjuvant exemestane plus ovarian function suppression (OFS) or tamoxifen plus OFS versus tamoxifen alone. Tamoxifen 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-166 31618131-1 2020 PURPOSE: The Tamoxifen and Exemestane Trial (TEXT)/Suppression of Ovarian Function Trial (SOFT) showed superior outcomes for premenopausal women with hormone receptor (HR)-positive breast cancer treated with adjuvant exemestane plus ovarian function suppression (OFS) or tamoxifen plus OFS versus tamoxifen alone. Tamoxifen 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 168-170 31618131-1 2020 PURPOSE: The Tamoxifen and Exemestane Trial (TEXT)/Suppression of Ovarian Function Trial (SOFT) showed superior outcomes for premenopausal women with hormone receptor (HR)-positive breast cancer treated with adjuvant exemestane plus ovarian function suppression (OFS) or tamoxifen plus OFS versus tamoxifen alone. exemestane 27-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-166 31618131-1 2020 PURPOSE: The Tamoxifen and Exemestane Trial (TEXT)/Suppression of Ovarian Function Trial (SOFT) showed superior outcomes for premenopausal women with hormone receptor (HR)-positive breast cancer treated with adjuvant exemestane plus ovarian function suppression (OFS) or tamoxifen plus OFS versus tamoxifen alone. exemestane 27-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 168-170 31618131-1 2020 PURPOSE: The Tamoxifen and Exemestane Trial (TEXT)/Suppression of Ovarian Function Trial (SOFT) showed superior outcomes for premenopausal women with hormone receptor (HR)-positive breast cancer treated with adjuvant exemestane plus ovarian function suppression (OFS) or tamoxifen plus OFS versus tamoxifen alone. Tamoxifen 271-280 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-166 31618131-1 2020 PURPOSE: The Tamoxifen and Exemestane Trial (TEXT)/Suppression of Ovarian Function Trial (SOFT) showed superior outcomes for premenopausal women with hormone receptor (HR)-positive breast cancer treated with adjuvant exemestane plus ovarian function suppression (OFS) or tamoxifen plus OFS versus tamoxifen alone. Tamoxifen 271-280 nuclear receptor subfamily 4 group A member 1 Homo sapiens 168-170 31618131-1 2020 PURPOSE: The Tamoxifen and Exemestane Trial (TEXT)/Suppression of Ovarian Function Trial (SOFT) showed superior outcomes for premenopausal women with hormone receptor (HR)-positive breast cancer treated with adjuvant exemestane plus ovarian function suppression (OFS) or tamoxifen plus OFS versus tamoxifen alone. Tamoxifen 297-306 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-166 32008124-0 2020 Anastrozole plus fulvestrant vs. anastrozole alone for hormone receptor-positive advanced breast cancer: a meta-analysis of randomized controlled trials. anastrozole 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 55-71 32008124-0 2020 Anastrozole plus fulvestrant vs. anastrozole alone for hormone receptor-positive advanced breast cancer: a meta-analysis of randomized controlled trials. ici 182,780 17-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 55-71 31853795-0 2020 First-line fulvestrant plus anastrozole for hormone-receptor-positive metastatic breast cancer in postmenopausal women: a cost-effectiveness analysis. Anastrozole 28-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-60 31853795-1 2020 PURPOSE: In a recent randomized, open-label trial (S0226), the addition of fulvestrant to anastrozole therapy decreased the risk of progression and death in patients with hormone-receptor-positive metastatic breast cancer. Anastrozole 90-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-187 31618131-1 2020 PURPOSE: The Tamoxifen and Exemestane Trial (TEXT)/Suppression of Ovarian Function Trial (SOFT) showed superior outcomes for premenopausal women with hormone receptor (HR)-positive breast cancer treated with adjuvant exemestane plus ovarian function suppression (OFS) or tamoxifen plus OFS versus tamoxifen alone. Tamoxifen 297-306 nuclear receptor subfamily 4 group A member 1 Homo sapiens 168-170 31618131-11 2020 CONCLUSION: Premenopausal women with HR-positive/HER2-negative breast cancer and high recurrence risk, as defined by clinicopathologic characteristics, may experience a 10% to 15% absolute improvement in 8-year freedom from distant recurrence with exemestane plus OFS versus tamoxifen plus OFS or tamoxifen alone. exemestane 248-258 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-39 31618131-11 2020 CONCLUSION: Premenopausal women with HR-positive/HER2-negative breast cancer and high recurrence risk, as defined by clinicopathologic characteristics, may experience a 10% to 15% absolute improvement in 8-year freedom from distant recurrence with exemestane plus OFS versus tamoxifen plus OFS or tamoxifen alone. Tamoxifen 275-284 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-39 31618131-11 2020 CONCLUSION: Premenopausal women with HR-positive/HER2-negative breast cancer and high recurrence risk, as defined by clinicopathologic characteristics, may experience a 10% to 15% absolute improvement in 8-year freedom from distant recurrence with exemestane plus OFS versus tamoxifen plus OFS or tamoxifen alone. Tamoxifen 297-306 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-39 32183517-1 2020 We report the first time resolved resonant Raman (TR3) spectra of photo-induced charge transfer from \RuII\ to methyl viologen, with observations of vibrational structure. Paraquat 111-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-53 32308485-2 2020 This study aims to evaluate the alternative application of Magee Equation 2 score in predicting pathological complete response (pCR) after neoadjuvant chemotherapy (NAC) in hormone receptor (HR)-positive, HER2-negative breast cancer. nac 165-168 nuclear receptor subfamily 4 group A member 1 Homo sapiens 173-189 32308485-2 2020 This study aims to evaluate the alternative application of Magee Equation 2 score in predicting pathological complete response (pCR) after neoadjuvant chemotherapy (NAC) in hormone receptor (HR)-positive, HER2-negative breast cancer. nac 165-168 nuclear receptor subfamily 4 group A member 1 Homo sapiens 191-193 32308485-13 2020 Conclusion: Among patients with HR-positive and HER2-negative breast cancer treated with NAC, Magee Equation 2 might be used as a tool for predicting the pCR and clinical outcome. nac 89-92 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-34 32675948-1 2020 The aim of this retrospective study was to assess the efficacy of topical hormonal therapy (THT) to relieve vaginal symptoms resulting from antihormonal therapy in women with hormone receptor-positive breast cancer. tetrahydrothiophene 92-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 175-191 32398983-1 2020 Tamoxifen is frequently used as adjuvant treatment in premenopausal patients with hormone receptor-positive early breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-98 31932237-0 2020 A Phase II Open Label Study of Everolimus in Combination With Endocrine Therapy in Resistant Hormone Receptor-Positive HER2-Negative Advanced Breast Cancer. everolimus 31-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-109 31932237-1 2020 BACKGROUND: Therapies targeting estrogen receptor signaling are standard for patients with hormone receptor (HR)-positive (HR+) metastatic breast cancer (MBC). Estrogens 32-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-107 31932237-1 2020 BACKGROUND: Therapies targeting estrogen receptor signaling are standard for patients with hormone receptor (HR)-positive (HR+) metastatic breast cancer (MBC). Estrogens 32-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-111 31932237-1 2020 BACKGROUND: Therapies targeting estrogen receptor signaling are standard for patients with hormone receptor (HR)-positive (HR+) metastatic breast cancer (MBC). Estrogens 32-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-125 31932237-3 2020 Addition of the mTOR inhibitor, everolimus, to exemestane doubled progression-free survival (PFS) in HR+/HER2- MBC patients whose disease had previously progressed during endocrine therapy. everolimus 32-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 101-103 31932237-3 2020 Addition of the mTOR inhibitor, everolimus, to exemestane doubled progression-free survival (PFS) in HR+/HER2- MBC patients whose disease had previously progressed during endocrine therapy. exemestane 47-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 101-103 31932237-4 2020 In this phase II study, we used everolimus in addition to the most recent endocrine therapy during which a patient"s disease progressed, in an attempt to restore and extend the benefit of the antiestrogen therapy in patients with HR+/HER2- MBC. everolimus 32-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 230-232 31932237-14 2020 CONCLUSION: After progression during antiestrogen therapy, the addition of everolimus, without changing the hormonal therapy, resulted in a median PFS of 6.6 months, suggesting efficacy in patients with HR+/HER2- MBC. everolimus 75-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 203-205 32099996-3 2020 Moreover, the treatment of these cells with bis-indole derived NR4A1 ligands 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) and its buttressed 3-chloro-5-methoxy analog (DIM-C-pPhOH-3-Cl-5-OCH3) inhibited cell growth and induced apoptosis and related genes. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 77-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 32099996-0 2020 BIS-INDOLE DERIVED NUCLEAR RECEPTOR 4A1 (NR4A1, Nur77) LIGANDS AS INHIBITORS OF ENDOMETRIOSIS. bis-indole 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-39 32099996-3 2020 Moreover, the treatment of these cells with bis-indole derived NR4A1 ligands 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) and its buttressed 3-chloro-5-methoxy analog (DIM-C-pPhOH-3-Cl-5-OCH3) inhibited cell growth and induced apoptosis and related genes. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 125-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 32099996-0 2020 BIS-INDOLE DERIVED NUCLEAR RECEPTOR 4A1 (NR4A1, Nur77) LIGANDS AS INHIBITORS OF ENDOMETRIOSIS. bis-indole 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 32099996-3 2020 Moreover, the treatment of these cells with bis-indole derived NR4A1 ligands 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) and its buttressed 3-chloro-5-methoxy analog (DIM-C-pPhOH-3-Cl-5-OCH3) inhibited cell growth and induced apoptosis and related genes. 3-chloro-5-methoxy 157-175 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 32099996-0 2020 BIS-INDOLE DERIVED NUCLEAR RECEPTOR 4A1 (NR4A1, Nur77) LIGANDS AS INHIBITORS OF ENDOMETRIOSIS. bis-indole 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 32099996-3 2020 Moreover, the treatment of these cells with bis-indole derived NR4A1 ligands 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) and its buttressed 3-chloro-5-methoxy analog (DIM-C-pPhOH-3-Cl-5-OCH3) inhibited cell growth and induced apoptosis and related genes. bis-indole 44-54 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 32099996-3 2020 Moreover, the treatment of these cells with bis-indole derived NR4A1 ligands 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) and its buttressed 3-chloro-5-methoxy analog (DIM-C-pPhOH-3-Cl-5-OCH3) inhibited cell growth and induced apoptosis and related genes. dim-c-pphoh-3-cl-5-och3 184-207 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 32099996-7 2020 Thus, bis-indole derived NR4A1 ligands represent a novel class of drugs as non-hormonal therapy for endometriosis. bis-indole 6-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-30 32031889-0 2020 MK-2206 and Standard Neoadjuvant Chemotherapy Improves Response in Patients With Human Epidermal Growth Factor Receptor 2-Positive and/or Hormone Receptor-Negative Breast Cancers in the I-SPY 2 Trial. MK 2206 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 138-154 32031889-10 2020 RESULTS: MK-2206 graduated with 94 patients and 57 concurrently randomly assigned controls in 3 graduation signatures: HR-negative/HER2-positive, HR-negative, and HER2-positive. MK 2206 9-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-121 32031889-14 2020 CONCLUSION: The Akt inhibitor MK-2206 combined with standard neoadjuvant therapy resulted in higher estimated pCR rates in HR-negative and HER2-positive breast cancer. MK 2206 30-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-125 30941738-10 2020 In conclusion, we confirmed a significant relationship between kinetic parameters measured by dynamic PET and the routinely assessed clinicopathological factors of breast cancer: high-grade, hormone-receptor negative tumors with high proliferation rate are characterized by higher cellular FDG-uptake and FDG-phosphorylation rate. Fluorodeoxyglucose F18 290-293 nuclear receptor subfamily 4 group A member 1 Homo sapiens 191-207 32864625-1 2020 Alpelisib is a selective inhibitor of PI3Kalpha, shown to improve outcomes for PIK3CA mutant, hormone receptor positive (HR+) metastatic breast cancers (MBC) when combined with antiestrogen therapy. Alpelisib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-110 32183020-4 2020 In breast cancer (BC), dual CDK4/6 inhibitors, palbociclib, ribociclib, and abemaciclib, combined with other agents, were approved by the Food and Drug Administration (FDA) recently for the treatment of hormone receptor positive (HR+) advanced or metastatic breast cancer (A/MBC), as well as other sub-types of breast cancer. palbociclib 47-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 203-219 32230859-7 2020 Our results suggest that hyperglycemia leads to: 1) A reduction in PI3P and PIP3, with increased PI4P that is later converted to PI(3,4)P2 at the cell surface in hormone receptor positive breast cancer; 2) a reduction in PI3P and PI4P with increased PIP3 surface expression in human epidermal growth factor receptor 2-positive (HER2+) breast cancer; and 3) an increase in di- and tri-phosphorylated PIs due to turnover of PI3P in triple negative breast cancer. phosphoinositide-3,4-bisphosphate 129-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 162-178 32230859-7 2020 Our results suggest that hyperglycemia leads to: 1) A reduction in PI3P and PIP3, with increased PI4P that is later converted to PI(3,4)P2 at the cell surface in hormone receptor positive breast cancer; 2) a reduction in PI3P and PI4P with increased PIP3 surface expression in human epidermal growth factor receptor 2-positive (HER2+) breast cancer; and 3) an increase in di- and tri-phosphorylated PIs due to turnover of PI3P in triple negative breast cancer. Phosphatidylinositols 399-402 nuclear receptor subfamily 4 group A member 1 Homo sapiens 162-178 32258036-8 2020 The phosphorylation of NR4A1 was increased in human osteoarthritis cartilage, and p38 inhibitor SB203580, JNK inhibitor SP600125 and ERK inhibitor FR180204 could significantly inhibited IL-1beta induced NR4A1 phosphorylation. SB 203580 96-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-28 32258036-8 2020 The phosphorylation of NR4A1 was increased in human osteoarthritis cartilage, and p38 inhibitor SB203580, JNK inhibitor SP600125 and ERK inhibitor FR180204 could significantly inhibited IL-1beta induced NR4A1 phosphorylation. pyrazolanthrone 120-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-28 32258036-8 2020 The phosphorylation of NR4A1 was increased in human osteoarthritis cartilage, and p38 inhibitor SB203580, JNK inhibitor SP600125 and ERK inhibitor FR180204 could significantly inhibited IL-1beta induced NR4A1 phosphorylation. FR 180204 147-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-28 32258036-8 2020 The phosphorylation of NR4A1 was increased in human osteoarthritis cartilage, and p38 inhibitor SB203580, JNK inhibitor SP600125 and ERK inhibitor FR180204 could significantly inhibited IL-1beta induced NR4A1 phosphorylation. FR 180204 147-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 203-208 32258036-9 2020 Reactivation of NR4A1 by its agonist cytosporone B could inhibit IL-1beta induced chondrocyte inflammation and expression of COX-2, iNOS, MMP3, MMP9, and MMP13. cytosporone B 37-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 16-21 32440468-3 2020 Herein, a new form of stable all-nitrogen molecular crystals consisting of only bispentazole N10 molecules with exceedingly high energy density is predicted. Nitrogen 33-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-96 32440468-3 2020 Herein, a new form of stable all-nitrogen molecular crystals consisting of only bispentazole N10 molecules with exceedingly high energy density is predicted. bispentazole 80-92 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-96 31930333-5 2020 Interestingly, we found that a small molecule inhibitor of the arginine methyltransferases CARM1 and PRMT6 was able to increase, in a gene specific manner, the number of active alleles/cell before and after hormonal stimulation, suggesting that mechanisms do indeed exist to modulate hormone receptor responses at the single cell and allele level. Arginine Vasopressin 63-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 284-300 31959898-4 2020 Here, we demonstrate that Nur77 could inhibit HCC development via transcriptional activation of the lncRNA WAP four-disulfide core domain 21 pseudogene (WFDC21P). Disulfides 116-125 nuclear receptor subfamily 4 group A member 1 Homo sapiens 26-31 31959898-9 2020 Cytosporone-B (Csn-B), an agonist for Nur77, could stimulate WFDC21P expression and suppress HCC in a WFDC21P-dependent manner. cytosporone B 0-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 31959898-9 2020 Cytosporone-B (Csn-B), an agonist for Nur77, could stimulate WFDC21P expression and suppress HCC in a WFDC21P-dependent manner. cytosporone B 15-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 31746366-3 2020 The results demonstrated that NR4A1 was significantly upregulated in TNF-alpha and CHX exposed chondrocytes. Cycloheximide 83-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-35 31574241-8 2020 Nur77 and 6-MP may provide a basis to develop a new treatment for patients who suffer from embryo adhesion dysfunction.Abbreviations: HB-EGF: heparin-binding epidermal growth factor-like growth factor; HOXA10: homeobox A10; NGFI-B: nerve growth factor-induced gene B; RIF: recurrent implantation failure; RPL: recurrent pregnancy loss; 6-MP: 6-mercaptopurine; IGFBP-1: insulin-like growth factor binding protein-1; LIF: leukemia inhibitory factor; IL-1beta: Interleukin - 1beta; CRISPR/Cas9: Clustered Regularly Interspaced Short Palindromic Repeats; AF-1: activation function-1 domain; HIF-1alpha: hypoxia-inducible factor 1alpha; CREB: cAMP response element binding. Heparin 142-149 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 31574241-8 2020 Nur77 and 6-MP may provide a basis to develop a new treatment for patients who suffer from embryo adhesion dysfunction.Abbreviations: HB-EGF: heparin-binding epidermal growth factor-like growth factor; HOXA10: homeobox A10; NGFI-B: nerve growth factor-induced gene B; RIF: recurrent implantation failure; RPL: recurrent pregnancy loss; 6-MP: 6-mercaptopurine; IGFBP-1: insulin-like growth factor binding protein-1; LIF: leukemia inhibitory factor; IL-1beta: Interleukin - 1beta; CRISPR/Cas9: Clustered Regularly Interspaced Short Palindromic Repeats; AF-1: activation function-1 domain; HIF-1alpha: hypoxia-inducible factor 1alpha; CREB: cAMP response element binding. Heparin 142-149 nuclear receptor subfamily 4 group A member 1 Homo sapiens 224-230 31706684-5 2020 These s-triazine compounds were generally more selective towards hormone receptor-positive breast cancer cell line MCF-7 than the triple negative MDA-MB-231 cell line. Triazines 6-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 65-81 31746366-2 2020 The present study aimed to investigate the role of NR4A1 in regulating chondrocyte death in response to tumor necrosis factor-alpha (TNF-alpha) and cycloheximide (CHX) treatment, with a focus on mitochondrial fission and the AMP-activated protein kinase (AMPK) signaling pathway. Cycloheximide 148-161 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-56 31746366-2 2020 The present study aimed to investigate the role of NR4A1 in regulating chondrocyte death in response to tumor necrosis factor-alpha (TNF-alpha) and cycloheximide (CHX) treatment, with a focus on mitochondrial fission and the AMP-activated protein kinase (AMPK) signaling pathway. Cycloheximide 163-166 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-56 31669267-4 2020 RESULTS: The assessment of HR status showed that the overall positive estrogen receptor (ER) and progesterone receptor (PR) rates were 71.7% and 63.7% (range, 60.9%-87.9% and 43.9%-84.8%), respectively. Estrogens 70-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-29 32060053-0 2020 Phase II study of pembrolizumab and capecitabine for triple negative and hormone receptor-positive, HER2-negative endocrine-refractory metastatic breast cancer. Capecitabine 36-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 73-89 31746366-2 2020 The present study aimed to investigate the role of NR4A1 in regulating chondrocyte death in response to tumor necrosis factor-alpha (TNF-alpha) and cycloheximide (CHX) treatment, with a focus on mitochondrial fission and the AMP-activated protein kinase (AMPK) signaling pathway. Adenosine Monophosphate 225-228 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-56 31746366-6 2020 Inhibiting NR4A1 attenuated TNF-alpha and CHX-induced mitochondrial fission and, thus, reduced mitochondrial dysfunction in chondrocytes, mPTP opening-related cell death and migration injury. Cycloheximide 42-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-16 31828441-4 2019 Alpelisib in combination with fulvestrant is now available in the clinic for postmenopausal women with advanced or metastatic hormone receptor (HR)-positive, HER2-negative, PIK3CA-mutated breast cancer. Alpelisib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-148 31563959-1 2020 Importance: Statistically significant overall survival (OS) benefits of CDK4 and CDK6 inhibitors in combination with fulvestrant for hormone receptor (HR)-positive, ERBB2 (formerly HER2)-negative advanced breast cancer (ABC) in patients regardless of menopausal status after prior endocrine therapy (ET) has not yet been demonstrated. ici 182,780 117-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-149 31769341-6 2020 Conclusion: CYP2D6*10 pharmacogenetic-guided selective estrogen receptor modulator can be a cost-effective strategy in the Chinese patients with hormone receptor-positive breast cancer. Estrogens 55-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-161 31794572-11 2019 Also, L-octanoylcarnitine levels differed according to tumor size and hormone receptor expression. octanoylcarnitine 6-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-86 31859349-5 2019 A recent large randomized trial in patients with endocrine-resistant PIK3CA-mutant hormone receptor (HR)-positive tumors led to the approval of the first PI3K inhibitor, alpelisib, in combination with fulvestrant. Alpelisib 170-179 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-99 31859349-5 2019 A recent large randomized trial in patients with endocrine-resistant PIK3CA-mutant hormone receptor (HR)-positive tumors led to the approval of the first PI3K inhibitor, alpelisib, in combination with fulvestrant. Alpelisib 170-179 nuclear receptor subfamily 4 group A member 1 Homo sapiens 101-103 31727981-1 2019 We previously reported the identification of a novel antimitotic agent with carbazole and benzohydrazide structures: N"-[(9-ethyl-9H-carbazol-3-yl)methylene]-2-iodobenzohydrazide (code number NP-10). carbazole 76-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 192-197 31025302-0 2019 Cost-Effectiveness Analysis of Fulvestrant 500 mg in Endocrine Therapy-Naive Postmenopausal Women with Hormone Receptor-Positive Advanced Breast Cancer in the UK. Fulvestrant 31-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-119 31771627-11 2019 Our organoid model system revealed important insights into the role of PR in BRCA1-mutated benign breast cells and the critical paracrine actions that modify hormone receptor (HR)-negative cells. organoid 4-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 158-174 31771627-11 2019 Our organoid model system revealed important insights into the role of PR in BRCA1-mutated benign breast cells and the critical paracrine actions that modify hormone receptor (HR)-negative cells. organoid 4-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 176-178 31727981-1 2019 We previously reported the identification of a novel antimitotic agent with carbazole and benzohydrazide structures: N"-[(9-ethyl-9H-carbazol-3-yl)methylene]-2-iodobenzohydrazide (code number NP-10). benzoylhydrazine 90-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 192-197 31727981-1 2019 We previously reported the identification of a novel antimitotic agent with carbazole and benzohydrazide structures: N"-[(9-ethyl-9H-carbazol-3-yl)methylene]-2-iodobenzohydrazide (code number NP-10). n"-[(9-ethyl-9h-carbazol-3-yl)methylene]-2-iodobenzohydrazide 117-178 nuclear receptor subfamily 4 group A member 1 Homo sapiens 192-197 31839811-0 2019 Fenretinide-induced Apoptosis of Acute Myeloid Leukemia Cells via NR4A1 Translocation into Mitochondria and Bcl-2 Transformation. Fenretinide 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-71 31079343-2 2019 METHODS: Meta-analysis of randomized controlled trials (RCTs) evaluating fulvestrant 500 mg in postmenopausal hormone receptor-positive ABC, to evaluate differences in clinical benefit rate (CBR; proportion of patients experiencing best overall response of complete response, partial response, or stable disease for >= 24 weeks) between fulvestrant 500 mg and comparator endocrine therapies. Fulvestrant 73-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-126 31079343-10 2019 CONCLUSIONS: In postmenopausal patients with hormone receptor-positive ABC, fulvestrant 500 mg first-line was associated with significantly greater CBR (more patients benefiting from treatment) vs. comparator endocrine therapy. Fulvestrant 76-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-61 31839811-1 2019 OBJECTIVE: Fenretinide is reported to induce NR4A1-associated apoptosis in several types of cancer cells. Fenretinide 11-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-50 31839811-7 2019 In addition, the expression levels of NR4A1 in the nuclei and mitochondria of fenretinide-treated AML cells were also measured. Fenretinide 78-89 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 31839811-11 2019 Fenretinide induced the expression of NR4A1 and mitochondria-mediated apoptotic pathway-associated proteins in a time- and concentration-dependent manner. Fenretinide 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 31839811-13 2019 Under the action of fenretinide, the NR4A1 protein expression was down-regulated in nuclear extracts whereas up-regulated in mitochondrial extracts. Fenretinide 20-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-42 31839811-14 2019 At the same time, fenretinide promoted NR4A1 translocation from nuclei into mitochondria, and enhanced the interaction between NR4A1 and Bcl-2, thereby exposing the BH3 domain of Bcl-2 to exert the anti-apoptotic effect. Fenretinide 18-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 31839811-14 2019 At the same time, fenretinide promoted NR4A1 translocation from nuclei into mitochondria, and enhanced the interaction between NR4A1 and Bcl-2, thereby exposing the BH3 domain of Bcl-2 to exert the anti-apoptotic effect. Fenretinide 18-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 127-132 31839811-17 2019 Besides, the NR4A1-mediated signaling pathway is highly involved in the fenretinide-induced apoptosis of AML cells. Fenretinide 72-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 31638935-10 2019 A subgroup analysis revealed that the HER2+/HR- patients who received H + P showed the highest increase in the pCR. Phlorhizin 74-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-46 31462501-0 2019 Inhibition of NR4A1 Promotes Ros Accumulation and IL24-Dependent Growth Arrest in Rhabdomyosarcoma. Reactive Oxygen Species 29-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-19 31462501-1 2019 Nuclear receptor 4A1 (NR4A1, Nur77) is overexpressed in rhabdomyosarcoma (RMS), and inactivation of NR4A1 (siNR4A1) or treatment with the NR4A1 antagonist 1,1-bis(3"-indoly)-1-(p-hydroxy-phenyl)methane (DIM-C-pPhOH) has antiproliferative and proapoptotic effects on RMS cells. 1,1-bis(3"-indoly)-1-(p-hydroxy-phenyl)methane 155-201 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-20 31462501-1 2019 Nuclear receptor 4A1 (NR4A1, Nur77) is overexpressed in rhabdomyosarcoma (RMS), and inactivation of NR4A1 (siNR4A1) or treatment with the NR4A1 antagonist 1,1-bis(3"-indoly)-1-(p-hydroxy-phenyl)methane (DIM-C-pPhOH) has antiproliferative and proapoptotic effects on RMS cells. 1,1-bis(3"-indoly)-1-(p-hydroxy-phenyl)methane 155-201 nuclear receptor subfamily 4 group A member 1 Homo sapiens 22-27 31462501-1 2019 Nuclear receptor 4A1 (NR4A1, Nur77) is overexpressed in rhabdomyosarcoma (RMS), and inactivation of NR4A1 (siNR4A1) or treatment with the NR4A1 antagonist 1,1-bis(3"-indoly)-1-(p-hydroxy-phenyl)methane (DIM-C-pPhOH) has antiproliferative and proapoptotic effects on RMS cells. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 203-214 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-20 31462501-1 2019 Nuclear receptor 4A1 (NR4A1, Nur77) is overexpressed in rhabdomyosarcoma (RMS), and inactivation of NR4A1 (siNR4A1) or treatment with the NR4A1 antagonist 1,1-bis(3"-indoly)-1-(p-hydroxy-phenyl)methane (DIM-C-pPhOH) has antiproliferative and proapoptotic effects on RMS cells. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 203-214 nuclear receptor subfamily 4 group A member 1 Homo sapiens 22-27 31462501-3 2019 Here, we report that NR4A1 silencing or inhibition resulted in accumulation of reactive oxygen species (ROS) and ROS-dependent induction of the tumor suppressor-like cytokine IL24 in RMS cells. Reactive Oxygen Species 79-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 21-26 31462501-3 2019 Here, we report that NR4A1 silencing or inhibition resulted in accumulation of reactive oxygen species (ROS) and ROS-dependent induction of the tumor suppressor-like cytokine IL24 in RMS cells. Reactive Oxygen Species 104-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 21-26 31462501-3 2019 Here, we report that NR4A1 silencing or inhibition resulted in accumulation of reactive oxygen species (ROS) and ROS-dependent induction of the tumor suppressor-like cytokine IL24 in RMS cells. Reactive Oxygen Species 113-116 nuclear receptor subfamily 4 group A member 1 Homo sapiens 21-26 31462501-5 2019 Silencing TXNDC5 and IDH1 also induced ROS accumulation and IL24 expression in RMS cells, suggesting that NR4A1 antagonists mediate their antiproliferative and apoptotic effects through modulation of proreductant gene expression. Reactive Oxygen Species 39-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-111 31462501-6 2019 Finally, cotreatment with the antioxidant glutathione or IL24-blocking antibody reversed the effects of NR4A1 inhibition, demonstrating the importance of both ROS and IL24 in mediating the cellular responses.Implications: Overall, these data elucidate the mechanism by which NR4A1 inhibition functions to inhibit the proliferation, survival, and migration of RMS cells. Glutathione 42-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-109 31462501-6 2019 Finally, cotreatment with the antioxidant glutathione or IL24-blocking antibody reversed the effects of NR4A1 inhibition, demonstrating the importance of both ROS and IL24 in mediating the cellular responses.Implications: Overall, these data elucidate the mechanism by which NR4A1 inhibition functions to inhibit the proliferation, survival, and migration of RMS cells. Glutathione 42-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 275-280 31462501-6 2019 Finally, cotreatment with the antioxidant glutathione or IL24-blocking antibody reversed the effects of NR4A1 inhibition, demonstrating the importance of both ROS and IL24 in mediating the cellular responses.Implications: Overall, these data elucidate the mechanism by which NR4A1 inhibition functions to inhibit the proliferation, survival, and migration of RMS cells. Reactive Oxygen Species 159-162 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-109 31486299-5 2019 Fluoride release (N = 10) was evaluated in CG, SG and UG after cariogenic challenge for 11 days. Fluorides 0-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-24 31486299-5 2019 Fluoride release (N = 10) was evaluated in CG, SG and UG after cariogenic challenge for 11 days. cysteinylglycine 43-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-24 31498970-2 2019 With increasing the oligofluorene arm length, absorption spectra were red-shifted progressively, whereas an increase in photoluminescence quantum yields (PLQYs) and optical gain coefficients, and a corresponding reduction in amplified spontaneous emission (ASE) thresholds and loss coefficients were observed for Tr1-Tr3 except for Tr4. oligofluorene 20-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 317-320 31788435-3 2019 Research showed the potential of depsidones as a treatment option for hormone receptor-positive breast cancer treatment, yet its effects on hormone receptor-negative breast cancer are still unkown. depsidone 33-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-86 31492735-0 2019 Molecular, Chemical, and Structural Characterization of Prostaglandin A2 as a Novel Agonist for Nur77. prostaglandin A2 56-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-101 31492735-4 2019 However, several more recent studies indicate that small synthetic molecules and unsaturated fatty acids can bind to Nur77. Fatty Acids, Unsaturated 81-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 117-122 31492735-8 2019 Our data show that PGA2 induces Nur77 transcriptional activity by forming a covalent adduct between its endocyclic beta-carbon, C9, and Cys566 in the receptor"s ligand-binding domain. prostaglandin A2 19-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-37 31492735-8 2019 Our data show that PGA2 induces Nur77 transcriptional activity by forming a covalent adduct between its endocyclic beta-carbon, C9, and Cys566 in the receptor"s ligand-binding domain. beta-carbon 115-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-37 31492735-9 2019 The importance of this endocyclic beta-carbon was substantiated by the failure of prostaglandins without such electrophilic properties to react with Nur77. Prostaglandins 82-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-154 31492735-10 2019 Calculated chemical properties and data from reactive molecular dynamic simulations, intrinsic reaction coordinate modeling, and covalent molecular docking also corroborate the selectivity of PGA2"s C9 beta-carbon towards Nur77"s Cys. prostaglandin A2 192-196 nuclear receptor subfamily 4 group A member 1 Homo sapiens 222-227 31492735-10 2019 Calculated chemical properties and data from reactive molecular dynamic simulations, intrinsic reaction coordinate modeling, and covalent molecular docking also corroborate the selectivity of PGA2"s C9 beta-carbon towards Nur77"s Cys. beta-carbon 202-213 nuclear receptor subfamily 4 group A member 1 Homo sapiens 222-227 31492735-10 2019 Calculated chemical properties and data from reactive molecular dynamic simulations, intrinsic reaction coordinate modeling, and covalent molecular docking also corroborate the selectivity of PGA2"s C9 beta-carbon towards Nur77"s Cys. Cysteine 230-233 nuclear receptor subfamily 4 group A member 1 Homo sapiens 222-227 31492735-11 2019 In summary, our molecular, chemical, and structural characterization of the PGA2-Nur77 interaction provides the first evidence that PGA2 is an endogenous Nur77 agonist. prostaglandin A2 76-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-86 31492735-11 2019 In summary, our molecular, chemical, and structural characterization of the PGA2-Nur77 interaction provides the first evidence that PGA2 is an endogenous Nur77 agonist. prostaglandin A2 76-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-159 31492735-11 2019 In summary, our molecular, chemical, and structural characterization of the PGA2-Nur77 interaction provides the first evidence that PGA2 is an endogenous Nur77 agonist. prostaglandin A2 132-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-86 31492735-11 2019 In summary, our molecular, chemical, and structural characterization of the PGA2-Nur77 interaction provides the first evidence that PGA2 is an endogenous Nur77 agonist. prostaglandin A2 132-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-159 31551757-6 2019 Peri-menopause is marked by widely fluctuating estrogen levels resulting in periods of irregular hormone-receptor interactions. Estrogens 47-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-113 31533777-1 2019 BACKGROUND: The biological effect of oral metronomic vinorelbine (mVNB) alone or in combination with endocrine therapy in patients with hormone receptor-positive (HR+)/HER2-negative breast cancer has been scarcely addressed. Vinorelbine 53-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 136-152 31533777-1 2019 BACKGROUND: The biological effect of oral metronomic vinorelbine (mVNB) alone or in combination with endocrine therapy in patients with hormone receptor-positive (HR+)/HER2-negative breast cancer has been scarcely addressed. mvnb 66-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 136-152 31339827-12 2019 With longer follow-up, standard chemotherapy remains superior to capecitabine among hormone receptor-negative patients (HR, 0.66; P = .02), but not among hormone receptor-positive patients (HR, 0.89; P = .43). Capecitabine 65-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-100 31339827-15 2019 CONCLUSION: With longer follow-up, RFS remains superior for standard adjuvant chemotherapy versus capecitabine, especially in patients with hormone receptor-negative disease. Capecitabine 98-110 nuclear receptor subfamily 4 group A member 1 Homo sapiens 140-156 31273046-0 2019 Prevention of progression of pulmonary hypertension by the Nur77 agonist 6-mercaptopurine: role of BMP signalling. Mercaptopurine 73-89 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-64 31273046-3 2019 Orphan nuclear receptor Nur77 is a key regulator of proliferation and inflammation in vascular cells, but its role in impaired BMP signalling and vascular remodelling in PAH is unknown.We hypothesised that activation of Nur77 by 6-mercaptopurine (6-MP) would improve PAH by inhibiting endothelial cell dysfunction and vascular remodelling.Nur77 expression is decreased in cultured pulmonary microvascular endothelial cells (MVECs) and lungs of PAH patients. Mercaptopurine 229-245 nuclear receptor subfamily 4 group A member 1 Homo sapiens 24-29 31273046-3 2019 Orphan nuclear receptor Nur77 is a key regulator of proliferation and inflammation in vascular cells, but its role in impaired BMP signalling and vascular remodelling in PAH is unknown.We hypothesised that activation of Nur77 by 6-mercaptopurine (6-MP) would improve PAH by inhibiting endothelial cell dysfunction and vascular remodelling.Nur77 expression is decreased in cultured pulmonary microvascular endothelial cells (MVECs) and lungs of PAH patients. Mercaptopurine 229-245 nuclear receptor subfamily 4 group A member 1 Homo sapiens 220-225 31273046-3 2019 Orphan nuclear receptor Nur77 is a key regulator of proliferation and inflammation in vascular cells, but its role in impaired BMP signalling and vascular remodelling in PAH is unknown.We hypothesised that activation of Nur77 by 6-mercaptopurine (6-MP) would improve PAH by inhibiting endothelial cell dysfunction and vascular remodelling.Nur77 expression is decreased in cultured pulmonary microvascular endothelial cells (MVECs) and lungs of PAH patients. Mercaptopurine 229-245 nuclear receptor subfamily 4 group A member 1 Homo sapiens 220-225 31273046-3 2019 Orphan nuclear receptor Nur77 is a key regulator of proliferation and inflammation in vascular cells, but its role in impaired BMP signalling and vascular remodelling in PAH is unknown.We hypothesised that activation of Nur77 by 6-mercaptopurine (6-MP) would improve PAH by inhibiting endothelial cell dysfunction and vascular remodelling.Nur77 expression is decreased in cultured pulmonary microvascular endothelial cells (MVECs) and lungs of PAH patients. Mercaptopurine 247-251 nuclear receptor subfamily 4 group A member 1 Homo sapiens 220-225 31273046-3 2019 Orphan nuclear receptor Nur77 is a key regulator of proliferation and inflammation in vascular cells, but its role in impaired BMP signalling and vascular remodelling in PAH is unknown.We hypothesised that activation of Nur77 by 6-mercaptopurine (6-MP) would improve PAH by inhibiting endothelial cell dysfunction and vascular remodelling.Nur77 expression is decreased in cultured pulmonary microvascular endothelial cells (MVECs) and lungs of PAH patients. Mercaptopurine 247-251 nuclear receptor subfamily 4 group A member 1 Homo sapiens 220-225 31127979-0 2019 N10 -carbonyl-substituted phenothiazines inhibiting lipid peroxidation and associated nitric oxide consumption powerfully protect brain tissue against oxidative stress. Nitric Oxide 86-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-3 31153828-1 2019 Tamoxifen is the most commonly used endocrine therapy for patients with hormone receptor (HR)-positive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-88 31153828-1 2019 Tamoxifen is the most commonly used endocrine therapy for patients with hormone receptor (HR)-positive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-92 31119568-0 2019 Potent inhibition of breast cancer by bis-indole-derived nuclear receptor 4A1 (NR4A1) antagonists. bis-indole 38-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-77 31132532-0 2019 SAR study of celastrol analogs targeting Nur77-mediated inflammatory pathway. celastrol 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 31132532-2 2019 Our previous work found that celastrol, a pentacyclic triterpene, bound to Nur77 to inhibit inflammation in a Nur77-dependent manner. celastrol 29-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-80 31132532-2 2019 Our previous work found that celastrol, a pentacyclic triterpene, bound to Nur77 to inhibit inflammation in a Nur77-dependent manner. celastrol 29-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-115 31132532-2 2019 Our previous work found that celastrol, a pentacyclic triterpene, bound to Nur77 to inhibit inflammation in a Nur77-dependent manner. Triterpenes 54-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-80 31132532-2 2019 Our previous work found that celastrol, a pentacyclic triterpene, bound to Nur77 to inhibit inflammation in a Nur77-dependent manner. Triterpenes 54-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-115 31132532-3 2019 Celastrol binding to Nur77 promotes Nur77 translocation from nucleus to cytoplasm, resulting in clearance of inflamed mitochondria and then alleviation of inflammation. celastrol 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 21-26 31132532-3 2019 Celastrol binding to Nur77 promotes Nur77 translocation from nucleus to cytoplasm, resulting in clearance of inflamed mitochondria and then alleviation of inflammation. celastrol 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 36-41 31312859-5 2019 Western blotting data further confirmed that NUR77 was highly expressed in primary human term placental STB and the FSK-induced BeWo cell line. fsk 116-119 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-50 31298848-3 2019 On a longer (hundreds of ns) timescale, this species rearranges to a ring-opened diazo compound, which we have also detected by time-resolved infrared and TR3 spectroscopy. diazo compound 81-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 155-158 31051411-1 2019 BACKGROUND: Endocrine treatment with Tamoxifen and aromatase inhibitors (AIs) is a staple in the management of hormone receptor positive breast cancer (HR + BC). Tamoxifen 37-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-127 31119568-0 2019 Potent inhibition of breast cancer by bis-indole-derived nuclear receptor 4A1 (NR4A1) antagonists. bis-indole 38-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-84 31119568-1 2019 BACKGROUND: Nuclear receptor 4A1 (NR4A1) is overexpressed in mammary tumors, and the methylene-substituted bis-indole derivative 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) acts as an NR4A1 antagonist (inverse agonist) and inhibits NR4A1-regulated pro-oncogenic pathways/genes in breast and other cancer cells. methylene-substituted bis-indole 85-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-39 31119568-1 2019 BACKGROUND: Nuclear receptor 4A1 (NR4A1) is overexpressed in mammary tumors, and the methylene-substituted bis-indole derivative 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) acts as an NR4A1 antagonist (inverse agonist) and inhibits NR4A1-regulated pro-oncogenic pathways/genes in breast and other cancer cells. methylene-substituted bis-indole 85-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 201-206 31119568-1 2019 BACKGROUND: Nuclear receptor 4A1 (NR4A1) is overexpressed in mammary tumors, and the methylene-substituted bis-indole derivative 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) acts as an NR4A1 antagonist (inverse agonist) and inhibits NR4A1-regulated pro-oncogenic pathways/genes in breast and other cancer cells. methylene-substituted bis-indole 85-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 201-206 31119568-1 2019 BACKGROUND: Nuclear receptor 4A1 (NR4A1) is overexpressed in mammary tumors, and the methylene-substituted bis-indole derivative 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) acts as an NR4A1 antagonist (inverse agonist) and inhibits NR4A1-regulated pro-oncogenic pathways/genes in breast and other cancer cells. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 129-175 nuclear receptor subfamily 4 group A member 1 Homo sapiens 201-206 31119568-1 2019 BACKGROUND: Nuclear receptor 4A1 (NR4A1) is overexpressed in mammary tumors, and the methylene-substituted bis-indole derivative 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) acts as an NR4A1 antagonist (inverse agonist) and inhibits NR4A1-regulated pro-oncogenic pathways/genes in breast and other cancer cells. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 129-175 nuclear receptor subfamily 4 group A member 1 Homo sapiens 201-206 31119568-1 2019 BACKGROUND: Nuclear receptor 4A1 (NR4A1) is overexpressed in mammary tumors, and the methylene-substituted bis-indole derivative 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) acts as an NR4A1 antagonist (inverse agonist) and inhibits NR4A1-regulated pro-oncogenic pathways/genes in breast and other cancer cells. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 177-188 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-32 31119568-1 2019 BACKGROUND: Nuclear receptor 4A1 (NR4A1) is overexpressed in mammary tumors, and the methylene-substituted bis-indole derivative 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) acts as an NR4A1 antagonist (inverse agonist) and inhibits NR4A1-regulated pro-oncogenic pathways/genes in breast and other cancer cells. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 177-188 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-39 31119568-7 2019 DIM-C-pPhOH is rapidly metabolized and the effects and potencies of buttressed analogs of DIM-C-pPhOH which contain one or two substituents ortho to the hydroxyl groups were investigated using NR4A1-regulated gene/gene products as endpoints. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 193-198 31053403-0 2019 Nuclear receptor 4A1 (NR4A1) antagonists induce ROS-dependent inhibition of mTOR signaling in endometrial cancer. ros 48-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-20 31146160-1 2019 Tamoxifen (TAM) is a first generation-SERM administered for hormone receptor-positive (HER+) breast cancer in both pre- and post-menopausal patients and may undergo metabolic activation in organisms that share similar receptors and thus face comparable mechanisms of response. Tamoxifen 11-14 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-77 30980508-0 2019 Synergistic effects of hormone therapy drugs and usnic acid on hormone receptor-positive breast and prostate cancer cells. usnic acid 49-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-79 30980508-1 2019 The aim of this study was to investigate the combined effects of usnic acid (UA) and Tamoxifen (Tam) or Enzalutamide (Enz) on hormone receptor-positive breast and prostate cancer (BC and PC), respectively. usnic acid 65-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 30980508-1 2019 The aim of this study was to investigate the combined effects of usnic acid (UA) and Tamoxifen (Tam) or Enzalutamide (Enz) on hormone receptor-positive breast and prostate cancer (BC and PC), respectively. usnic acid 77-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 30980508-1 2019 The aim of this study was to investigate the combined effects of usnic acid (UA) and Tamoxifen (Tam) or Enzalutamide (Enz) on hormone receptor-positive breast and prostate cancer (BC and PC), respectively. Tamoxifen 85-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 30980508-1 2019 The aim of this study was to investigate the combined effects of usnic acid (UA) and Tamoxifen (Tam) or Enzalutamide (Enz) on hormone receptor-positive breast and prostate cancer (BC and PC), respectively. Tamoxifen 85-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 30980508-1 2019 The aim of this study was to investigate the combined effects of usnic acid (UA) and Tamoxifen (Tam) or Enzalutamide (Enz) on hormone receptor-positive breast and prostate cancer (BC and PC), respectively. enzalutamide 104-116 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 30980508-1 2019 The aim of this study was to investigate the combined effects of usnic acid (UA) and Tamoxifen (Tam) or Enzalutamide (Enz) on hormone receptor-positive breast and prostate cancer (BC and PC), respectively. enzalutamide 104-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 31413807-0 2019 Synthesis of Highly Potent N-10 Amino-Linked DNA-Alkylating Indolinobenzodiazepine Antibody-Drug Conjugates (ADCs). indolinobenzodiazepine 60-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-31 31413807-3 2019 Here, we present an alternative strategy for the IGNs, linking through a carbamate at the readily available N-10 amine present in the monoimine containing dimer. Carbamates 73-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-112 31413807-3 2019 Here, we present an alternative strategy for the IGNs, linking through a carbamate at the readily available N-10 amine present in the monoimine containing dimer. monoimine 134-143 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-112 31331091-0 2019 Autoantibodies Specific to ERalpha are Involved in Tamoxifen Resistance in Hormone Receptor Positive Breast Cancer. Tamoxifen 51-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 30895534-12 2019 CONCLUSIONS: Among patients with HR-positive advanced breast cancer, the estimated PFS in patients treated with fulvestrant and palbociclib was comparable to a previously reported phase 3 trial. Fulvestrant 112-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-35 30895534-12 2019 CONCLUSIONS: Among patients with HR-positive advanced breast cancer, the estimated PFS in patients treated with fulvestrant and palbociclib was comparable to a previously reported phase 3 trial. palbociclib 128-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-35 31146160-1 2019 Tamoxifen (TAM) is a first generation-SERM administered for hormone receptor-positive (HER+) breast cancer in both pre- and post-menopausal patients and may undergo metabolic activation in organisms that share similar receptors and thus face comparable mechanisms of response. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-77 31340867-1 2019 BACKGROUND: Tamoxifen resistance remains a clinical challenge for hormone receptor-positive breast cancer. Tamoxifen 12-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-82 31337401-10 2019 We observed a lower plasmatic tryptophan and a higher kynurenine/tryptophan ratio in hormone receptor-negative patients compared to hormone receptor-positive cancers. Tryptophan 30-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 31337401-10 2019 We observed a lower plasmatic tryptophan and a higher kynurenine/tryptophan ratio in hormone receptor-negative patients compared to hormone receptor-positive cancers. Kynurenine 54-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 31337401-10 2019 We observed a lower plasmatic tryptophan and a higher kynurenine/tryptophan ratio in hormone receptor-negative patients compared to hormone receptor-positive cancers. Tryptophan 65-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 31337401-16 2019 The Kyn/Trp ratio and Trp also showed different values according to hormone receptor status, TNM stage, T grade and histology. Kynurenine 4-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-84 31337401-16 2019 The Kyn/Trp ratio and Trp also showed different values according to hormone receptor status, TNM stage, T grade and histology. Tryptophan 8-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-84 31337401-16 2019 The Kyn/Trp ratio and Trp also showed different values according to hormone receptor status, TNM stage, T grade and histology. Tryptophan 22-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-84 31053403-0 2019 Nuclear receptor 4A1 (NR4A1) antagonists induce ROS-dependent inhibition of mTOR signaling in endometrial cancer. ros 48-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 22-27 31053403-6 2019 CONCLUSIONS: NR4A1 exhibited pro-oncogenic activity in endometrial cells due, in part, to regulation of cell growth, survival and mTOR signaling, and all of these pathways and their associated gene products were inhibited after treatment with bis-indole-derived NR4A1 antagonists. bis-indole 243-253 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 31053403-6 2019 CONCLUSIONS: NR4A1 exhibited pro-oncogenic activity in endometrial cells due, in part, to regulation of cell growth, survival and mTOR signaling, and all of these pathways and their associated gene products were inhibited after treatment with bis-indole-derived NR4A1 antagonists. bis-indole 243-253 nuclear receptor subfamily 4 group A member 1 Homo sapiens 262-267 30679318-0 2019 Everolimus plus Exemestane for Hormone Receptor-Positive Advanced Breast Cancer: A PAM50 Intrinsic Subtype Analysis of BOLERO-2. exemestane 16-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-47 31115481-4 2019 We report that CS promotes Nur77 expression and nuclear export in vivo and in vitro, which increases cigarette smoke extract (CSE)-induced autophagy. Cesium 15-17 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-32 31115481-5 2019 In addition, we found that lung tissues, human bronchial epithelial (HBE) cells and A549 cells exposed to CS or CSE expressed lower levels of LC3 and Beclin-1 and contained fewer autophagosomes following Nur77 knockdown with siRNA-Nur77. Cesium 106-108 nuclear receptor subfamily 4 group A member 1 Homo sapiens 204-209 31115481-5 2019 In addition, we found that lung tissues, human bronchial epithelial (HBE) cells and A549 cells exposed to CS or CSE expressed lower levels of LC3 and Beclin-1 and contained fewer autophagosomes following Nur77 knockdown with siRNA-Nur77. Cesium 106-108 nuclear receptor subfamily 4 group A member 1 Homo sapiens 231-236 31115481-8 2019 This study illustrates the role of Nur77 in bronchial and alveolar destruction following exposure to CS. Cesium 101-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-40 30679318-0 2019 Everolimus plus Exemestane for Hormone Receptor-Positive Advanced Breast Cancer: A PAM50 Intrinsic Subtype Analysis of BOLERO-2. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-47 30981499-9 2019 Meanwhile, in quiescent satellite cells, Nr4a1 expressed is not detected, while its protein level is highly induced in both BaCl2-induced muscle regeneration followed with satellite cells activation and satellite cells of cultured single myofiber. barium chloride 124-129 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 32851295-12 2019 Vancomycin minimal inhibitory concentration (MIC) creep was found in the study period in all MRSA and ST59-SCC mec IV isolates. Vancomycin 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-106 31289516-6 2019 Hormone receptor (HR)-negative BC is associated with a higher TMB and immune gene expression compared with HR-positive BC [TMB, estrogen receptor (ER)-negative vs. ER-negative, 55 vs. 32, respectively; P=4.1x10-13; progesterone receptor (PR)-negative vs. PR-positive, 53 vs. 31, respectively; P<2.2x10-16]. 1,2,4,5-tetramethoxybenzene 62-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 31289516-6 2019 Hormone receptor (HR)-negative BC is associated with a higher TMB and immune gene expression compared with HR-positive BC [TMB, estrogen receptor (ER)-negative vs. ER-negative, 55 vs. 32, respectively; P=4.1x10-13; progesterone receptor (PR)-negative vs. PR-positive, 53 vs. 31, respectively; P<2.2x10-16]. 1,2,4,5-tetramethoxybenzene 62-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-20 31289516-10 2019 The findings of the present study suggest that HR-negative or HER2-positive BC exhibits elevated TMB and immunogenic activity, and immunotherapeutic options are recommended. 1,2,4,5-tetramethoxybenzene 97-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-49 30957282-9 2019 Compared with the Raman bands of AH+ (N1+H+ ), the TR3 bands of AH.2+ (N1+H+ ) are significantly down-shifted, indicating a decrease in the bond order of the pyrimidine and imidazole rings due to the resonance structure of AH.2+ (N1+H+ ). pyrimidine 158-168 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-54 30957282-9 2019 Compared with the Raman bands of AH+ (N1+H+ ), the TR3 bands of AH.2+ (N1+H+ ) are significantly down-shifted, indicating a decrease in the bond order of the pyrimidine and imidazole rings due to the resonance structure of AH.2+ (N1+H+ ). imidazole 173-182 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-54 30868391-0 2019 Prognostic effect of Ki-67 in common clinical subgroups of patients with HER2-negative, hormone receptor-positive early breast cancer. ki-67 21-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-104 30778520-0 2019 De-escalated therapy for HR+/HER2+ breast cancer patients with Ki67 response after 2 weeks letrozole: results of the PerELISA neoadjuvant study. Letrozole 91-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-27 31036468-22 2019 INTERPRETATION: Tucidinostat plus exemestane improved progression-free survival compared with placebo plus exemestane in patients with advanced, hormone receptor-positive, HER2-negative breast cancer that progressed after previous endocrine therapy. exemestane 34-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-161 31217631-9 2019 After treatment with captopril or AT 1 R-inhibitor candesartan, VEGF-expression decreased significantly in HR-positive and HR-negative cell lines. Captopril 21-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-109 31217631-9 2019 After treatment with captopril or AT 1 R-inhibitor candesartan, VEGF-expression decreased significantly in HR-positive and HR-negative cell lines. Captopril 21-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-125 31217631-9 2019 After treatment with captopril or AT 1 R-inhibitor candesartan, VEGF-expression decreased significantly in HR-positive and HR-negative cell lines. candesartan 51-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-109 31217631-9 2019 After treatment with captopril or AT 1 R-inhibitor candesartan, VEGF-expression decreased significantly in HR-positive and HR-negative cell lines. candesartan 51-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-125 30801912-4 2019 At 6 hours, dexamethasone treatment decreased levels of NR0B2, NR4A1, NR5A1, and NR5A2 messenger RNAs (mRNAs) and NR5A2 mRNA levels remained depressed at 12 hours. Dexamethasone 12-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 30801912-7 2019 In primary cultures of Leydig cells, 10 -9 and 10 -7 M dexamethasone decreased levels of NR4A1 and NR5A1 mRNAs and increased those of NFKBIA mRNA. Dexamethasone 55-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 30801912-8 2019 Our discovery that dexamethasone downregulates NR4A1, NR5A1, and NR5A2 genes, known to be important for testicular functions, may be part of the mechanism by which glucocorticoids acutely decreases testosterone. Dexamethasone 19-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-52 30801912-8 2019 Our discovery that dexamethasone downregulates NR4A1, NR5A1, and NR5A2 genes, known to be important for testicular functions, may be part of the mechanism by which glucocorticoids acutely decreases testosterone. Testosterone 198-210 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-52 31036468-0 2019 Tucidinostat plus exemestane for postmenopausal patients with advanced, hormone receptor-positive breast cancer (ACE): a randomised, double-blind, placebo-controlled, phase 3 trial. N-(2-amino-5-fluorobenzyl)-4-(N-(pyridine-3-acrylyl)aminomethyl)benzamide 0-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-88 30772912-7 2019 miR-21 effectively promoted the expression of the 8Br-cAMP plus medroxyprogesterone acetate (MPA)-induced hESC decidualization marker genes PRL and IGFBP-1 and morphological transformation through the modulation of KLF12 and NR4A1 expression; conversely, inhibition of miR-21 expression compromised hESC decidualization in vitro. Medroxyprogesterone Acetate 64-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 225-230 31036468-2 2019 In an exploratory study, the combination of tucidinostat with exemestane showed preliminary signs of encouraging anti-tumour activity in patients with advanced hormone receptor-positive breast cancer. N-(2-amino-5-fluorobenzyl)-4-(N-(pyridine-3-acrylyl)aminomethyl)benzamide 44-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-176 31036468-2 2019 In an exploratory study, the combination of tucidinostat with exemestane showed preliminary signs of encouraging anti-tumour activity in patients with advanced hormone receptor-positive breast cancer. exemestane 62-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-176 31036468-22 2019 INTERPRETATION: Tucidinostat plus exemestane improved progression-free survival compared with placebo plus exemestane in patients with advanced, hormone receptor-positive, HER2-negative breast cancer that progressed after previous endocrine therapy. N-(2-amino-5-fluorobenzyl)-4-(N-(pyridine-3-acrylyl)aminomethyl)benzamide 16-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-161 31091374-13 2019 CONCLUSIONS: Treatment with alpelisib-fulvestrant prolonged progression-free survival among patients with PIK3CA-mutated, HR-positive, HER2-negative advanced breast cancer who had received endocrine therapy previously. alpelisib-fulvestrant 28-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-124 31088410-0 2019 Everolimus in hormone receptor-positive metastatic breast cancer: PIK3CA mutation H1047R was a potential efficacy biomarker in a retrospective study. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-30 31088410-1 2019 BACKGROUND: Everolimus, an inhibitor of mammalian target of rapamycin (mTOR), has been shown to increase the efficacy of endocrine therapies in hormone receptor (HR)-positive metastatic breast cancer. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-160 31088410-1 2019 BACKGROUND: Everolimus, an inhibitor of mammalian target of rapamycin (mTOR), has been shown to increase the efficacy of endocrine therapies in hormone receptor (HR)-positive metastatic breast cancer. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 162-164 30772912-7 2019 miR-21 effectively promoted the expression of the 8Br-cAMP plus medroxyprogesterone acetate (MPA)-induced hESC decidualization marker genes PRL and IGFBP-1 and morphological transformation through the modulation of KLF12 and NR4A1 expression; conversely, inhibition of miR-21 expression compromised hESC decidualization in vitro. 8br-camp 50-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 225-230 30723140-1 2019 PURPOSE: Addition of alpelisib to fulvestrant significantly extended progression-free survival in PIK3CA-mutant, hormone receptor-positive (HR+) advanced/metastatic breast cancer in the phase III SOLAR-1 study. Alpelisib 21-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-129 30772912-7 2019 miR-21 effectively promoted the expression of the 8Br-cAMP plus medroxyprogesterone acetate (MPA)-induced hESC decidualization marker genes PRL and IGFBP-1 and morphological transformation through the modulation of KLF12 and NR4A1 expression; conversely, inhibition of miR-21 expression compromised hESC decidualization in vitro. Medroxyprogesterone Acetate 93-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 225-230 30973961-4 2019 We aimed to elucidate the regulation of NR4A1 and its significance in Hcy-induced NAFLD. Homocysteine 70-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-45 30515770-0 2019 Dietary cadmium and risk of breast cancer subtypes defined by hormone receptor status: A prospective cohort study. Cadmium 8-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-78 30973961-6 2019 Furthermore, Hcy enhanced p300 and decreased HDAC7 recruitment to the NR4A1 promoter, resulting in histone H3K27 hyperacetylation and NR4A1 upregulation. Homocysteine 13-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-75 30973961-6 2019 Furthermore, Hcy enhanced p300 and decreased HDAC7 recruitment to the NR4A1 promoter, resulting in histone H3K27 hyperacetylation and NR4A1 upregulation. Homocysteine 13-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 134-139 30973961-7 2019 Moreover, NR4A1 depletion not only mimicked but also exaggerated the effects of Hcy on steatosis, whereas NR4A1 agonist Cytosporone B (CsnB) blocked Hcy-induced steatosis. Homocysteine 80-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-15 30973961-7 2019 Moreover, NR4A1 depletion not only mimicked but also exaggerated the effects of Hcy on steatosis, whereas NR4A1 agonist Cytosporone B (CsnB) blocked Hcy-induced steatosis. cytosporone B 120-133 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-111 30973961-7 2019 Moreover, NR4A1 depletion not only mimicked but also exaggerated the effects of Hcy on steatosis, whereas NR4A1 agonist Cytosporone B (CsnB) blocked Hcy-induced steatosis. cytosporone B 135-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-111 30973961-7 2019 Moreover, NR4A1 depletion not only mimicked but also exaggerated the effects of Hcy on steatosis, whereas NR4A1 agonist Cytosporone B (CsnB) blocked Hcy-induced steatosis. Homocysteine 149-152 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-111 30973961-9 2019 Thus, Hcy transiently and rapidly induces NR4A1 expression to reduce Hcy-induced steatosis. Homocysteine 6-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-47 30973961-9 2019 Thus, Hcy transiently and rapidly induces NR4A1 expression to reduce Hcy-induced steatosis. Homocysteine 69-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-47 30610588-0 2019 Efficacy and safety of the combination of metformin, everolimus and exemestane in overweight and obese postmenopausal patients with metastatic, hormone receptor-positive, HER2-negative breast cancer: a phase II study. Metformin 42-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-160 30926635-4 2019 Here, we report our identification and characterization of DIM-C-pPhCF3 +MeSO3 - (BI1071), an oxidized product derived from indole-3-carbinol metabolite, as a modulator of the Nur77-Bcl-2 apoptotic pathway. 1,1-bis(3'-indolyl)-1-(4-trifluoromethylphenyl)methane 59-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 176-181 30926635-4 2019 Here, we report our identification and characterization of DIM-C-pPhCF3 +MeSO3 - (BI1071), an oxidized product derived from indole-3-carbinol metabolite, as a modulator of the Nur77-Bcl-2 apoptotic pathway. meso3 - 73-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 176-181 30926635-4 2019 Here, we report our identification and characterization of DIM-C-pPhCF3 +MeSO3 - (BI1071), an oxidized product derived from indole-3-carbinol metabolite, as a modulator of the Nur77-Bcl-2 apoptotic pathway. bi1071 82-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 176-181 30926635-4 2019 Here, we report our identification and characterization of DIM-C-pPhCF3 +MeSO3 - (BI1071), an oxidized product derived from indole-3-carbinol metabolite, as a modulator of the Nur77-Bcl-2 apoptotic pathway. indole-3-carbinol 124-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 176-181 30610588-0 2019 Efficacy and safety of the combination of metformin, everolimus and exemestane in overweight and obese postmenopausal patients with metastatic, hormone receptor-positive, HER2-negative breast cancer: a phase II study. exemestane 68-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-160 30610588-2 2019 Thus, we hypothesized that the addition of metformin to everolimus and exemestane, could lead to better outcomes in overweight and obese patients with metastatic, hormone receptor-positive, HER2-negative breast cancer. Metformin 43-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 163-179 30610588-2 2019 Thus, we hypothesized that the addition of metformin to everolimus and exemestane, could lead to better outcomes in overweight and obese patients with metastatic, hormone receptor-positive, HER2-negative breast cancer. Everolimus 56-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 163-179 30610588-2 2019 Thus, we hypothesized that the addition of metformin to everolimus and exemestane, could lead to better outcomes in overweight and obese patients with metastatic, hormone receptor-positive, HER2-negative breast cancer. exemestane 71-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 163-179 30610588-3 2019 We conducted a phase II trial to evaluate the efficacy and safety of the combination of metformin, everolimus and exemestane in overweight and obese postmenopausal women with metastatic, hormone receptor-positive, HER2-negative breast cancer. Metformin 88-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 187-203 30610588-3 2019 We conducted a phase II trial to evaluate the efficacy and safety of the combination of metformin, everolimus and exemestane in overweight and obese postmenopausal women with metastatic, hormone receptor-positive, HER2-negative breast cancer. Everolimus 99-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 187-203 30610588-3 2019 We conducted a phase II trial to evaluate the efficacy and safety of the combination of metformin, everolimus and exemestane in overweight and obese postmenopausal women with metastatic, hormone receptor-positive, HER2-negative breast cancer. exemestane 114-124 nuclear receptor subfamily 4 group A member 1 Homo sapiens 187-203 30610588-11 2019 Conclusion The combination of metformin, everolimus and exemestane was safe and had moderate clinical benefit in overweight and obese with patients metastatic, hormone receptor-positive, HER2-negative breast cancer. Metformin 30-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-176 30610588-11 2019 Conclusion The combination of metformin, everolimus and exemestane was safe and had moderate clinical benefit in overweight and obese with patients metastatic, hormone receptor-positive, HER2-negative breast cancer. Everolimus 41-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-176 30610588-11 2019 Conclusion The combination of metformin, everolimus and exemestane was safe and had moderate clinical benefit in overweight and obese with patients metastatic, hormone receptor-positive, HER2-negative breast cancer. exemestane 56-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-176 30798641-0 2019 Observational study of everolimus plus exemestane in postmenopausal women with hormone receptor-positive, HER2-negative advanced breast cancer. Everolimus 23-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-95 30806032-6 2019 To accelerate the drug development for non-smoking female NSCLC patients, we identified nilotinib as a potential agonist targeting NR4A1 encoded protein by molecular docking and molecular dynamic stimulation. nilotinib 88-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 131-136 30872732-0 2019 Pro-angiogenic Ginsenosides F1 and Rh1 Inhibit Vascular Leakage by Modulating NR4A1. Ginsenosides 15-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-83 30872732-0 2019 Pro-angiogenic Ginsenosides F1 and Rh1 Inhibit Vascular Leakage by Modulating NR4A1. 2,5-diaziridinyl-3-(hydroxymethyl)-6-methyl-1,4-benzoquinone 35-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-83 30798641-0 2019 Observational study of everolimus plus exemestane in postmenopausal women with hormone receptor-positive, HER2-negative advanced breast cancer. exemestane 39-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-95 30079740-7 2019 In combination with fulvestrant, CDK 4/6 inhibitors used for the treatment of hormone receptor-positive ABC resulted in a 43% to 58% improvement in median PFS versus fulvestrant alone. Fulvestrant 20-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-94 30912283-8 2019 Clamp-derived glucose disposal rates correlated with Nur77 (r2 = 0.14) and NOR1 (r2 = 0.12) protein expression responses to insulin, whereas age (Nur77: r2 = 0.22; NOR1: r2 = 0.25) and BMI (Nur77: r2 = 0.22; NOR1: r2 = 0.42) showed inverse correlations, corroborating preclinical data. Glucose 14-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-58 31011314-7 2019 We believe that anastrozole induced a change in the local estrogen level, which affected the hormone receptor-positive endothelial cells in the dermis near the primary lesion of the breast cancer and caused a cutaneous adverse event only in the aforementioned area. Anastrozole 16-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-109 30079740-7 2019 In combination with fulvestrant, CDK 4/6 inhibitors used for the treatment of hormone receptor-positive ABC resulted in a 43% to 58% improvement in median PFS versus fulvestrant alone. Fulvestrant 166-177 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-94 30478785-0 2019 G-protein-coupled estrogen receptor GPER-1 expression in hormone receptor-positive breast cancer is associated with poor benefit of tamoxifen. Tamoxifen 132-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-73 30607817-4 2019 This led to the approval of neratinib in the EU as extended adjuvant therapy for patients with early-stage HRc-positive, HER2-positive breast cancer and who are less than 1 year from completion of prior adjuvant trastuzumab-based therapy. neratinib 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-110 30252536-6 2019 Thus, HDAC inhibitors and RA-induced miR-22 resulted in simultaneous induction of cytoplasmic RARbeta and NUR77, leading to apoptosis of colon cancer cells. Tretinoin 26-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-111 30700929-0 2018 Exploratory clinical study of chidamide, an oral subtype-selective histone deacetylase inhibitor, in combination with exemestane in hormone receptor-positive advanced breast cancer. N-(2-amino-5-fluorobenzyl)-4-(N-(pyridine-3-acrylyl)aminomethyl)benzamide 30-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-148 30535552-0 2019 Correction to: Fulvestrant-Based Combination Therapy for Second-Line Treatment of Hormone Receptor-Positive Advanced Breast Cancer. Fulvestrant 15-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-98 30535552-1 2019 The article Fulvestrant-Based Combination Therapy for Second-Line Treatment of Hormone Receptor-Positive Advanced Breast Cancer, written by Sarah Sammons, Noah S. Kornblum and Kimberly L. Blackwell, was originally published electronically on the publisher"s internet portal (currently SpringerLink). Fulvestrant 12-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-95 30605443-10 2019 CONCLUSIONS These findings provide a rationale for future clinical trials of palbociclib and everolimus combination-based therapy in hormone receptor-positive breast cancer. Everolimus 93-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-149 29687661-12 2019 Hormone-receptor-positive breast cancer patients who receive adjuvant endocrine therapy with tamoxifen alone might be candidates for extended endocrine therapy. Tamoxifen 93-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 30588017-4 2018 Pooled pathological complete response (pCR) and 5-year disease-free survival (DFS) rates were higher for the neoadjuvant BEV + CT group (OR =1.37 [1.19, 1.58]; P<0.001 and HR =0.84 [0.72, 0.98]; P=0.020, respectively), but 5-year overall survival (OS) rate showed no significant difference (HR =0.79 [0.55, 1.11]; P=0.180). N-[(2z)-1,3-Thiazolidin-2-Ylidene]sulfamide 121-124 nuclear receptor subfamily 4 group A member 1 Homo sapiens 175-177 30588017-4 2018 Pooled pathological complete response (pCR) and 5-year disease-free survival (DFS) rates were higher for the neoadjuvant BEV + CT group (OR =1.37 [1.19, 1.58]; P<0.001 and HR =0.84 [0.72, 0.98]; P=0.020, respectively), but 5-year overall survival (OS) rate showed no significant difference (HR =0.79 [0.55, 1.11]; P=0.180). N-[(2z)-1,3-Thiazolidin-2-Ylidene]sulfamide 121-124 nuclear receptor subfamily 4 group A member 1 Homo sapiens 294-296 30588017-5 2018 Subgroup analysis showed that the pCR rate was significantly higher in both patients with hormone receptor (HR)-positive breast cancer (OR =1.30 [1.01, 1.66]; P=0.040) and those with HR-negative breast cancer (OR =1.52 [1.25, 1.83]; P<0.001) in BEV + CT group. bev + ct 248-256 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-106 30588017-5 2018 Subgroup analysis showed that the pCR rate was significantly higher in both patients with hormone receptor (HR)-positive breast cancer (OR =1.30 [1.01, 1.66]; P=0.040) and those with HR-negative breast cancer (OR =1.52 [1.25, 1.83]; P<0.001) in BEV + CT group. bev + ct 248-256 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-110 30588017-5 2018 Subgroup analysis showed that the pCR rate was significantly higher in both patients with hormone receptor (HR)-positive breast cancer (OR =1.30 [1.01, 1.66]; P=0.040) and those with HR-negative breast cancer (OR =1.52 [1.25, 1.83]; P<0.001) in BEV + CT group. bev + ct 248-256 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-185 30136059-0 2019 Fulvestrant-Based Combination Therapy for Second-Line Treatment of Hormone Receptor-Positive Advanced Breast Cancer. Fulvestrant 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-83 30136059-1 2019 Fulvestrant is recommended for patients with hormone receptor-positive (HR+) advanced breast cancer (ABC) who progress after aromatase inhibitor therapy. Fulvestrant 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-61 30605443-9 2019 Importantly, everolimus enhanced the antitumor effect of palbociclib in palbociclib-sensitive hormone receptor-positive cells (MCF-7 cells). Everolimus 13-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-110 30361875-9 2019 CONCLUSIONS: Metronomic oral capecitabine combined with AIs showed good efficacy, minimal toxicities, and good tolerance in HR-positive patients with ABC. Capecitabine 29-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 124-126 30700929-0 2018 Exploratory clinical study of chidamide, an oral subtype-selective histone deacetylase inhibitor, in combination with exemestane in hormone receptor-positive advanced breast cancer. exemestane 118-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-148 30536272-1 2018 Tamoxifen (TMX) is the main drug used both in pre and postmenopausal women as adjuvant treatment for hormone receptor-positive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 101-117 30032697-1 2018 OBJECTIVES: The combination of a cyclin-dependent kinase 4 and 6 (CDK 4/6) inhibitor with the aromatase inhibitor letrozole is a safe and effective alternative to letrozole monotherapy for first-line hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) breast cancer. Letrozole 114-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 200-216 30035646-1 2018 Letrozole (LTZ) is effective for the treatment of hormone-receptor-positive breast cancer in postmenopausal women. Letrozole 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-66 30035646-1 2018 Letrozole (LTZ) is effective for the treatment of hormone-receptor-positive breast cancer in postmenopausal women. Letrozole 11-14 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-66 30325029-3 2018 Based on these findings, we hypothesized that cytosporone-B (Csn-B), an NR4A1 agonist, may hold significant therapeutic potential. cytosporone B 46-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-77 30325029-3 2018 Based on these findings, we hypothesized that cytosporone-B (Csn-B), an NR4A1 agonist, may hold significant therapeutic potential. cytosporone B 61-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-77 30072581-2 2018 Moreover, TGFbeta-induced migration of the cells is also blocked by the nuclear export inhibitor leptomycin B (LMB) and the orphan nuclear receptor 4A1 (NR4A1) ligand 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (CDIM8), which retains NR4A1 in the nucleus. leptomycin B 97-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-242 30072581-2 2018 Moreover, TGFbeta-induced migration of the cells is also blocked by the nuclear export inhibitor leptomycin B (LMB) and the orphan nuclear receptor 4A1 (NR4A1) ligand 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (CDIM8), which retains NR4A1 in the nucleus. leptomycin B 111-114 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-242 30072581-2 2018 Moreover, TGFbeta-induced migration of the cells is also blocked by the nuclear export inhibitor leptomycin B (LMB) and the orphan nuclear receptor 4A1 (NR4A1) ligand 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (CDIM8), which retains NR4A1 in the nucleus. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 167-213 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-158 30072581-2 2018 Moreover, TGFbeta-induced migration of the cells is also blocked by the nuclear export inhibitor leptomycin B (LMB) and the orphan nuclear receptor 4A1 (NR4A1) ligand 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (CDIM8), which retains NR4A1 in the nucleus. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 167-213 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-242 30072581-2 2018 Moreover, TGFbeta-induced migration of the cells is also blocked by the nuclear export inhibitor leptomycin B (LMB) and the orphan nuclear receptor 4A1 (NR4A1) ligand 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (CDIM8), which retains NR4A1 in the nucleus. DIM-C-pPhOH 215-220 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-158 30072581-4 2018 Thus, NR4A1 also plays an integral role in mediating TGFbeta-induced lung cancer invasion, and the NR4A1 ligand CDIM8, which binds nuclear NR4A1, represents a novel therapeutic approach for TGFbeta-induced blocking of lung cancer migration/invasion. DIM-C-pPhOH 112-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-104 30072581-4 2018 Thus, NR4A1 also plays an integral role in mediating TGFbeta-induced lung cancer invasion, and the NR4A1 ligand CDIM8, which binds nuclear NR4A1, represents a novel therapeutic approach for TGFbeta-induced blocking of lung cancer migration/invasion. DIM-C-pPhOH 112-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-104 30536272-1 2018 Tamoxifen (TMX) is the main drug used both in pre and postmenopausal women as adjuvant treatment for hormone receptor-positive breast cancer. Tamoxifen 11-14 nuclear receptor subfamily 4 group A member 1 Homo sapiens 101-117 30568462-0 2018 A comparison of fulvestrant plus a targeted agent with fulvestrant alone in hormone receptor-positive advanced breast cancer that progressed on prior endocrine therapy: a meta-analysis. Fulvestrant 16-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-92 30568462-1 2018 Fulvestrant is recommended for the hormone receptor-positive metastatic breast cancer (MBC) patients progressed during or after prior endocrine therapy. Fulvestrant 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-51 30568462-12 2018 Taken together, combination of fulvestrant with a targeted agent, especially inhibitors targeting CDK4/6 or PI3K/mTOR pathway, may open a new avenue for more effective therapies in relapse or metastatic hormone receptor-positive breast cancer after prior aromatase inhibitors or tamoxifen treatment. Fulvestrant 31-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 203-219 29974356-0 2018 Efficacy and safety of fulvestrant in postmenopausal patients with hormone receptor-positive advanced breast cancer: a systematic literature review and meta-analysis. Fulvestrant 23-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-83 30555632-0 2018 Antitumor properties of Salvianolic acid B against triple-negative and hormone receptor-positive breast cancer cells via ceramide-mediated apoptosis. salvianolic acid B 24-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-87 29982165-0 2018 Molecular dynamics study of TMPA mediated dissociation of Nur77-LKB1 complex. trimethyl phosphate 28-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-63 29594945-3 2018 In the current study, we explored the effects of Nur77, an orphan nuclear receptor, on prostate cancer cell invasion following ADT. adt 127-130 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-54 30412117-11 2018 Women with hormone receptor (HR)-negative tumors were more likely to exhibit pCR than those with HR-positive tumors (P = .007).Decreased BPE of patients with HER2-positive breast cancer may serve as an indicator of NAC effectiveness. nac 215-218 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-27 29594945-6 2018 The effects of Nur77 over-expression and knockdown on ADT-induced prostate cancer cell invasion were characterized. adt 54-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-20 29594945-10 2018 Nur77 over-expression blocked invasion-promoting effect of ADT, which is consistent with the down-regulation of MMP9 and Snail protein expression. adt 59-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 29594945-13 2018 CONCLUSION: Considering the limited success of management of prostate cancer metastasis following ADT, our data strongly suggest that Nur77 regulation could be a promising direction for search of complementary therapeutic strategy on top of classic ADT therapy. adt 98-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 134-139 29594945-13 2018 CONCLUSION: Considering the limited success of management of prostate cancer metastasis following ADT, our data strongly suggest that Nur77 regulation could be a promising direction for search of complementary therapeutic strategy on top of classic ADT therapy. adt 249-252 nuclear receptor subfamily 4 group A member 1 Homo sapiens 134-139 30382056-0 2018 [Indoleamine 2,3-Dioxygenase Activity during Long-Term Letrozole Therapy for Hormone Receptor-Positive Breast Cancer]. Letrozole 55-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-93 29982165-4 2018 It is reported that the interaction of LKB1 with Nur77 is disrupted by the small molecular ligand TMPA (ethyl 2-[2,3,4-trimethoxy-6-(1-octanoyl)phenyl]acetate), such that the LKB1 is enabled to play its role in cytoplasm and further to regulate/reduce the blood glucose level. trimethyl phosphate 98-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-54 29982165-4 2018 It is reported that the interaction of LKB1 with Nur77 is disrupted by the small molecular ligand TMPA (ethyl 2-[2,3,4-trimethoxy-6-(1-octanoyl)phenyl]acetate), such that the LKB1 is enabled to play its role in cytoplasm and further to regulate/reduce the blood glucose level. ethyl 2-(2,3,4-trimethoxy-6-(1-octanoyl)phenyl)acetate 104-158 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-54 29982165-4 2018 It is reported that the interaction of LKB1 with Nur77 is disrupted by the small molecular ligand TMPA (ethyl 2-[2,3,4-trimethoxy-6-(1-octanoyl)phenyl]acetate), such that the LKB1 is enabled to play its role in cytoplasm and further to regulate/reduce the blood glucose level. Glucose 262-269 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-54 29982165-6 2018 The present study reveals that TMPAs induce an open-close motion of Nur77 which further decrease the stability of Nur77-LKB1 complex. trimethyl phosphate 31-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-73 29982165-6 2018 The present study reveals that TMPAs induce an open-close motion of Nur77 which further decrease the stability of Nur77-LKB1 complex. trimethyl phosphate 31-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-119 30312983-7 2018 The nodules corresponding to NIFTP were classified according to ACR as TR3 in 28.5% of cases, TR4 in 67.8%, and TR5 in only 3.5%. niftp 29-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-74 30412117-11 2018 Women with hormone receptor (HR)-negative tumors were more likely to exhibit pCR than those with HR-positive tumors (P = .007).Decreased BPE of patients with HER2-positive breast cancer may serve as an indicator of NAC effectiveness. nac 215-218 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-31 30111648-7 2018 C-DIM5 prevented nuclear export of Nur77 in astrocytes induced by MPTP treatment and simultaneously recruited Nurr1 to the nucleus, consistent with known transrepressive properties of this receptor. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine 66-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-40 30235292-7 2018 In previously endocrine therapy-treated postmenopausal patients with hormone-receptor positive advanced breast cancer, the PFS (HR = 0.77, 95%CI: 0.66-0.91) and ORR (RR = 1.78, 95%CI: 1.35-2.34) of combination therapy group were significantly higher than that from fulvestrant monotherapy group. Fulvestrant 265-276 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 29789969-0 2018 Identification of risk factors for toxicity in patients with hormone receptor-positive advanced breast cancer treated with bevacizumab plus letrozole: a CALGB 40503 (alliance) correlative study. Letrozole 140-149 nuclear receptor subfamily 4 group A member 1 Homo sapiens 61-77 29793946-0 2018 Phase II Study of Taselisib (GDC-0032) in Combination with Fulvestrant in Patients with HER2-Negative, Hormone Receptor-Positive Advanced Breast Cancer. 2-(3-(2-(1-isopropyl-3-methyl-1H-1,2-4-triazol-5-yl)-5,6-dihydrobenzo(f)imidazo(1,2-d)(1,4)oxazepin-9-yl)-1H-pyrazol-1-yl)-2-methylpropanamide 18-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-119 30075223-8 2018 In particular, we will focus our discussion on the FDA approved HDAC inhibitor valproic acid (VPA) which has been shown to alter proliferation, survival, cell migration, and hormone receptor expression of breast cancer cells in both the pre-clinical and clinical settings. Valproic Acid 79-92 nuclear receptor subfamily 4 group A member 1 Homo sapiens 174-190 30075223-8 2018 In particular, we will focus our discussion on the FDA approved HDAC inhibitor valproic acid (VPA) which has been shown to alter proliferation, survival, cell migration, and hormone receptor expression of breast cancer cells in both the pre-clinical and clinical settings. Valproic Acid 94-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 174-190 30233207-0 2018 Clinical benefit of fulvestrant monotherapy in the multimodal treatment of hormone receptor and HER2 positive advanced breast cancer: a case series. Fulvestrant 20-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 30202448-4 2018 Results: Palbociclib is indicated in combination with an aromatase inhibitor as initial endocrine therapy (ET) or with fulvestrant for patients with disease progression following ET for hormone receptor positive, human epidermal growth factor receptor 2 negative ABC or metastatic breast cancer. palbociclib 9-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 186-202 29789969-1 2018 BACKGROUND: In hormone receptor-positive advanced breast cancer, a progression-free survival benefit was reported with addition of bevacizumab to first-line letrozole. Letrozole 157-166 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-31 30130984-2 2018 The CDK4/6 inhibitor palbociclib in combination with endocrine therapy has been approved for treatment of HR-positive/HER2-negative breast cancer patients. palbociclib 21-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-108 29564714-2 2018 Palbociclib, a specific inhibitor of CDK4/6 with outstanding clinical efficacy data and limited toxicity, has been recently approved for the treatment of hormone receptor (HR)-positive human epidermal growth factor receptor 2 (HER2)-negative locally advanced or metastatic breast cancer, either in combination with an aromatase inhibitor or in combination with fulvestrant in women who have received prior endocrine therapy. palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-170 29564714-2 2018 Palbociclib, a specific inhibitor of CDK4/6 with outstanding clinical efficacy data and limited toxicity, has been recently approved for the treatment of hormone receptor (HR)-positive human epidermal growth factor receptor 2 (HER2)-negative locally advanced or metastatic breast cancer, either in combination with an aromatase inhibitor or in combination with fulvestrant in women who have received prior endocrine therapy. palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 172-174 30134173-4 2018 Nur77-deficient macrophages fail to downregulate IDH expression and accumulate higher levels of succinate and other TCA cycle-derived metabolites in response to inflammatory stimulation in a glutamine-independent manner. Succinic Acid 96-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 30134173-4 2018 Nur77-deficient macrophages fail to downregulate IDH expression and accumulate higher levels of succinate and other TCA cycle-derived metabolites in response to inflammatory stimulation in a glutamine-independent manner. Trichloroacetic Acid 116-119 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 30134173-4 2018 Nur77-deficient macrophages fail to downregulate IDH expression and accumulate higher levels of succinate and other TCA cycle-derived metabolites in response to inflammatory stimulation in a glutamine-independent manner. Glutamine 191-200 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 30123220-7 2018 Treatment of human moDCs with 6-mercaptopurine, an activator of Nur77, leads to diminished DC activation resulting in an impaired capacity to induce IFNgamma production by allogeneic T cells. Mercaptopurine 30-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-69 32914002-1 2018 Purpose: In the I-SPY 2 TRIAL (Investigation of Serial Studies to Predict Your Therapeutic Response With Imaging and Molecular Analysis 2), the pan-erythroblastic oncogene B inhibitor neratinib was available to all hormone receptor (HR)/human epidermal growth factor receptor 2 (HER2) subtypes and graduated in the HR-negative/HER2-positive signature. neratinib 184-193 nuclear receptor subfamily 4 group A member 1 Homo sapiens 215-231 32914002-1 2018 Purpose: In the I-SPY 2 TRIAL (Investigation of Serial Studies to Predict Your Therapeutic Response With Imaging and Molecular Analysis 2), the pan-erythroblastic oncogene B inhibitor neratinib was available to all hormone receptor (HR)/human epidermal growth factor receptor 2 (HER2) subtypes and graduated in the HR-negative/HER2-positive signature. neratinib 184-193 nuclear receptor subfamily 4 group A member 1 Homo sapiens 233-235 32914002-1 2018 Purpose: In the I-SPY 2 TRIAL (Investigation of Serial Studies to Predict Your Therapeutic Response With Imaging and Molecular Analysis 2), the pan-erythroblastic oncogene B inhibitor neratinib was available to all hormone receptor (HR)/human epidermal growth factor receptor 2 (HER2) subtypes and graduated in the HR-negative/HER2-positive signature. neratinib 184-193 nuclear receptor subfamily 4 group A member 1 Homo sapiens 315-317 29893769-1 2018 Background: The cyclin-dependent kinase 4 (CDK4)/6 inhibitor Palbociclib is a new standard treatment in hormone-receptor positive breast cancer patients. palbociclib 61-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 29731395-2 2018 Building upon the striking success of the combination of CDK4/6 inhibitors and the hormone receptor antagonist letrozole in breast cancer, many other combinations have recently entered clinical trials in multiple diseases. Letrozole 111-120 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-99 29786125-7 2018 The highest proportions and greatest increases in proportions of NAC were seen among triple-negative breast cancers (TNBC; 19.5-33.7%) and HER2+ (HR-/HER2+, 21.5-39.8%; HR+/HER2+, 17.0-33.7%) tumors. nac 65-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 146-148 29786125-10 2018 The highest use of NAC is in TNBC and HER2+ disease, with use in these subgroups being twice as frequent as in HR+/HER2- disease. nac 19-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-113 30111977-1 2018 Background: Oncotype dx [odx (Genomic Health, Redwood City, CA, U.S.A.)] is an approved prognostic tool for women with node-negative, hormone receptor-positive, her2-negative breast cancer. odx 25-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 134-150 29783894-0 2018 Fulvestrant in management of hormone receptor-positive metastatic breast cancer. Fulvestrant 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-45 30140215-1 2018 Everolimus is an effective treatment for advanced and/or metastatic breast cancer, especially in hormone receptor-positive cases. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-113 29437768-4 2018 An improvement in progression-free survival (PFS) was observed in patients receiving ribociclib plus letrozole compared with patients receiving placebo plus letrozole [HR = 0.556; 95% confidence interval (CI), 0.429-0.720]. Letrozole 101-110 nuclear receptor subfamily 4 group A member 1 Homo sapiens 168-170 29770955-0 2018 LAPTM4B gene copy number gain is associated with inferior response to anthracycline-based chemotherapy in hormone receptor negative breast carcinomas. Anthracyclines 70-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-122 29437768-4 2018 An improvement in progression-free survival (PFS) was observed in patients receiving ribociclib plus letrozole compared with patients receiving placebo plus letrozole [HR = 0.556; 95% confidence interval (CI), 0.429-0.720]. Letrozole 157-166 nuclear receptor subfamily 4 group A member 1 Homo sapiens 168-170 30358233-0 2018 Should addition of five years of ovarian suppression to tamoxifen be "must" for hormone receptor positive and HER-2 positive breast cancer under the age of 35? Tamoxifen 56-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-96 30197363-1 2018 Tamoxifen plays a critical role in the treatment of hormone receptor-positive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-68 29804902-1 2018 BACKGROUND: In MONALEESA-2, ribociclib plus letrozole showed improved progression-free survival compared with letrozole alone as first-line treatment for postmenopausal patients with hormone receptor (HR)-positive, HER2-negative, advanced breast cancer. Letrozole 44-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-199 29804902-1 2018 BACKGROUND: In MONALEESA-2, ribociclib plus letrozole showed improved progression-free survival compared with letrozole alone as first-line treatment for postmenopausal patients with hormone receptor (HR)-positive, HER2-negative, advanced breast cancer. Letrozole 44-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 201-203 30026420-1 2018 Several cases of hormone receptor-positive HER2-negative advanced and recurrent breast cancer treated with fulvestrant (FUL)were retrospectively investigated to assess the efficacy and safety of the treatment. Fulvestrant 107-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-33 29396664-9 2018 CONCLUSIONS: Eighty percent of HR-negative, HER2-positive breast cancers achieve pCR with paclitaxel/FEC neoadjuvant chemotherapy administered concomitantly with pertuzumab and trastuzumab. Paclitaxel 90-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-33 30013988-3 2018 Hyperfunction or dysfunction of NR4A1 is implicated in various metabolic processes, including carbohydrate metabolism, lipid metabolism, and energy balance, in major metabolic tissues, such as liver, skeletal muscle, pancreatic tissues, and adipose tissues. Carbohydrates 94-106 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-37 30013988-6 2018 And we focus on the physiological functions of NR4A1 receptor to the development of the metabolic diseases, with a special focus on the impact on carbohydrate and lipid metabolism in skeletal muscle, liver, adipose tissue, and islet. Carbohydrates 146-158 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-52 29963233-5 2018 Furthermore, we performed single cell analysis of cells from an estrogen dependent/hormone receptor-positive patient derived xenograft (PDX) tumor model treated with palbociclib. palbociclib 166-177 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-99 29116433-1 2018 BACKGROUND: Everolimus with exemestane has shown promising activity in patients with hormone-receptor (HR)-positive HER2-negative endocrine-resistant advanced breast cancer. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 29116433-1 2018 BACKGROUND: Everolimus with exemestane has shown promising activity in patients with hormone-receptor (HR)-positive HER2-negative endocrine-resistant advanced breast cancer. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-105 29116433-1 2018 BACKGROUND: Everolimus with exemestane has shown promising activity in patients with hormone-receptor (HR)-positive HER2-negative endocrine-resistant advanced breast cancer. exemestane 28-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 29116433-1 2018 BACKGROUND: Everolimus with exemestane has shown promising activity in patients with hormone-receptor (HR)-positive HER2-negative endocrine-resistant advanced breast cancer. exemestane 28-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-105 29397517-3 2018 We aimed to investigate metformin"s effects on proliferation, metastasis, and hormone receptor expressions in breast cancer cell line MCF-7 incubated in two different glucose conditions. Metformin 24-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-94 29861853-0 2018 Oxidized analogs of Di(1H-indol-3-yl)methyl-4-substituted benzenes are NR4A1-dependent UPR inducers with potent and safe anti-cancer activity. di(1h-indol-3-yl)methyl-4-substituted benzenes 20-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-76 29899843-6 2018 The Nur77 derived peptide preferentially induced apoptosis in paclitaxel-resistant cancer cells with high expression of Bcl-2. Paclitaxel 62-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-9 29861853-1 2018 Di(1H-indol-3-yl)(4-trifluoromethylphenyl)methane (DIM-Ph-4-CF3) is an analog of orphan nuclear receptor 4A1 (NR4A1) ligand cytosporone B. di(1h-indol-3-yl)(4-trifluoromethylphenyl)methane 0-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-115 29861853-1 2018 Di(1H-indol-3-yl)(4-trifluoromethylphenyl)methane (DIM-Ph-4-CF3) is an analog of orphan nuclear receptor 4A1 (NR4A1) ligand cytosporone B. dim-ph-4-cf3 51-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-115 29861853-1 2018 Di(1H-indol-3-yl)(4-trifluoromethylphenyl)methane (DIM-Ph-4-CF3) is an analog of orphan nuclear receptor 4A1 (NR4A1) ligand cytosporone B. cytosporone B 124-137 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-115 29861853-7 2018 Independently of DIM-Ph-4-CF3+ OMs-, the bulk of NR4A1 localized to the cytoplasm in various cancer cell lines, suggesting a cytoplasmic mechanism-of-action of DIM-Ph-4-CF3+ OMs- in UPR induction and cell death. dim-ph-4-cf3+ oms 160-177 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-54 29500843-0 2018 Phase I study of taselisib in Japanese patients with advanced solid tumors or hormone receptor-positive advanced breast cancer. 2-(3-(2-(1-isopropyl-3-methyl-1H-1,2-4-triazol-5-yl)-5,6-dihydrobenzo(f)imidazo(1,2-d)(1,4)oxazepin-9-yl)-1H-pyrazol-1-yl)-2-methylpropanamide 17-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-94 29700504-1 2018 Through the coupling of central and terminal naphthalene diimide functionalities, a unique non-fullerene electron acceptor, coded as N10, was designed, synthesized, characterized and applied in solution-processable bulk-heterojunction devices. naphthalenediimide 45-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-136 29700504-1 2018 Through the coupling of central and terminal naphthalene diimide functionalities, a unique non-fullerene electron acceptor, coded as N10, was designed, synthesized, characterized and applied in solution-processable bulk-heterojunction devices. Fullerenes 95-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-136 29700504-2 2018 The target N10 displayed good solubility, excellent thermal stability and energy levels complementing those of the conventional donor polymer poly(3-hexyl thiophene) (P3HT). polymer poly(3-hexyl thiophene) 134-165 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-14 29700504-2 2018 The target N10 displayed good solubility, excellent thermal stability and energy levels complementing those of the conventional donor polymer poly(3-hexyl thiophene) (P3HT). poly(3-hexylthiophene) 167-171 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-14 29700504-3 2018 An excellent power conversion efficiency of 7.65% was obtained in simple BHJ devices (P3HT : N10 1 : 1.2), which is the highest observed so far for NDI core-based non-fullerene acceptors. {(3S)-7-[(2-chloro-5-{5-(methylsulfonyl)-1-[3-(morpholin-4-yl)propyl]-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-3-yl}phenyl)ethynyl]-1,2,3,4-tetrahydroisoquinolin-3-yl}(piperidin-1-yl)methanone 73-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-96 29728098-0 2018 The 21-gene Recurrence Score assay predicts distant recurrence in lymph node-positive, hormone receptor-positive, breast cancer patients treated with adjuvant sequential epirubicin- and docetaxel-based or epirubicin-based chemotherapy (PACS-01 trial). Epirubicin 171-181 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-104 29728098-0 2018 The 21-gene Recurrence Score assay predicts distant recurrence in lymph node-positive, hormone receptor-positive, breast cancer patients treated with adjuvant sequential epirubicin- and docetaxel-based or epirubicin-based chemotherapy (PACS-01 trial). Docetaxel 187-196 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-104 29728098-0 2018 The 21-gene Recurrence Score assay predicts distant recurrence in lymph node-positive, hormone receptor-positive, breast cancer patients treated with adjuvant sequential epirubicin- and docetaxel-based or epirubicin-based chemotherapy (PACS-01 trial). Epirubicin 206-216 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-104 29414782-9 2018 Although an initial report has suggested that an unstructured loop region between the Bcl-2 BH4 and BH3 domains is required for Bcl-2"s interaction with Nur77/Nor-1, we found that it is dispensable for this interaction. sapropterin 92-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-158 29324303-1 2018 OBJECTIVES: The double-blind, phase III CONFIRM study (NCT00099437) evaluated fulvestrant 500 mg vs fulvestrant 250 mg in postmenopausal women with hormone receptor-positive locally advanced/metastatic breast cancer (LA/MBC). Fulvestrant 78-89 nuclear receptor subfamily 4 group A member 1 Homo sapiens 148-164 29247442-1 2018 BACKGROUND: Palbociclib, a CDK4-6 inhibitor, combined with endocrine therapy (ET) is a new standard of treatment for Hormone Receptor-positive Metastatic Breast Cancer. palbociclib 12-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 117-133 29138067-5 2018 RESULTS: In patients with HR-positive (HR+)/HER2-/NG-low tumors, regardless of change in tumor size, the loss of node positivity after NAC significantly improved disease-free survival (DFS). nac 135-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 26-28 29138067-5 2018 RESULTS: In patients with HR-positive (HR+)/HER2-/NG-low tumors, regardless of change in tumor size, the loss of node positivity after NAC significantly improved disease-free survival (DFS). nac 135-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-41 29138067-9 2018 CONCLUSION: Our results revealed that changes in tumor stage and nodal status after NAC might be prognostic markers in patients with HR+/HER2-/NG-high tumors or HR-/HER2- tumors, even if there are residual tumors in the breast. nac 84-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-135 29414782-11 2018 Bcl-2 alanine mutants at this region could no longer interact with Nur77/Nor-1 and could not initiate Nur77/Bcl-2-mediated cell death. Alanine 6-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-72 29501489-7 2018 Together, our results are the first to demonstrate that rApoptin was able to effectively induce breast cancer cell apoptosis both in vitro and in vivo and that this activity could be regulated by the phosphorylation of Nur77 and Akt and the mitochondrial pathway. rapoptin 56-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 219-224 29501489-0 2018 rApoptin induces apoptosis in human breast cancer cells via phosphorylation of Nur77 and Akt. rapoptin 0-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-84 29501489-5 2018 Furthermore, we found via western blot that rApoptin-induced apoptosis in MCF-7 and MDA-MB-231 cells was associated with the phosphorylation of Nur77 (p-Nur77) and Akt (p-Akt). rapoptin 44-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-149 29501489-5 2018 Furthermore, we found via western blot that rApoptin-induced apoptosis in MCF-7 and MDA-MB-231 cells was associated with the phosphorylation of Nur77 (p-Nur77) and Akt (p-Akt). rapoptin 44-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 151-158 29329000-4 2018 The SAR analysis revealed that C3-O-neoglycosides of digoxigenin exhibited stronger cytotoxicity and induction of Nur77 expression of tumor cells than C3-MeON-neoglycosides. c3-o-neoglycosides 31-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-119 29399694-4 2018 Inhibitors of CDK4/6 are presently the subjects of numerous studies, and PD 0332991, an inhibitor of CDK4/6, has been used to treat hormone receptor (HR)-positive, advanced-stage breast cancer. palbociclib 73-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-148 29399694-4 2018 Inhibitors of CDK4/6 are presently the subjects of numerous studies, and PD 0332991, an inhibitor of CDK4/6, has been used to treat hormone receptor (HR)-positive, advanced-stage breast cancer. palbociclib 73-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-152 29556076-0 2018 The Nuclear Orphan Receptor Nur77 Alleviates Palmitate-induced Fat Accumulation by Down-regulating G0S2 in HepG2 Cells. Palmitates 45-54 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 29556076-4 2018 Using human HepG2 hepatoma cells, this study aimed to investigate the functional role of Nur77 in palmitate-induced hepatic steatosis. Palmitates 98-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 29556076-6 2018 In addition, palmitate significantly suppressed Nur77 expression and stimulated the expression of peroxisome proliferator-activated receptor gamma (PPARgamma) and its target genes. Palmitates 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 29556076-7 2018 Nur77 overexpression significantly reduced palmitate-induced expression of PPARgamma and its target genes. Palmitates 43-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 29556076-8 2018 Moreover, Nur77 overexpression attenuated lipid accumulation and augmented lipolysis in palmitate-treated hepatocytes. Palmitates 88-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-15 29556076-10 2018 In summary, palmitate suppresses Nur77 expression in HepG2 cells, and Nur77 overexpression alleviates palmitate-induced hepatic fat accumulation by down-regulating G0S2. Palmitates 12-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-38 29556076-10 2018 In summary, palmitate suppresses Nur77 expression in HepG2 cells, and Nur77 overexpression alleviates palmitate-induced hepatic fat accumulation by down-regulating G0S2. Palmitates 102-111 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-75 29556076-11 2018 These results display a novel molecular mechanism linking Nur77-regulated G0S2 expression to palmitate-induced hepatic steatosis. Palmitates 93-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-63 29498706-4 2018 Based on the NR4A1 protein structure, 2-imino-6-methoxy-2H-chromene-3-carbothioamide (IMCA) was identified from the Specs compounds database using the protein structure-guided virtual screening approach. 2-Imino-6-methoxy-2H-chromene-3-carbothioamide 38-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 29329000-4 2018 The SAR analysis revealed that C3-O-neoglycosides of digoxigenin exhibited stronger cytotoxicity and induction of Nur77 expression of tumor cells than C3-MeON-neoglycosides. Digoxigenin 53-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-119 29329000-6 2018 Among them, 3beta-O-(beta-l-fucopyranosyl)-digoxigenin (3i) showed the highest activity on induction of Nur77 expression and translocation from the nucleus to cytoplasm, leading to cancer cell apoptosis. 3beta-o-(beta-l-fucopyranosyl)-digoxigenin 12-54 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-109 29207128-8 2018 Mechanistically, the overexpression of NR4A1 augmented caspase-9-dependent mitochondrial apoptosis, as evidenced by reduced mitochondrial membrane potential, reactive oxygen species (ROS) overproduction, mitochondrial permeability transition pore (mPTP) opening and the leakage of cytochrome c (Cyt-c) leakage. Reactive Oxygen Species 158-181 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 29124456-0 2018 Serial immunological parameters in a phase II trial of exemestane and low-dose oral cyclophosphamide in advanced hormone receptor-positive breast cancer. exemestane 55-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-129 29124456-0 2018 Serial immunological parameters in a phase II trial of exemestane and low-dose oral cyclophosphamide in advanced hormone receptor-positive breast cancer. Cyclophosphamide 84-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-129 29124456-4 2018 METHODS: This was a single-arm phase II trial of exemestane with cyclophosphamide in patients with metastatic HR-positive/HER2-negative breast cancer who had progressed on prior endocrine therapy (ClinicalTrials.gov: NCT01963481). exemestane 49-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-112 29177689-1 2018 PURPOSE: Hormone receptor (HR)-positive breast cancer (BC) shows a poor response to neoadjuvant chemotherapy (NACT). nact 110-114 nuclear receptor subfamily 4 group A member 1 Homo sapiens 9-25 29177689-1 2018 PURPOSE: Hormone receptor (HR)-positive breast cancer (BC) shows a poor response to neoadjuvant chemotherapy (NACT). nact 110-114 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-29 29207128-8 2018 Mechanistically, the overexpression of NR4A1 augmented caspase-9-dependent mitochondrial apoptosis, as evidenced by reduced mitochondrial membrane potential, reactive oxygen species (ROS) overproduction, mitochondrial permeability transition pore (mPTP) opening and the leakage of cytochrome c (Cyt-c) leakage. Reactive Oxygen Species 183-186 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 29423003-5 2018 We found that GATA4 and SF-1 were particularly critical for Leydig-specific markers expression and that GATA4, SF-1, and NGFI-B were necessary to generate functional iLCs that secreted testosterone. Testosterone 185-197 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-127 30415262-0 2018 Triclosan Suppresses Testicular Steroidogenesis via the miR-6321/JNK/ Nur77 Cascade. Triclosan 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-75 30147088-6 2018 The factors adversely affecting DFS in EBC were node metastasis (P < 0.001), higher metastatic nodes (P < 0.001), hormone receptor negativity (P = 0.001), and human epidermal growth factor receptor 2 (Her2neu) positivity (P = 0.033). NSC638702 39-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-136 30415262-10 2018 CONCLUSION: Taken together, the miR-6321/Map3k1-regulated JNK/c-Jun/ Nur77 cascade contributes to TCS-caused suppression of testicular steroidogenesis, and the decrease in 5alpha-Reductase expressions may be the compensatory mechanism. Triclosan 98-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-74 29270913-1 2018 Fulvestrant (Faslodex ), a selective estrogen receptor (ER) degrader, is now indicated for the treatment of ER+ or hormone-receptor positive (HR+)/HER2- advanced breast cancer in postmenopausal women previously untreated with endocrine therapy. Fulvestrant 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-131 29270913-1 2018 Fulvestrant (Faslodex ), a selective estrogen receptor (ER) degrader, is now indicated for the treatment of ER+ or hormone-receptor positive (HR+)/HER2- advanced breast cancer in postmenopausal women previously untreated with endocrine therapy. Fulvestrant 13-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-131 29371962-8 2017 Consistently, Oncomine analysis showed that NR4A1 was overexpressed in NSCLC tissues compared with normal tissues in published datasets (P < 0.001). oncomine 14-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-49 28981157-10 2018 Mechanistically, melatonin halted fission but recovered mitophagy via blockade of NR4A1/DNA-PKcs/p53 pathway, finally improving mitochondrial and liver function in the setting of NAFLD. Melatonin 17-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-87 28981157-12 2018 Meanwhile, we also confirm that melatonin has the ability to cut off the NR4A1/DNA-PKcs/p53 pathway, which confers a protective advantage to hepatocytes and mitochondria. Melatonin 32-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 73-78 28981157-13 2018 The manipulation of NR4A1/DNA-PKcs/p53 pathway by melatonin highlights a new entry point for treating NAFLD. Melatonin 50-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-25 30220928-0 2018 SABCS 2017: lifestyle factors, hormone receptor-positive advanced disease, liquid biopsies, and prognosis. sabcs 0-5 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-47 29353824-0 2018 Alcohol Consumption and Breast Cancer Risk According to Hormone Receptor Status in Japanese Women: A Case-Control Study. Alcohols 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 56-72 29269871-5 2017 Depolarization and cAMP signals induce preferential transcription of activity-dependent genes containing promoters with proximal CRE/TATA sequences, such as c-fos, Dusp1, Nr4a1, Nr4a2 and Ptgs2, but not genes with proximal CRE/TATA-less promoters (e.g. Nr4a3, Presenilin-1 and Presenilin-2). Cyclic AMP 19-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-176 29285035-3 2017 Clinical studies have suggested that everolimus combined with endocrine therapy prolongs progression-free survival in hormone receptor-positive breast cancer patients. Everolimus 37-47 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-134 29199269-4 2017 DDA is a partial agonist on liver-X-receptor (LXR) increasing Nur77, Nor1, and LC3 expression leading to autolysosome formation. 5-hydroxy-6-(2-(1H-imidazol-4-yl)ethylamino)cholestan-3-ol 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 28942098-8 2017 Age <50 years, breast MRI, large tumour size, advanced nodal disease, negative hormone receptor status and hospital participation in neoadjuvant clinical studies were significant independent predictors of NAC use (all P < 0.001). nac 208-211 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-98 29178841-9 2017 ST59-SCCmec IV-t437 (61.7%) was the most prevalent genotype of MRSA, and ST22-t309 (18.2%), ST5-t002 (9.1%), ST6-t701 (9.1%), ST188-t189 (9.1%) were the top four genotypes of methicillin-sensitive SA (MSSA). Methicillin 175-186 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-4 28778424-4 2017 Polyethylene oxide N10, a semicrystalline thermoplastic polymer (polyethylene oxide N10; Mol. Polyethylene Glycols 0-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-22 28778424-4 2017 Polyethylene oxide N10, a semicrystalline thermoplastic polymer (polyethylene oxide N10; Mol. Polyethylene Glycols 0-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-87 28778424-4 2017 Polyethylene oxide N10, a semicrystalline thermoplastic polymer (polyethylene oxide N10; Mol. Polyethylene Glycols 65-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-22 29178841-15 2017 The prevalence of the biofilm associated genes among ST59-SCCmec IV-t437 clone was: icaA (100.0%), icaD (97.3%), fnbpA (100.0%), fnbpB (0), clfA (100%), clfB (100%), cna (2.7%), bbp (0), ebpS (88.5%), sdrC (78.4%), sdrD (5.4%), and sdrE (94.5%). icaa 84-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-57 29178841-15 2017 The prevalence of the biofilm associated genes among ST59-SCCmec IV-t437 clone was: icaA (100.0%), icaD (97.3%), fnbpA (100.0%), fnbpB (0), clfA (100%), clfB (100%), cna (2.7%), bbp (0), ebpS (88.5%), sdrC (78.4%), sdrD (5.4%), and sdrE (94.5%). fnbpa 113-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-57 29178841-15 2017 The prevalence of the biofilm associated genes among ST59-SCCmec IV-t437 clone was: icaA (100.0%), icaD (97.3%), fnbpA (100.0%), fnbpB (0), clfA (100%), clfB (100%), cna (2.7%), bbp (0), ebpS (88.5%), sdrC (78.4%), sdrD (5.4%), and sdrE (94.5%). fnbpb 129-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-57 29178841-15 2017 The prevalence of the biofilm associated genes among ST59-SCCmec IV-t437 clone was: icaA (100.0%), icaD (97.3%), fnbpA (100.0%), fnbpB (0), clfA (100%), clfB (100%), cna (2.7%), bbp (0), ebpS (88.5%), sdrC (78.4%), sdrD (5.4%), and sdrE (94.5%). clfa 140-144 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-57 29178841-15 2017 The prevalence of the biofilm associated genes among ST59-SCCmec IV-t437 clone was: icaA (100.0%), icaD (97.3%), fnbpA (100.0%), fnbpB (0), clfA (100%), clfB (100%), cna (2.7%), bbp (0), ebpS (88.5%), sdrC (78.4%), sdrD (5.4%), and sdrE (94.5%). clfb 153-157 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-57 29178841-15 2017 The prevalence of the biofilm associated genes among ST59-SCCmec IV-t437 clone was: icaA (100.0%), icaD (97.3%), fnbpA (100.0%), fnbpB (0), clfA (100%), clfB (100%), cna (2.7%), bbp (0), ebpS (88.5%), sdrC (78.4%), sdrD (5.4%), and sdrE (94.5%). 4-boronic acid benzophenone 178-181 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-57 29178841-15 2017 The prevalence of the biofilm associated genes among ST59-SCCmec IV-t437 clone was: icaA (100.0%), icaD (97.3%), fnbpA (100.0%), fnbpB (0), clfA (100%), clfB (100%), cna (2.7%), bbp (0), ebpS (88.5%), sdrC (78.4%), sdrD (5.4%), and sdrE (94.5%). ebps 187-191 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-57 28885430-4 2017 Given the hormone receptor status and size of the tumor, the patient was initially treated with fulvestrant and goserelin acetate in an attempt to reduce the size of the mass. Fulvestrant 96-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-26 28872880-8 2017 Furthermore, the study also permitted the identification of ten novel prospective allosteric sites named NP1 to NP10, involving in most of the cases protein structural elements that control kinase activation including the activation loop, the catalytic loop, the alphaC helix, the L16 loop, and the glycine-rich loop. Glycine 299-306 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-116 28904441-1 2017 Recently, everolimus (Evl) has been introduced in the management of hormone receptor-positive metastatic breast cancer, in combination with aromatase inhibitors. Everolimus 10-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-84 28754437-2 2017 In the present study, we identified fangchinoline, a bisbenzyltetrahydroisoquinoline alkaloid from Stephania tetrandra, as a new inactivator of nuclear NR4A1 and demonstrated that fangchinoline inhibits cell proliferation and induces apoptosis, in part, via the NR4A1-dependent pro-apoptotic pathways in human pancreatic cancer cells. fangchinoline 180-193 nuclear receptor subfamily 4 group A member 1 Homo sapiens 262-267 28754437-4 2017 These results suggest that inhibition of NR4A1-mediated transcriptional activity was involved in the anticancer effects of fangchinoline, and fangchinoline represents a novel class of mechanism-based anticancer agents targeting NR4A1 that is overexpressed in pancreatic cancer. fangchinoline 123-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 28754437-4 2017 These results suggest that inhibition of NR4A1-mediated transcriptional activity was involved in the anticancer effects of fangchinoline, and fangchinoline represents a novel class of mechanism-based anticancer agents targeting NR4A1 that is overexpressed in pancreatic cancer. fangchinoline 123-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 228-233 28754437-4 2017 These results suggest that inhibition of NR4A1-mediated transcriptional activity was involved in the anticancer effects of fangchinoline, and fangchinoline represents a novel class of mechanism-based anticancer agents targeting NR4A1 that is overexpressed in pancreatic cancer. fangchinoline 142-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 228-233 28793767-0 2017 Ginsenoside 20(S)-Rh2 Induces Apoptosis and Differentiation of Acute Myeloid Leukemia Cells: Role of Orphan Nuclear Receptor Nur77. ginsenoside 20(s)-rh2 0-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-130 28793767-3 2017 In our study, 20(S)-Rh2 induced the expression of orphan nuclear receptor Nur77 and death receptor proteins Fas, FasL, DR5, and TRAIL, as well as the cleavage of caspase 8 and caspase 3 in HL-60 cells. rh2 20-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-79 28793767-5 2017 Meanwhile, 20(S)-Rh2 promoted Nur77 translocation from the nucleus to mitochondria and enhanced the interaction between Nur77 and Bcl-2, resulting in the exposure of the BH3 domain of Bcl-2 and activation of Bax. (s)-rh2 13-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-35 28793767-5 2017 Meanwhile, 20(S)-Rh2 promoted Nur77 translocation from the nucleus to mitochondria and enhanced the interaction between Nur77 and Bcl-2, resulting in the exposure of the BH3 domain of Bcl-2 and activation of Bax. (s)-rh2 13-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-125 28754437-0 2017 Inactivation of the orphan nuclear receptor NR4A1 contributes to apoptosis induction by fangchinoline in pancreatic cancer cells. fangchinoline 88-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-49 28754437-2 2017 In the present study, we identified fangchinoline, a bisbenzyltetrahydroisoquinoline alkaloid from Stephania tetrandra, as a new inactivator of nuclear NR4A1 and demonstrated that fangchinoline inhibits cell proliferation and induces apoptosis, in part, via the NR4A1-dependent pro-apoptotic pathways in human pancreatic cancer cells. fangchinoline 36-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 152-157 28754437-2 2017 In the present study, we identified fangchinoline, a bisbenzyltetrahydroisoquinoline alkaloid from Stephania tetrandra, as a new inactivator of nuclear NR4A1 and demonstrated that fangchinoline inhibits cell proliferation and induces apoptosis, in part, via the NR4A1-dependent pro-apoptotic pathways in human pancreatic cancer cells. fangchinoline 36-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 262-267 28754437-2 2017 In the present study, we identified fangchinoline, a bisbenzyltetrahydroisoquinoline alkaloid from Stephania tetrandra, as a new inactivator of nuclear NR4A1 and demonstrated that fangchinoline inhibits cell proliferation and induces apoptosis, in part, via the NR4A1-dependent pro-apoptotic pathways in human pancreatic cancer cells. bisbenzyltetrahydroisoquinoline alkaloid 53-93 nuclear receptor subfamily 4 group A member 1 Homo sapiens 152-157 28601930-8 2017 Within the HR-positive/Her2-negative subtype, more women received gonadotropin-releasing hormone agonist and tamoxifen treatment from 2003 to 2008 compared with 1989 to 2002 (p = 0.001 and p = 0.075, respectively). Tamoxifen 109-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-13 28601930-9 2017 CONCLUSIONS: HR-positive young breast cancer patients have a poorer survival compared with older patients, even with more frequent chemotherapy, but more recent use of tamoxifen and ovarian suppression might improve this outcome in these patients. Tamoxifen 168-177 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-15 28904441-1 2017 Recently, everolimus (Evl) has been introduced in the management of hormone receptor-positive metastatic breast cancer, in combination with aromatase inhibitors. Everolimus 22-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-84 28851309-0 2017 Differences in elongation of very long chain fatty acids and fatty acid metabolism between triple-negative and hormone receptor-positive breast cancer. long 16-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-127 28838387-7 2017 RESULTS AND CONCLUSION: The TR3 activator cytosporone B was used to investigate TR3-mediated apoptosis in NSCLC cells under normoxic and hypoxic conditions. cytosporone B 42-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-31 28838387-7 2017 RESULTS AND CONCLUSION: The TR3 activator cytosporone B was used to investigate TR3-mediated apoptosis in NSCLC cells under normoxic and hypoxic conditions. cytosporone B 42-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-83 28418095-4 2017 1,1-Bis(3"-indolyl)-1-(p-substituted phenyl)methane (C-DIM) compounds containing p-hydroxy (DIM-C-pPhOH) and p-carbomethoxy (DIM-C-pPhCO2 Me) groups are NR4A1 ligands that act as antagonists for this receptor. 1,1-bis(3"-indolyl)-1-(p-substituted phenyl)methane 0-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-158 28418095-4 2017 1,1-Bis(3"-indolyl)-1-(p-substituted phenyl)methane (C-DIM) compounds containing p-hydroxy (DIM-C-pPhOH) and p-carbomethoxy (DIM-C-pPhCO2 Me) groups are NR4A1 ligands that act as antagonists for this receptor. c-dim 53-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-158 28418095-5 2017 Treatment of pancreatic and colon cancer cells with DIM-C-pPhOH or DIM-C-pPhCO2 Me mimics the effects of NR4A1 knockdown and decreases beta1-integrin expression, beta1-integrin regulated genes and responses including migration and adhesion. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 52-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-110 28418095-5 2017 Treatment of pancreatic and colon cancer cells with DIM-C-pPhOH or DIM-C-pPhCO2 Me mimics the effects of NR4A1 knockdown and decreases beta1-integrin expression, beta1-integrin regulated genes and responses including migration and adhesion. p-carboxymethylphenyl 1,1-bis(3'-indolyl)-1-(p-carboxymethylphenyl)methane 67-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-110 28789401-0 2017 Long-term remission of hormone receptor-positive/HER2-positive metastatic breast cancer due to combined treatment with everolimus/trastuzumab/exemestane: A case report. Everolimus 119-129 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-39 28816294-1 2017 OBJECTIVE: To optimize and establish the best hydrolysis method of diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate through the optimization of simple compound of diethyl N-(4-aminobenzoyl)-L-glutamate. N-(4-aminobenzoyl)-L-glutamate 186-216 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-106 28816294-2 2017 METHODS: To increase the low yield of hydrolysis reaction of diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate due to the by-products and difficult purification, we studied the effect of NaOH and KOH, two kinds of alkalis, three concentrations between 0.175-1 mol/L and five types of reaction time involved in 20, 30, 60, 120 and 180 min on the common side chain diethyl N-(4-aminobenzoyl)-L-glutamate. Ether 61-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-100 28816294-2 2017 METHODS: To increase the low yield of hydrolysis reaction of diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate due to the by-products and difficult purification, we studied the effect of NaOH and KOH, two kinds of alkalis, three concentrations between 0.175-1 mol/L and five types of reaction time involved in 20, 30, 60, 120 and 180 min on the common side chain diethyl N-(4-aminobenzoyl)-L-glutamate. Sodium Hydroxide 201-205 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-100 28816294-2 2017 METHODS: To increase the low yield of hydrolysis reaction of diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate due to the by-products and difficult purification, we studied the effect of NaOH and KOH, two kinds of alkalis, three concentrations between 0.175-1 mol/L and five types of reaction time involved in 20, 30, 60, 120 and 180 min on the common side chain diethyl N-(4-aminobenzoyl)-L-glutamate. potassium hydroxide 210-213 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-100 28816294-2 2017 METHODS: To increase the low yield of hydrolysis reaction of diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate due to the by-products and difficult purification, we studied the effect of NaOH and KOH, two kinds of alkalis, three concentrations between 0.175-1 mol/L and five types of reaction time involved in 20, 30, 60, 120 and 180 min on the common side chain diethyl N-(4-aminobenzoyl)-L-glutamate. N-(4-Aminobenzoyl)-L-glutamic acid diethyl ester 377-415 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-100 28816294-4 2017 Finally, on the basis of the best hydrolysis method of diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate, we completed the optimization of the hydrolysis reaction conditions of diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate. Ether 55-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-94 28816294-4 2017 Finally, on the basis of the best hydrolysis method of diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate, we completed the optimization of the hydrolysis reaction conditions of diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate. Ether 55-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 227-230 28816294-6 2017 The results indicated that treated with the optimized condition of 0.3 mol/L KOH in 60 min at the room temperature, diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate was converted into its diacid derivative in 95.6 % yield, which turned to be a better reaction condition compared with the previous reaction condition. potassium hydroxide 77-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 152-155 28816294-6 2017 The results indicated that treated with the optimized condition of 0.3 mol/L KOH in 60 min at the room temperature, diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate was converted into its diacid derivative in 95.6 % yield, which turned to be a better reaction condition compared with the previous reaction condition. diethyl ester 4-amino-n5-formyl-n8 116-150 nuclear receptor subfamily 4 group A member 1 Homo sapiens 152-155 28816294-6 2017 The results indicated that treated with the optimized condition of 0.3 mol/L KOH in 60 min at the room temperature, diethyl ester 4-amino-N5-formyl-N8, N10-dideazatetrahydrofolate was converted into its diacid derivative in 95.6 % yield, which turned to be a better reaction condition compared with the previous reaction condition. CARBROMAL 203-209 nuclear receptor subfamily 4 group A member 1 Homo sapiens 152-155 28818208-8 2017 RESULTS: Enhanced beta-adrenergic signaling in TTS-iPSC-CMs under catecholamine-induced stress increased expression of the cardiac stress marker NR4A1; cyclic adenosine monophosphate levels; and cyclic adenosine monophosphate-dependent protein kinase A-mediated hyperphosphorylation of RYR2-S2808, PLN-S16, TNI-S23/24, and Cav1.2-S1928, and leads to a reduced calcium time to transient 50% decay. Catecholamines 66-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-150 28633895-8 2017 Moreover, some MeON-neoglycosides (2b and 8b) could significant induce the expression of Nur77 and its translocation from the nucleus to cytoplasm. meon-neoglycosides 15-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 28515111-4 2017 Among those with hormone receptor-positive cancer, 74.8% initiated AET compared with 5.6% of women with negative and 54.0% with unknown-receptor status. 2-(2-Aminoethyl)isothiourea dihydrobromide 67-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-33 28515111-9 2017 Discontinuing treatment was associated with higher risk of all-cause and cancer-specific mortality regardless of hormone receptor status.Impact: This study underscores the need to study factors that influence discontinuation and the survival benefits of receiving AET for hormone receptor-negative breast cancer. 2-(2-Aminoethyl)isothiourea dihydrobromide 264-267 nuclear receptor subfamily 4 group A member 1 Homo sapiens 272-288 28789401-0 2017 Long-term remission of hormone receptor-positive/HER2-positive metastatic breast cancer due to combined treatment with everolimus/trastuzumab/exemestane: A case report. exemestane 142-152 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-39 28025696-0 2017 Influence of vitamin D signaling on hormone receptor status and HER2 expression in breast cancer. Vitamin D 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 36-52 28770167-1 2017 A 60- to 65-year-old female on prior statin therapy was initiated on palbociclib and fulvestrant for the treatment of metastatic, hormone-receptor positive breast cancer. Fulvestrant 85-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 130-146 28785180-2 2017 5 years of tamoxifen or an aromatase inhibitor for all patients with HR-positive early breast cancer is considered standard; however, there are now data to support an extended approach using up to 10 years of treatment. Tamoxifen 11-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-71 29050237-3 2017 In this study, we examined the regulation of the Nur77-Bcl-2 pathway by CCE9, a xanthone compound. cce9 72-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-54 29050237-3 2017 In this study, we examined the regulation of the Nur77-Bcl-2 pathway by CCE9, a xanthone compound. xanthone 80-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-54 29050237-6 2017 Inhibition of p38alpha MAPK activation by knocking down or knocking out p38alpha MAPK impaired the effect of CCE9 on inducing apoptosis and the expression and cytoplasmic localization of Nur77. cce9 109-113 nuclear receptor subfamily 4 group A member 1 Homo sapiens 187-192 28195993-1 2017 OBJECTIVE: Hormone receptor-positive breast cancers respond favorably to subcutaneous testosterone combined with an aromatase inhibitor. Testosterone 86-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-27 28576675-0 2017 Buparlisib plus fulvestrant versus placebo plus fulvestrant in postmenopausal, hormone receptor-positive, HER2-negative, advanced breast cancer (BELLE-2): a randomised, double-blind, placebo-controlled, phase 3 trial. NVP-BKM120 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-95 28195993-4 2017 METHODS: A 51-year-old woman on testosterone replacement therapy was diagnosed with hormone receptor-positive invasive breast cancer. Testosterone 32-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-100 27627986-3 2017 METHODS: The EvAluate-TM study is a prospective, multicenter noninterventional study in which treatment with the aromatase inhibitor letrozole was evaluated in postmenopausal women with hormone receptor-positive primary breast cancer. Letrozole 133-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 186-202 28978063-2 2017 Hormone receptor expression can also be found in MIBC, reflecting luminal and basal subtypes of breast cancer. 4-METHYL-2-PENTANOL 49-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 28324247-0 2017 Fulvestrant plus targeted agents versus fulvestrant alone for treatment of hormone-receptor positive advanced breast cancer progressed on previous endocrine therapy: a meta-analysis of randomized controlled trials. Fulvestrant 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 28422735-9 2017 Particularly, Oct4 expression was associated with poor clinical outcome in patients with hormone receptor-positive breast cancer treated with tamoxifen. Tamoxifen 142-151 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-105 28281345-1 2017 Photoinduced dehalogenation of the antifungal drug itraconazole (ITR) in acetonitrile (ACN) and ACN/water mixed solutions was investigated using femtosecond and nanosecond time-resolved transient absorption (fs-TA and ns-TA, respectively) and nanosecond time-resolved resonance Raman spectroscopy (ns-TR3) experiments. Itraconazole 51-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 301-304 28431397-6 2017 Importantly, Z-ligustilide-mediated autophagy inhibition restored Nur77 expression in MCF-7TR5 cells. ligustilide 13-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-71 28431397-7 2017 Furthermore, Z-ligustilide promoted the interaction of Nur77 with Ku80 and thereby abolished the association of DNA-PKcs with DNA ends. ligustilide 13-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 55-60 28281345-1 2017 Photoinduced dehalogenation of the antifungal drug itraconazole (ITR) in acetonitrile (ACN) and ACN/water mixed solutions was investigated using femtosecond and nanosecond time-resolved transient absorption (fs-TA and ns-TA, respectively) and nanosecond time-resolved resonance Raman spectroscopy (ns-TR3) experiments. Itraconazole 65-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 301-304 28281345-6 2017 The ns-TA and ns-TR3 results also provide some evidence that radical intermediates are generated through a homolytic carbon-halogen bond cleavage via predominantly the singlet excited state pathway in ACN but via mainly the triplet state pathway in the aqueous solutions. Carbon 117-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-20 28281345-6 2017 The ns-TA and ns-TR3 results also provide some evidence that radical intermediates are generated through a homolytic carbon-halogen bond cleavage via predominantly the singlet excited state pathway in ACN but via mainly the triplet state pathway in the aqueous solutions. Halogens 124-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-20 28281345-6 2017 The ns-TA and ns-TR3 results also provide some evidence that radical intermediates are generated through a homolytic carbon-halogen bond cleavage via predominantly the singlet excited state pathway in ACN but via mainly the triplet state pathway in the aqueous solutions. acetonitrile 201-204 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-20 28337303-11 2017 Inhibiting p38 by SB203580 could decrease TNF-induced NR4A1 to some extent, while inhibiting JNK could not. SB 203580 18-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-59 28388439-0 2017 Celastrol-Induced Nur77 Interaction with TRAF2 Alleviates Inflammation by Promoting Mitochondrial Ubiquitination and Autophagy. celastrol 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-23 28388439-3 2017 Here, we report that celastrol, a potent anti-inflammatory pentacyclic triterpene, binds Nur77 to inhibit inflammation and induce autophagy in a Nur77-dependent manner. celastrol 21-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 28388439-3 2017 Here, we report that celastrol, a potent anti-inflammatory pentacyclic triterpene, binds Nur77 to inhibit inflammation and induce autophagy in a Nur77-dependent manner. celastrol 21-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-150 28388439-3 2017 Here, we report that celastrol, a potent anti-inflammatory pentacyclic triterpene, binds Nur77 to inhibit inflammation and induce autophagy in a Nur77-dependent manner. Triterpenes 71-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 28388439-4 2017 Celastrol promotes Nur77 translocation from the nucleus to mitochondria, where it interacts with tumor necrosis factor receptor-associated factor 2 (TRAF2), a scaffold protein and E3 ubiquitin ligase important for inflammatory signaling. celastrol 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-24 28388439-7 2017 Together, our results identify Nur77 as a critical intracellular target for celastrol and unravel a mechanism of Nur77-dependent clearance of inflamed mitochondria to alleviate inflammation. celastrol 76-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-36 28049055-5 2017 In this work, a dual-inhibitor system containing EGCG and negatively charged polymeric nanoparticles (NP10), which was also demonstrated effective on the inhibition of Abeta aggregation, was developed and comprehensively studied by extensive biophysical and biological assays. epigallocatechin gallate 49-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-106 28049055-10 2017 NP10 might also help EGCG binding to Abeta, leading to its enhanced inhibitory effects on fibril elongation and secondary nucleation. epigallocatechin gallate 21-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-4 28293118-1 2017 INTRODUCTION AND AIMS: Tamoxifen is an adjuvant drug effective in treating hormone receptor - positive breast cancer. Tamoxifen 23-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 27554482-0 2017 Efficacy of Letrozole as First-Line Treatment of Postmenopausal Women with Hormone Receptor-Positive Metastatic Breast Cancer in Korea. Letrozole 12-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 27554482-4 2017 MATERIALS AND METHODS: This study retrospectively analyzed 84 HR-positive MBC patients who had been treated with letrozole from January 2001 to December 2012. Letrozole 113-122 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-64 27864345-4 2017 Similarly, cell treatment with the NR4A1 small-molecule antagonists 1,1-bis(3-indolyl)-1-(p-hydroxy or p-carbomethoxyphenyl)methane (C-DIM) decreased PAX3-FOXO1A. 1,1-bis(3-indolyl)-1-(p-hydroxy or p-carbomethoxyphenyl)methane 68-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-40 27864345-4 2017 Similarly, cell treatment with the NR4A1 small-molecule antagonists 1,1-bis(3-indolyl)-1-(p-hydroxy or p-carbomethoxyphenyl)methane (C-DIM) decreased PAX3-FOXO1A. Carbon 133-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-40 28203301-6 2017 Based on results of randomized clinical trials, palbociclib was granted accelerated approval by the US Food and Drug Administration (FDA) for use in combination with letrozole as initial endocrine-based therapy for metastatic disease in postmenopausal women with HR-positive, HER2-negative breast cancer, and was approved for use in combination with fulvestrant in women with HR-positive, HER2-negative advanced breast cancer with disease progression following endocrine therapy. palbociclib 48-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 263-265 28007942-1 2017 In a phase II trial, the mTOR inhibitor everolimus, combined with the endocrine therapy fulvestrant, improved progression-free survival in postmenopausal women with hormone receptor-positive, HER2-negative metastatic breast cancer who had become resistant to aromatase inhibitors. Everolimus 40-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 165-181 27826831-0 2017 Phase 1b study of orteronel in postmenopausal women with hormone-receptor positive (HR+) metastatic breast cancer. orteronel 18-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-73 27826831-3 2017 Thus, we conducted a phase 1b study of orteronel in postmenopausal women with hormone-receptor positive (HR+) metastatic breast cancer. orteronel 39-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-94 28203301-6 2017 Based on results of randomized clinical trials, palbociclib was granted accelerated approval by the US Food and Drug Administration (FDA) for use in combination with letrozole as initial endocrine-based therapy for metastatic disease in postmenopausal women with HR-positive, HER2-negative breast cancer, and was approved for use in combination with fulvestrant in women with HR-positive, HER2-negative advanced breast cancer with disease progression following endocrine therapy. palbociclib 48-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 376-378 27815995-0 2017 Impairment of the executive attention network in premenopausal women with hormone receptor-positive breast cancer treated with tamoxifen. Tamoxifen 127-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-90 28072715-8 2017 Three-year CDFS increased continuously each year after 1 year of DFS in hormone receptor (HR)-negative patients but decreased each year in HR-positive patients.In HR-positive patients who are disease free after 3 years, continuous care including surveillance and metastases workup should be considered, although this is not recommended in the current guidelines. cdfs 11-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-88 28072715-8 2017 Three-year CDFS increased continuously each year after 1 year of DFS in hormone receptor (HR)-negative patients but decreased each year in HR-positive patients.In HR-positive patients who are disease free after 3 years, continuous care including surveillance and metastases workup should be considered, although this is not recommended in the current guidelines. cdfs 11-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-92 27811009-5 2017 alpha6- and beta4-integrins as well as alpha5- and beta1-integrins are Sp-regulated genes that are also coregulated by the orphan nuclear receptor NR4A1 and these integrins can be targeted by agents such as penfluridol that suppress Sp1, Sp3, and Sp4 and also by NR4A1 antagonists. Penfluridol 207-218 nuclear receptor subfamily 4 group A member 1 Homo sapiens 147-152 27746162-0 2017 Diminished DYRK2 sensitizes hormone receptor-positive breast cancer to everolimus by the escape from degrading mTOR. Everolimus 71-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-44 27746162-1 2017 Mammalian target of rapamycin (mTOR) inhibitor, everolimus, provides benefit for metastatic hormone receptor positive breast cancer after failure of the endocrine therapy. Everolimus 48-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-108 27908454-15 2016 INTERPRETATION: Fulvestrant has superior efficacy and is a preferred treatment option for patients with hormone receptor-positive locally advanced or metastatic breast cancer who have not received previous endocrine therapy compared with a third-generation aromatase inhibitor, a standard of care for first-line treatment of these patients. Fulvestrant 16-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 27573562-0 2016 Pictilisib PI3Kinase inhibitor (a phosphatidylinositol 3-kinase [PI3K] inhibitor) plus paclitaxel for the treatment of hormone receptor-positive, HER2-negative, locally recurrent, or metastatic breast cancer: interim analysis of the multicentre, placebo-controlled, phase II randomised PEGGY study. 2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidine 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-135 27388585-10 2016 PIK3CA, PTEN, and AKT1 mutations occurred more frequently in the presence of hormone receptor overexpression (androgen, progesterone, or estrogen receptor). Progesterone 120-132 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-93 27876882-3 2016 Here, we showed that NR4A1 protein was predominantly expressed in neurons and up-regulated in patients with epilepsy as well as pilocarpine-induced mouse epileptic models. Pilocarpine 128-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 21-26 27717303-13 2016 CONCLUSIONS: Among patients receiving initial systemic treatment for HR-positive, HER2-negative advanced breast cancer, the duration of progression-free survival was significantly longer among those receiving ribociclib plus letrozole than among those receiving placebo plus letrozole, with a higher rate of myelosuppression in the ribociclib group. Letrozole 225-234 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-71 27723330-6 2016 The ns-TR3 and density functional theory (DFT) computational results were compared, and this indicates the binol moiety and water molecules both have important roles in the characteristics and structure of the key reactive BQM intermediate produced from BQMP-b. BINOL, naphthol 107-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 7-10 27723330-6 2016 The ns-TR3 and density functional theory (DFT) computational results were compared, and this indicates the binol moiety and water molecules both have important roles in the characteristics and structure of the key reactive BQM intermediate produced from BQMP-b. Water 124-129 nuclear receptor subfamily 4 group A member 1 Homo sapiens 7-10 27819368-1 2016 A tumor active targeting beta-cyclodextrin based nanocarrier beta-NC-OEI-SS-FA was designed by the modification of star shaped cationic derivatives beta-NC-OEI with folic acid through a disulfide bond, to co-deliver chemotherapeutic paclitaxel and the Nur77 gene for overcoming Bcl-2 mediated non-pump resistance by an "enemy to friend" strategy for potential drug resistant cancer therapy. betadex 25-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 252-257 27435628-5 2016 For example, in 2013 the European Medicines Agency approved the combination of lapatinib and trastuzumab in HER-2+/HR- patients. Lapatinib 79-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-117 27644246-8 2016 Furthermore, RNA sequencing analysis revealed GABA-induced changes in the mRNA expression of 30 genes, including EGR1, MAPK4, NR4A1, Fos, and FosB, in all the three types of CCC. gamma-Aminobutyric Acid 46-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-131 27663436-1 2016 PURPOSE: The purpose of this study is to evaluate survival outcome in patients with hormone receptor (HR)-positive (+) metastatic breast cancer (MBC) who received fluoxymesterone after disease progression while receiving contemporary hormonal therapy, as well as the association between estrogen receptor (ER)/androgen receptor (AR) status and survival outcome in these patients. Fluoxymesterone 163-178 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-100 27663436-1 2016 PURPOSE: The purpose of this study is to evaluate survival outcome in patients with hormone receptor (HR)-positive (+) metastatic breast cancer (MBC) who received fluoxymesterone after disease progression while receiving contemporary hormonal therapy, as well as the association between estrogen receptor (ER)/androgen receptor (AR) status and survival outcome in these patients. Fluoxymesterone 163-178 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-104 27663436-2 2016 METHODS: We retrospectively identified 103 patients treated with fluoxymesterone for HR + MBC from 2000 to 2014 and with at least one previous hormonal therapy in a metastatic setting. Fluoxymesterone 65-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-87 27644246-10 2016 The data suggest that GABA inhibits colon cancer cell proliferation perhaps by attenuating EGR1-NR4A1 axis, EGR1-Fos axis, and by disrupting MEK-EGR1 signaling pathway. gamma-Aminobutyric Acid 22-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-101 27281556-0 2016 Prognostic Value of Intrinsic Subtypes in Hormone Receptor-Positive Metastatic Breast Cancer Treated With Letrozole With or Without Lapatinib. Letrozole 106-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-58 27407089-0 2016 FDA Approval of Palbociclib in Combination with Fulvestrant for the Treatment of Hormone Receptor-Positive, HER2-Negative Metastatic Breast Cancer. palbociclib 16-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 27407089-1 2016 On February 19, 2016, the FDA approved palbociclib (Ibrance, Pfizer) for use in combination with fulvestrant (Faslodex, AstraZeneca) for the treatment of women with hormone receptor (HR)-positive, HER2-negative advanced or metastatic breast cancer (MBC) with disease progression following endocrine therapy. palbociclib 39-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 165-181 27407089-1 2016 On February 19, 2016, the FDA approved palbociclib (Ibrance, Pfizer) for use in combination with fulvestrant (Faslodex, AstraZeneca) for the treatment of women with hormone receptor (HR)-positive, HER2-negative advanced or metastatic breast cancer (MBC) with disease progression following endocrine therapy. palbociclib 39-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-185 27407089-5 2016 A statistically significant and clinically meaningful improvement in PFS (9.5 months vs. 4.6 months) was observed in patients receiving palbociclib plus fulvestrant [HR 0.46; 95% confidence interval (CI), 0.36-0.59; P < 0.0001]. palbociclib 136-147 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-168 27407089-5 2016 A statistically significant and clinically meaningful improvement in PFS (9.5 months vs. 4.6 months) was observed in patients receiving palbociclib plus fulvestrant [HR 0.46; 95% confidence interval (CI), 0.36-0.59; P < 0.0001]. Fulvestrant 153-164 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-168 27325862-0 2016 Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00. Methotrexate 35-47 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-80 27281556-0 2016 Prognostic Value of Intrinsic Subtypes in Hormone Receptor-Positive Metastatic Breast Cancer Treated With Letrozole With or Without Lapatinib. Lapatinib 132-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-58 27281556-15 2016 Patients with HR-positive/HER2-negative disease with a HER2-enriched profile may benefit from lapatinib in combination with endocrine therapy. Lapatinib 94-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-16 27368881-0 2016 Palbociclib in Combination With Fulvestrant in Women With Hormone Receptor-Positive/HER2-Negative Advanced Metastatic Breast Cancer: Detailed Safety Analysis From a Multicenter, Randomized, Placebo-Controlled, Phase III Study (PALOMA-3). palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-74 27368881-15 2016 IMPLICATIONS FOR PRACTICE: Treatment with palbociclib in combination with fulvestrant was generally safe and well-tolerated in patients with hormone receptor (HR)-positive metastatic breast cancer. palbociclib 42-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 141-157 27368881-15 2016 IMPLICATIONS FOR PRACTICE: Treatment with palbociclib in combination with fulvestrant was generally safe and well-tolerated in patients with hormone receptor (HR)-positive metastatic breast cancer. palbociclib 42-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-161 27506945-8 2016 Compared with HR-negative tumor, HR-positive tumor had significantly better response to sunitinib (p = 0.035). Sunitinib 88-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-35 27651692-3 2016 A change in hormone receptor status after neoadjuvant chemotherapy (NACT) has important therapeutic and prognostic consequences. nact 68-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-28 27117241-0 2016 Adjuvant Surgical Oophorectomy Plus Tamoxifen in Premenopausal Women With Operable Hormone Receptor-Positive Breast Cancer: A Global Treatment Option. Tamoxifen 36-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-99 27518192-6 2016 In comparison, TR3 (Rubescin D), a limonoid isolated in parallel and structurally highly similar to TR4 and TR9, did not interfere with hepatoma cell viability. rubescin d 20-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-18 28244487-10 2016 CONCLUSIONS: Everolimus based treatment has meaningful activity in heavily pretreated patients with HR-positive MBC but is associated with considerable toxicity and requirement for dose adjustment. Everolimus 13-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 100-102 27210004-4 2016 Everolimus has been approved in combination with exemestane for the treatment of hormone-receptor-positive advanced breast cancer after failure of nonsteroidal aromatase inhibitor therapy. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 27210004-4 2016 Everolimus has been approved in combination with exemestane for the treatment of hormone-receptor-positive advanced breast cancer after failure of nonsteroidal aromatase inhibitor therapy. exemestane 49-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 27150036-1 2016 Our recent finding that paclitaxel behaves as a peptidomimetic of the endogenous protein Nur77 inspired the design of two peptides (PEP1 and PEP2) reproducing the effects of paclitaxel on Bcl-2 and tubulin, proving the peptidomimetic nature of paclitaxel. Paclitaxel 24-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 27150036-1 2016 Our recent finding that paclitaxel behaves as a peptidomimetic of the endogenous protein Nur77 inspired the design of two peptides (PEP1 and PEP2) reproducing the effects of paclitaxel on Bcl-2 and tubulin, proving the peptidomimetic nature of paclitaxel. Paclitaxel 174-184 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 27150036-1 2016 Our recent finding that paclitaxel behaves as a peptidomimetic of the endogenous protein Nur77 inspired the design of two peptides (PEP1 and PEP2) reproducing the effects of paclitaxel on Bcl-2 and tubulin, proving the peptidomimetic nature of paclitaxel. Paclitaxel 174-184 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 27430727-8 2016 Importantly, we found that either knockdown of Nr4a1 or 3, 3"- Diindolylmethane (DIM), an Nr4a1 antagonist, were able to rescue the effects of SNRPN knockdown on neurite outgrowth of embryonic cortical neurons, providing the potential therapeutic methods for SNRPN deletion disorders. 3,3'-diindolylmethane 56-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-95 27406346-11 2016 RESULTS: Neratinib reached the prespecified efficacy threshold with regard to the HER2-positive, hormone-receptor-negative signature. neratinib 9-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-113 27406346-12 2016 Among patients with HER2-positive, hormone-receptor-negative cancer, the mean estimated rate of pathological complete response was 56% (95% Bayesian probability interval [PI], 37 to 73%) among 115 patients in the neratinib group, as compared with 33% among 78 controls (95% PI, 11 to 54%). neratinib 213-222 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-51 27406346-14 2016 CONCLUSIONS: Neratinib added to standard therapy was highly likely to result in higher rates of pathological complete response than standard chemotherapy with trastuzumab among patients with HER2-positive, hormone-receptor-negative breast cancer. neratinib 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 206-222 27012810-1 2016 Tamoxifen may require metabolic activation to endoxifen for efficacy in treating hormone receptor-positive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 27012810-1 2016 Tamoxifen may require metabolic activation to endoxifen for efficacy in treating hormone receptor-positive breast cancer. 4-hydroxy-N-desmethyltamoxifen 46-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 27264120-1 2016 BACKGROUND: Treatment with an aromatase inhibitor for 5 years as up-front monotherapy or after tamoxifen therapy is the treatment of choice for hormone-receptor-positive early breast cancer in postmenopausal women. Tamoxifen 95-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-160 27128111-2 2016 A recent metabolomics study identified unsaturated fatty acids, including arachidonic acid and docosahexaenoic acid (DHA), that interact with the ligand-binding domain (LBD) of a related orphan receptor, Nur77/NR4A1. Fatty Acids, Unsaturated 39-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 204-209 27128111-2 2016 A recent metabolomics study identified unsaturated fatty acids, including arachidonic acid and docosahexaenoic acid (DHA), that interact with the ligand-binding domain (LBD) of a related orphan receptor, Nur77/NR4A1. Fatty Acids, Unsaturated 39-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 210-215 27128111-2 2016 A recent metabolomics study identified unsaturated fatty acids, including arachidonic acid and docosahexaenoic acid (DHA), that interact with the ligand-binding domain (LBD) of a related orphan receptor, Nur77/NR4A1. Arachidonic Acid 74-90 nuclear receptor subfamily 4 group A member 1 Homo sapiens 204-209 27128111-2 2016 A recent metabolomics study identified unsaturated fatty acids, including arachidonic acid and docosahexaenoic acid (DHA), that interact with the ligand-binding domain (LBD) of a related orphan receptor, Nur77/NR4A1. Arachidonic Acid 74-90 nuclear receptor subfamily 4 group A member 1 Homo sapiens 210-215 27128111-2 2016 A recent metabolomics study identified unsaturated fatty acids, including arachidonic acid and docosahexaenoic acid (DHA), that interact with the ligand-binding domain (LBD) of a related orphan receptor, Nur77/NR4A1. Docosahexaenoic Acids 95-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 204-209 27128111-2 2016 A recent metabolomics study identified unsaturated fatty acids, including arachidonic acid and docosahexaenoic acid (DHA), that interact with the ligand-binding domain (LBD) of a related orphan receptor, Nur77/NR4A1. Docosahexaenoic Acids 95-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 210-215 27128111-2 2016 A recent metabolomics study identified unsaturated fatty acids, including arachidonic acid and docosahexaenoic acid (DHA), that interact with the ligand-binding domain (LBD) of a related orphan receptor, Nur77/NR4A1. Docosahexaenoic Acids 117-120 nuclear receptor subfamily 4 group A member 1 Homo sapiens 204-209 27128111-2 2016 A recent metabolomics study identified unsaturated fatty acids, including arachidonic acid and docosahexaenoic acid (DHA), that interact with the ligand-binding domain (LBD) of a related orphan receptor, Nur77/NR4A1. Docosahexaenoic Acids 117-120 nuclear receptor subfamily 4 group A member 1 Homo sapiens 210-215 27129202-5 2016 Nur77 binds adjacent to the BH3 peptide-binding crevice, suggesting the possibility of cross-talk between these discrete binding sites. BH 3 28-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 27322146-9 2016 Importantly, ATA therapy may be useful for decreasing blood glucose levels by reversing NR4A1-dependent insulin signaling. Glucose 60-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-93 27445490-1 2016 BACKGROUND: Everolimus, an inhibitor of the mammalian target of rapamycin, shows promising antitumor activity when combined with trastuzumab and chemotherapy for human epidermal growth factor receptor-2 (HER2)-positive breast cancer or when combined with endocrine agents for hormone receptor (HR)-positive tumors. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 276-292 27445490-1 2016 BACKGROUND: Everolimus, an inhibitor of the mammalian target of rapamycin, shows promising antitumor activity when combined with trastuzumab and chemotherapy for human epidermal growth factor receptor-2 (HER2)-positive breast cancer or when combined with endocrine agents for hormone receptor (HR)-positive tumors. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 294-296 27029704-1 2016 BACKGROUND: In the PALOMA-3 study, palbociclib plus fulvestrant demonstrated improved progression-free survival compared with fulvestrant plus placebo in hormone receptor-positive, HER2- endocrine-resistant metastatic breast cancer (MBC). Fulvestrant 52-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-170 27243969-2 2016 The studied flavin compounds were disubstituted with polar substituents at the N1 and N3 positions (alloxazine) or at the N3 and N10 positions (isoalloxazines). 4,6-dinitro-o-cresol 12-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 129-132 28247605-10 2016 Conclusion: Patients with HR altered from positive to negative after NAC may still gain benefit from AET. nac 69-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 26-28 27228187-0 2016 Contribution of Estrone Sulfate to Cell Proliferation in Aromatase Inhibitor (AI) -Resistant, Hormone Receptor-Positive Breast Cancer. estrone sulfate 16-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-110 26859101-1 2016 AIMS: In the SWOG S0226 trial the combination of anastrozole plus fulvestrant (n = 349) was superior to anastrozole alone (n = 345) in hormone receptor (HR)-positive metastatic breast cancer. Anastrozole 49-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 135-151 26859101-1 2016 AIMS: In the SWOG S0226 trial the combination of anastrozole plus fulvestrant (n = 349) was superior to anastrozole alone (n = 345) in hormone receptor (HR)-positive metastatic breast cancer. Anastrozole 49-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-155 26859101-1 2016 AIMS: In the SWOG S0226 trial the combination of anastrozole plus fulvestrant (n = 349) was superior to anastrozole alone (n = 345) in hormone receptor (HR)-positive metastatic breast cancer. Fulvestrant 66-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 135-151 26859101-1 2016 AIMS: In the SWOG S0226 trial the combination of anastrozole plus fulvestrant (n = 349) was superior to anastrozole alone (n = 345) in hormone receptor (HR)-positive metastatic breast cancer. Fulvestrant 66-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-155 26482374-7 2016 RESULTS: We found a positive correlation between the variant GG genotype of CTSO rs10030044 and shorter disease-free survival, or overall survival in hormone receptor-positive breast cancer patients receiving adjuvant tamoxifen therapy. Tamoxifen 218-227 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-166 26482374-9 2016 Multivariate Cox regression analysis revealed that this genotype was an independent factor indicating a poor prognosis in hormone receptor-positive breast cancer patients receiving adjuvant tamoxifen therapy. Tamoxifen 190-199 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-138 28247605-9 2016 Cox regression analysis showed that AET-administered or not was the independent predictor for 5-year DFS (HR=2.096, 95% CI:1.081-4.065, P<0.05). 2-(2-Aminoethyl)isothiourea dihydrobromide 36-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-108 28247605-10 2016 Conclusion: Patients with HR altered from positive to negative after NAC may still gain benefit from AET. 2-(2-Aminoethyl)isothiourea dihydrobromide 101-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 26-28 27313785-0 2016 Effects of CDK4/6 Inhibition in Hormone Receptor-Positive/Human Epidermal Growth Factor Receptor 2-Negative Breast Cancer Cells with Acquired Resistance to Paclitaxel. Paclitaxel 156-166 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-48 27144436-5 2016 1,1-Bis(3-indolyl)-1-(p-substituted phenyl)methane (C-DIM) analogs containing p-hydroxyl (DIM-C-pPhOH) and p-carboxymethyl (DIM-C-pPhCO2Me) substituents are NR4A1 ligands that decreased NR4A1-dependent transactivation in RMS cells and inhibited RMS cell and tumor growth and induced apoptosis. 1,1-bis(3-indolyl)-1-(p-substituted phenyl)methane 0-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-162 27144436-5 2016 1,1-Bis(3-indolyl)-1-(p-substituted phenyl)methane (C-DIM) analogs containing p-hydroxyl (DIM-C-pPhOH) and p-carboxymethyl (DIM-C-pPhCO2Me) substituents are NR4A1 ligands that decreased NR4A1-dependent transactivation in RMS cells and inhibited RMS cell and tumor growth and induced apoptosis. 1,1-bis(3-indolyl)-1-(p-substituted phenyl)methane 0-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 186-191 27144436-5 2016 1,1-Bis(3-indolyl)-1-(p-substituted phenyl)methane (C-DIM) analogs containing p-hydroxyl (DIM-C-pPhOH) and p-carboxymethyl (DIM-C-pPhCO2Me) substituents are NR4A1 ligands that decreased NR4A1-dependent transactivation in RMS cells and inhibited RMS cell and tumor growth and induced apoptosis. c-dim 52-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-162 27144436-5 2016 1,1-Bis(3-indolyl)-1-(p-substituted phenyl)methane (C-DIM) analogs containing p-hydroxyl (DIM-C-pPhOH) and p-carboxymethyl (DIM-C-pPhCO2Me) substituents are NR4A1 ligands that decreased NR4A1-dependent transactivation in RMS cells and inhibited RMS cell and tumor growth and induced apoptosis. c-dim 52-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 186-191 27144436-7 2016 Both NR4A1 knockdown and treatment with DIM-C-pPhOH and DIM-C-pPhCO2Me also induced ROS which activated stress genes and induced sestrin 2 which activated AMPK and inhibited mTOR in the mutant p53 RMS cells. p-carboxymethylphenyl 1,1-bis(3'-indolyl)-1-(p-carboxymethylphenyl)methane 56-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 5-10 27144436-7 2016 Both NR4A1 knockdown and treatment with DIM-C-pPhOH and DIM-C-pPhCO2Me also induced ROS which activated stress genes and induced sestrin 2 which activated AMPK and inhibited mTOR in the mutant p53 RMS cells. ros 84-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 5-10 27313785-3 2016 Although CDK4/6 inhibition by palbociclib in combination with endocrine therapy has shown potent antiproliferative effects in HR-positive/human epidermal growth factor receptor 2 (HER2)-negative breast cancer, the potential role of palbociclib in re-sensitizing chemotherapy-resistant HR-positive breast cancer is not well defined. palbociclib 30-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-128 27313785-4 2016 We hypothesized that CDK4/6 inhibition by palbociclib re-sensitizes HR-positive/HER2-negative residual breast cancer to taxane-based adjuvant therapy. palbociclib 42-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-70 27313785-4 2016 We hypothesized that CDK4/6 inhibition by palbociclib re-sensitizes HR-positive/HER2-negative residual breast cancer to taxane-based adjuvant therapy. taxane 120-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-70 27313785-9 2016 Nevertheless, the fact that CDK4/6 activation remained intact in paclitaxel-resistant cells indicates that patients who have HR-positive/HER2-negative residual disease after taxane-based neoadjuvant chemotherapy may still benefit from palbociclib in combination with other regimens, such as endocrine therapies, for adjuvant therapy. Paclitaxel 65-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-127 27182557-7 2016 Tumor uptake of the radiotracer 18F-fluorodeoxyglucose was associated with protein expression clusters characterized by hormone receptor loss, PTEN alteration, and HER2 gene amplification. Fluorodeoxyglucose F18 32-54 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-136 27123064-12 2016 The present study demonstrated that neoadjuvant FEC followed by weekly administration of paclitaxel and/or trastuzumab induces a high pathological response and a high pCR rate in patients with hormone receptor-negative breast cancer. Paclitaxel 89-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 193-209 27123064-0 2016 Pathological complete response rate in hormone receptor-negative breast cancer treated with neoadjuvant FEC, followed by weekly paclitaxel administration: A retrospective study and review of the literature. Paclitaxel 128-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-55 26947331-0 2016 Fulvestrant plus palbociclib versus fulvestrant plus placebo for treatment of hormone-receptor-positive, HER2-negative metastatic breast cancer that progressed on previous endocrine therapy (PALOMA-3): final analysis of the multicentre, double-blind, phase 3 randomised controlled trial. Fulvestrant 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-94 25900861-0 2016 Identification of patients with hormone receptor-positive breast cancer who need adjuvant tamoxifen therapy for more than 5 years. Tamoxifen 90-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-48 25900861-1 2016 BACKGROUND/PURPOSE: Extended hormonal therapy with tamoxifen for > 5 years has improved disease-free survival (DFS) and overall survival (OS) in hormone receptor (HR)-positive breast cancer patients. Tamoxifen 51-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 148-164 25900861-1 2016 BACKGROUND/PURPOSE: Extended hormonal therapy with tamoxifen for > 5 years has improved disease-free survival (DFS) and overall survival (OS) in hormone receptor (HR)-positive breast cancer patients. Tamoxifen 51-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-168 25900861-10 2016 CONCLUSION: Our findings suggest that HR-positive breast cancer women either aged < 40 years or with positive lymph node status were justified in continuing with tamoxifen therapy for > 5 years. Tamoxifen 165-174 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-40 26947172-1 2016 PURPOSE: This review compared the real-world effectiveness of everolimus-based therapy versus endocrine monotherapy or chemotherapy in postmenopausal hormone receptor positive (HR+)/ human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer (mBC) patients with multiple metastatic sites. Everolimus 62-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-166 26152740-1 2016 PURPOSE: Most hormone receptor (HR)(+)/HER2(-) breast cancer patients respond unfavorably to neoadjuvant chemotherapy (NAC); however, genomic tests may identify those patients who are likely to benefit. nac 119-122 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-30 26984766-1 2016 BACKGROUND: Neoadjuvant endocrine therapy (NAE) has been employed to improve surgical outcomes for hormone receptor-positive breast cancers in postmenopausal women. N-lauroylethanolamine 43-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-115 26311476-5 2016 DISCUSSION: In light of the potential for environmental release of oil and gas chemicals that can disrupt hormone receptor systems, we recommend methods for assessing complex hormonally active environmental mixtures. Oils 67-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-122 26829011-5 2016 Hormone receptor negative (HR-) patients on lapatinib had a significantly prolonged disease-free survival (DFS) compared to HR- patients on placebo (hazard ratio 0.64, P=0.003). Lapatinib 44-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 26440050-5 2016 Here, we clone and express the novel TR3-iso2 protein and find that expression of TR3-iso2, in contrast to TR3-iso1, inhibits endothelial cell proliferation induced by VEGF-A, histamine, and phorbol-12-myristate-13-acetate (PMA). Histamine 176-185 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-40 26440050-5 2016 Here, we clone and express the novel TR3-iso2 protein and find that expression of TR3-iso2, in contrast to TR3-iso1, inhibits endothelial cell proliferation induced by VEGF-A, histamine, and phorbol-12-myristate-13-acetate (PMA). Histamine 176-185 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-85 26440050-5 2016 Here, we clone and express the novel TR3-iso2 protein and find that expression of TR3-iso2, in contrast to TR3-iso1, inhibits endothelial cell proliferation induced by VEGF-A, histamine, and phorbol-12-myristate-13-acetate (PMA). Histamine 176-185 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-85 26440050-5 2016 Here, we clone and express the novel TR3-iso2 protein and find that expression of TR3-iso2, in contrast to TR3-iso1, inhibits endothelial cell proliferation induced by VEGF-A, histamine, and phorbol-12-myristate-13-acetate (PMA). Tetradecanoylphorbol Acetate 191-222 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-40 26440050-5 2016 Here, we clone and express the novel TR3-iso2 protein and find that expression of TR3-iso2, in contrast to TR3-iso1, inhibits endothelial cell proliferation induced by VEGF-A, histamine, and phorbol-12-myristate-13-acetate (PMA). Tetradecanoylphorbol Acetate 191-222 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-85 26440050-5 2016 Here, we clone and express the novel TR3-iso2 protein and find that expression of TR3-iso2, in contrast to TR3-iso1, inhibits endothelial cell proliferation induced by VEGF-A, histamine, and phorbol-12-myristate-13-acetate (PMA). Tetradecanoylphorbol Acetate 191-222 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-85 26440050-8 2016 We further demonstrate that several intracellular signaling pathways are involved in histamine-induced TR3 transcript variants, including histamine receptor H1-mediated phospholipase C (PLC)/calcium /calcineurin/protein kinase C (PKC)/protein kinase D (PKD) pathway and ERK pathway, as well as histamine receptor H3-mediated PKC-ERK pathway. Histamine 85-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-106 26440050-9 2016 Further, expressions of TR3-TV1, TR3-TV2, and TR3-TV3 by VEGF and histamine are regulated by different promoters, but not by their mRNA stability. Histamine 66-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 24-27 26440050-9 2016 Further, expressions of TR3-TV1, TR3-TV2, and TR3-TV3 by VEGF and histamine are regulated by different promoters, but not by their mRNA stability. Histamine 66-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-36 26440050-9 2016 Further, expressions of TR3-TV1, TR3-TV2, and TR3-TV3 by VEGF and histamine are regulated by different promoters, but not by their mRNA stability. Histamine 66-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-36 26354331-5 2016 In DETECT IVa, postmenopausal patients with hormone-receptor positive primary cancer and HER2-negative CTC receive everolimus and standard endocrine therapy. Everolimus 115-125 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-60 26507507-0 2016 Dosing and Safety Implications for Oncologists When Administering Everolimus to Patients With Hormone Receptor-Positive Breast Cancer. Everolimus 66-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-110 26507507-2 2016 Because of the significant improvement in progression-free survival for everolimus plus exemestane compared with exemestane plus placebo, everolimus, an mTOR inhibitor, was approved in the United States for the treatment of patients with hormone receptor-positive (HR+), HER-negative, advanced breast cancer whose disease had progressed while receiving letrozole or anastrozole. Everolimus 138-148 nuclear receptor subfamily 4 group A member 1 Homo sapiens 238-254 26786154-3 2016 Of the 12,198 women with hormone receptor-positive breast cancer, 74.8 % received AET within 12 months of diagnosis, of which 17.3 % received tamoxifen and 82.8 % received AIs. 2-(2-Aminoethyl)isothiourea dihydrobromide 82-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-41 26505879-0 2016 Honokiol sensitizes breast cancer cells to TNF-alpha induction of apoptosis by inhibiting Nur77 expression. honokiol 0-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-95 26876074-7 2016 CONCLUSION: Tumor-infiltrating lymphocytes-positive and HR-negative were independent predictive factors of pCR in primary HER2-positive breast cancer treated with trastuzumab-based NAC. nac 181-184 nuclear receptor subfamily 4 group A member 1 Homo sapiens 56-58 26505879-9 2016 Our in vitro and animal studies also identified honokiol as an effective sensitizer of TNF-alpha-induced apoptosis by inhibiting TNF-alpha-induced Nur77 mRNA expression, which could be attributed to its interference of TNFR1"s interaction with receptor-interacting protein 1 (RIPK1). honokiol 48-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 147-152 26707825-6 2016 The treated keratinocytes show a dose-dependent growth reduction to DHT and T. DHT increases the expression of TR3 in keratinocytes, associated with a concomitant increase of BAD and decrease of Bcl-2 expression. Dihydrotestosterone 79-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-114 26613834-4 2016 The administration of an aromatase inhibitor plus OFS represents an additional therapeutic option for hormone-receptor positive premenopausal breast cancer patients, according to the combined analysis of the SOFT and TEXT trials. ofs 50-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-118 26707825-7 2016 Knockdown TR3 expression by siRNA blocks the inhibitory effect of DHT on keratinocyte proliferation. Dihydrotestosterone 66-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-13 26779371-3 2015 Everolimus, an mTOR inhibitor, is currently approved for the treatment of hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-90 26779371-3 2015 Everolimus, an mTOR inhibitor, is currently approved for the treatment of hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-94 26315555-9 2015 Further subgroup analyses showed that aspirin use could decrease risk of in situ breast tumors or hormone receptor-positive tumors and reduce risk of breast cancer in postmenopausal women. Aspirin 38-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 98-114 26396259-7 2015 Both total cholesterol and low-density lipoprotein cholesterol levels in plasma were positively correlated with NR4A1 mRNA level. Cholesterol 11-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-117 26396259-10 2015 Supporting our clinical observations, cholesterol enhanced p300 acetyltransferase and decreased HDAC7 (histone deacetylase 7) recruitment to the NR4A1 promoter region, resulting in histone H3 hyperacetylation and further contributing to NR4A1 up-regulation in monocytes. Cholesterol 38-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-150 26396259-10 2015 Supporting our clinical observations, cholesterol enhanced p300 acetyltransferase and decreased HDAC7 (histone deacetylase 7) recruitment to the NR4A1 promoter region, resulting in histone H3 hyperacetylation and further contributing to NR4A1 up-regulation in monocytes. Cholesterol 38-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-242 26396259-11 2015 Moreover, cytosporone B, an NR4A1 agonist, completely reversed cholesterol-induced IL-6 (interleukin 6) and MCP-1 (monocyte chemoattractant protein 1) expression to below basal levels, and knockdown of NR4A1 expression by siRNA not only mimicked, but also exaggerated the effects of cholesterol on inflammatory biomarker up-regulation. cytosporone B 10-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 26396259-11 2015 Moreover, cytosporone B, an NR4A1 agonist, completely reversed cholesterol-induced IL-6 (interleukin 6) and MCP-1 (monocyte chemoattractant protein 1) expression to below basal levels, and knockdown of NR4A1 expression by siRNA not only mimicked, but also exaggerated the effects of cholesterol on inflammatory biomarker up-regulation. cytosporone B 10-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 202-207 26396259-11 2015 Moreover, cytosporone B, an NR4A1 agonist, completely reversed cholesterol-induced IL-6 (interleukin 6) and MCP-1 (monocyte chemoattractant protein 1) expression to below basal levels, and knockdown of NR4A1 expression by siRNA not only mimicked, but also exaggerated the effects of cholesterol on inflammatory biomarker up-regulation. Cholesterol 63-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 26396259-11 2015 Moreover, cytosporone B, an NR4A1 agonist, completely reversed cholesterol-induced IL-6 (interleukin 6) and MCP-1 (monocyte chemoattractant protein 1) expression to below basal levels, and knockdown of NR4A1 expression by siRNA not only mimicked, but also exaggerated the effects of cholesterol on inflammatory biomarker up-regulation. Cholesterol 63-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 202-207 26556724-8 2015 Our findings showed that ApoA-IV colocalizes with NR4A1, which suppresses G6Pase and PEPCK gene expression at the transcriptional level, reducing hepatic glucose output and lowering blood glucose. Glucose 154-161 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-55 26324355-1 2015 OBJECTIVE: To review palbociclib, a novel small-molecule inhibitor of cyclin-dependent kinases 4 and 6, and its current place in therapy for the treatment of hormone receptor (HMR)-positive, human epidermal growth factor receptor 2 (Her2)-negative advanced breast cancer. palbociclib 21-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 158-174 26324355-1 2015 OBJECTIVE: To review palbociclib, a novel small-molecule inhibitor of cyclin-dependent kinases 4 and 6, and its current place in therapy for the treatment of hormone receptor (HMR)-positive, human epidermal growth factor receptor 2 (Her2)-negative advanced breast cancer. palbociclib 21-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 176-179 26315555-10 2015 Aspirin use may not affect overall risk of breast cancer, but decrease risk of in situ breast tumors or hormone receptor-positive tumors and reduce risk of breast cancer in postmenopausal women. Aspirin 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 26229035-7 2015 1,1-Bis(3"-indolyl)-1-(p-substituted phenyl)methanes (C-DIMs) are NR4A1 ligands that act as NR4A1 antagonists. c-dims 54-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-97 26491966-2 2015 In this study, we investigated the anti-proliferative effect of quercetin in two breast cancer cell lines (MCF-7 and MDA-MB-231), which differed in hormone receptor. Quercetin 64-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 148-164 25677034-11 2015 Overall, our results confirm the association between alcohol intake and both hormone receptor positive and hormone receptor negative breast tumors, suggesting that timing of exposure to alcohol drinking may affect the risk. Alcohols 53-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-93 25677034-11 2015 Overall, our results confirm the association between alcohol intake and both hormone receptor positive and hormone receptor negative breast tumors, suggesting that timing of exposure to alcohol drinking may affect the risk. Alcohols 53-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-123 25677034-11 2015 Overall, our results confirm the association between alcohol intake and both hormone receptor positive and hormone receptor negative breast tumors, suggesting that timing of exposure to alcohol drinking may affect the risk. Alcohols 186-193 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-93 25677034-11 2015 Overall, our results confirm the association between alcohol intake and both hormone receptor positive and hormone receptor negative breast tumors, suggesting that timing of exposure to alcohol drinking may affect the risk. Alcohols 186-193 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-123 26362840-0 2015 Intermittent Letrozole Administration as Adjuvant Endocrine Therapy for Postmenopausal Women With Hormone Receptor-Positive Early Breast Cancer: A Biologic Study. Letrozole 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 98-114 26446233-7 2015 Subgroup analysis revealed that metformin improved the overall survival by 65% after adjusting for hormone receptor expression (HR: 0.35; 95% CI: 0.15-0.84). Metformin 32-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-115 26446233-12 2015 Subgroup analysis revealed that metformin improved the overall survival by 65% after adjusting for hormone receptor expression. Metformin 32-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-115 26392314-9 2015 These results suggest that HCV core protein decreases the sensitivity of hepatocytes to cisplatin by inhibiting the expression of NR4A1 and promoting the expression of smad7, which negatively regulates the TGF-beta pathway. Cisplatin 88-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 130-135 26229035-7 2015 1,1-Bis(3"-indolyl)-1-(p-substituted phenyl)methanes (C-DIMs) are NR4A1 ligands that act as NR4A1 antagonists. 1,1-bis(3"-indolyl)-1-(p-substituted phenyl)methanes 0-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-71 26229035-7 2015 1,1-Bis(3"-indolyl)-1-(p-substituted phenyl)methanes (C-DIMs) are NR4A1 ligands that act as NR4A1 antagonists. 1,1-bis(3"-indolyl)-1-(p-substituted phenyl)methanes 0-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-97 26417203-2 2015 Several clinical trials have shown that the mTOR inhibitor everolimus could improve patient outcomes in several subtypes of breast cancer, including hormone receptor-positive, human epidermal growth factor receptor-negative metastatic disease that has progressed after prior endocrine therapy. Everolimus 59-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-165 26229035-7 2015 1,1-Bis(3"-indolyl)-1-(p-substituted phenyl)methanes (C-DIMs) are NR4A1 ligands that act as NR4A1 antagonists. c-dims 54-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-71 26148973-8 2015 In particular, SR11237 (BMS649) has stronger potency for recruitment of CoA motif and transcriptional activity with the heterodimer Nur77/RXR than other complexes. SR 11237 15-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-137 26148973-8 2015 In particular, SR11237 (BMS649) has stronger potency for recruitment of CoA motif and transcriptional activity with the heterodimer Nur77/RXR than other complexes. BMS 649 24-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-137 26417636-1 2015 Two randomised trials have compared 5 years versus 10 years of tamoxifen therapy following surgery for hormone receptor-positive early breast cancer. Tamoxifen 63-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-119 26264704-1 2015 Palbociclib was approved by the FDA for use in combination with letrozole for the treatment of postmenopausal women with hormone-receptor-positive, HER2-negative advanced breast cancer as initial endocrine-based therapy. palbociclib 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-137 26235054-3 2015 We previously reported that autophagic cell death mediated by nuclear receptor TR3 and driven by a chemical agonist, 1-(3,4,5-trihydroxyphenyl)nonan-1-one (THPN), is highly effective in the therapy of melanoma but not any other cancer types. 1-(3,4,5-trihydroxyphenyl)nonan-1-one 156-160 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-82 25703176-0 2015 Mixture effects of levonorgestrel and ethinylestradiol: estrogenic biomarkers and hormone receptor mRNA expression during sexual programming. Levonorgestrel 19-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-98 25624176-3 2015 In the last years many targeted agents have been investigated to prevent or overcome endocrine resistance; only a few of them have been found effective in HR positive MBC, such as everolimus, CK4/6 inhibitors and HDAC inhibitors. Everolimus 180-190 nuclear receptor subfamily 4 group A member 1 Homo sapiens 155-157 26270486-2 2015 A NR4A1/bis-indole ligand complex at this novel site has been found to be stable over 1 mus of simulation and to result in an interesting conformational transmission to a remote loop that has the capacity to communicate with a NBRE within a RXR-alpha/NR4A1 heterodimer. Bismuth 8-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 2-7 26270486-2 2015 A NR4A1/bis-indole ligand complex at this novel site has been found to be stable over 1 mus of simulation and to result in an interesting conformational transmission to a remote loop that has the capacity to communicate with a NBRE within a RXR-alpha/NR4A1 heterodimer. Bismuth 8-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 251-256 26270486-2 2015 A NR4A1/bis-indole ligand complex at this novel site has been found to be stable over 1 mus of simulation and to result in an interesting conformational transmission to a remote loop that has the capacity to communicate with a NBRE within a RXR-alpha/NR4A1 heterodimer. indole 12-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 2-7 26270486-2 2015 A NR4A1/bis-indole ligand complex at this novel site has been found to be stable over 1 mus of simulation and to result in an interesting conformational transmission to a remote loop that has the capacity to communicate with a NBRE within a RXR-alpha/NR4A1 heterodimer. indole 12-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 251-256 26035713-5 2015 We have recently demonstrated that selected 1,1-bis(3"-indolyl)-1-(p-substituted phenyl)methane (C-DIM) compounds including the p-hydroxyphenyl (DIM-C-pPhOH) and p-carboxymethyl (DIM-C-pPhCO2Me) analogs bind NR4A1 and act as antagonists. 1,1-bis(3"-indolyl)-1-(p-substituted phenyl)methane 44-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 26035713-5 2015 We have recently demonstrated that selected 1,1-bis(3"-indolyl)-1-(p-substituted phenyl)methane (C-DIM) compounds including the p-hydroxyphenyl (DIM-C-pPhOH) and p-carboxymethyl (DIM-C-pPhCO2Me) analogs bind NR4A1 and act as antagonists. c-dim 97-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 26035713-5 2015 We have recently demonstrated that selected 1,1-bis(3"-indolyl)-1-(p-substituted phenyl)methane (C-DIM) compounds including the p-hydroxyphenyl (DIM-C-pPhOH) and p-carboxymethyl (DIM-C-pPhCO2Me) analogs bind NR4A1 and act as antagonists. p-hydroxyphenyl 128-143 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 25792492-1 2015 UNLABELLED: In postmenopausal women with low bone mass and hormone-receptor-positive breast cancer on an aromatase inhibitor, risedronate maintained skeletal health assessed by bone density and turnover markers. Risedronic Acid 126-137 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-75 26102468-3 2015 In March 2007, lapatinib, an oral dual-tyrosine kinase inhibitor was approved in combination with capecitabine for metastatic HER-2-positive breast cancer that has progressed on prior trastuzumab therapy, and in combination with letrozole for postmenopausal women with HER-2 and hormone receptor-positive advanced breast cancer. Lapatinib 15-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 279-295 25760782-9 2015 However, elevated risks for hormone receptor-negative tumors were observed for higher exposure to cadmium compounds and possibly inorganic arsenic among never-smoking non-movers. Cadmium 98-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-44 25760782-9 2015 However, elevated risks for hormone receptor-negative tumors were observed for higher exposure to cadmium compounds and possibly inorganic arsenic among never-smoking non-movers. Arsenic 139-146 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-44 25703176-0 2015 Mixture effects of levonorgestrel and ethinylestradiol: estrogenic biomarkers and hormone receptor mRNA expression during sexual programming. Ethinyl Estradiol 38-54 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-98 25663912-6 2015 Compared with the patients who did not receive lapatinib, the pCR rate was higher in the hormone receptor (HR)-positive [risk ratio (RR), 1.39; 95% confidence interval (CI), 1.12-1.72; P=0.002) and HR-negative (RR, 1.38; 95% CI, 1.14-1.68; P=0.0009) patients that received lapatinib. Lapatinib 47-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-105 25931227-2 2015 METHODS: The fusion protein PET28a-NR4A1-DBD was constructed and purified with the nickel affinity chromatography, cation-exchange chromatography and gel filtration chromatography. Nickel 83-89 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-40 25931227-3 2015 RESULTS: The protein PET28a-NR4A1-DBD was mostly soluable at 24 C. A total of 2-3 mg/L pure NR4A1 proteins were yielded in bacterial culture and the purity for final fractions of NR4A1-DBD protein were great than 95% by SDS-PAGE analysis. Sodium Dodecyl Sulfate 221-224 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 25931227-3 2015 RESULTS: The protein PET28a-NR4A1-DBD was mostly soluable at 24 C. A total of 2-3 mg/L pure NR4A1 proteins were yielded in bacterial culture and the purity for final fractions of NR4A1-DBD protein were great than 95% by SDS-PAGE analysis. Sodium Dodecyl Sulfate 221-224 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-98 25931227-3 2015 RESULTS: The protein PET28a-NR4A1-DBD was mostly soluable at 24 C. A total of 2-3 mg/L pure NR4A1 proteins were yielded in bacterial culture and the purity for final fractions of NR4A1-DBD protein were great than 95% by SDS-PAGE analysis. Sodium Dodecyl Sulfate 221-224 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-98 25663912-6 2015 Compared with the patients who did not receive lapatinib, the pCR rate was higher in the hormone receptor (HR)-positive [risk ratio (RR), 1.39; 95% confidence interval (CI), 1.12-1.72; P=0.002) and HR-negative (RR, 1.38; 95% CI, 1.14-1.68; P=0.0009) patients that received lapatinib. Lapatinib 47-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-109 25663912-6 2015 Compared with the patients who did not receive lapatinib, the pCR rate was higher in the hormone receptor (HR)-positive [risk ratio (RR), 1.39; 95% confidence interval (CI), 1.12-1.72; P=0.002) and HR-negative (RR, 1.38; 95% CI, 1.14-1.68; P=0.0009) patients that received lapatinib. Lapatinib 273-282 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-105 25663912-6 2015 Compared with the patients who did not receive lapatinib, the pCR rate was higher in the hormone receptor (HR)-positive [risk ratio (RR), 1.39; 95% confidence interval (CI), 1.12-1.72; P=0.002) and HR-negative (RR, 1.38; 95% CI, 1.14-1.68; P=0.0009) patients that received lapatinib. Lapatinib 273-282 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-109 26075448-5 2015 Temsirolimus is approved for advanced RCC; everolimus is registered for the treatment of advanced RCC, pancreatic neuroendocrine tumors and postmenopausal, hormone receptor-positive/HER2-negative, advanced breast cancer. Everolimus 43-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 156-172 25232032-0 2015 Bile acids regulate nuclear receptor (Nur77) expression and intracellular location to control proliferation and apoptosis. Bile Acids and Salts 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 25232032-4 2015 The intracellular location of BA-induced Nur77 was time dependent; short-term (1-3 hours) exposure induced nuclear Nur77, whereas longer (1-2 days) exposure also increased cytosolic Nur77 expression and apoptosis. Bile Acids and Salts 30-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 25232032-4 2015 The intracellular location of BA-induced Nur77 was time dependent; short-term (1-3 hours) exposure induced nuclear Nur77, whereas longer (1-2 days) exposure also increased cytosolic Nur77 expression and apoptosis. Bile Acids and Salts 30-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-120 25232032-4 2015 The intracellular location of BA-induced Nur77 was time dependent; short-term (1-3 hours) exposure induced nuclear Nur77, whereas longer (1-2 days) exposure also increased cytosolic Nur77 expression and apoptosis. Bile Acids and Salts 30-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-120 25232032-5 2015 Inhibiting Nur77 nuclear export with leptomycin B decreased lithocholic acid (LCA)-induced apoptosis. leptomycin B 37-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-16 25232032-5 2015 Inhibiting Nur77 nuclear export with leptomycin B decreased lithocholic acid (LCA)-induced apoptosis. Lithocholic Acid 60-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-16 25232032-5 2015 Inhibiting Nur77 nuclear export with leptomycin B decreased lithocholic acid (LCA)-induced apoptosis. Lithocholic Acid 78-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-16 25232032-6 2015 Extended (7 days) treatment with BA generated resistance to BA with increased nuclear Nur77, viability, and mobility. Bile Acids and Salts 33-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-91 25232032-7 2015 While, knockdown of Nur77 in BA-resistant cells increased cellular susceptibility to LCA-induced apoptosis. Lithocholic Acid 85-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-25 25232032-10 2015 Consistently, BA-induced upregulation of the aforementioned genes was abrogated by a lack of Nur77. Bile Acids and Salts 14-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-98 25232032-11 2015 Importantly, Nur77 was overexpressed in high percentage of human colon and liver cancer specimens, and the intracellular location of Nur77 correlated with elevated serum total BA levels in patients with colon cancer. Bile Acids and Salts 176-178 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 25232032-11 2015 Importantly, Nur77 was overexpressed in high percentage of human colon and liver cancer specimens, and the intracellular location of Nur77 correlated with elevated serum total BA levels in patients with colon cancer. Bile Acids and Salts 176-178 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-138 25330024-0 2015 Nuclear receptor subfamily 4, group A, member 1 inhibits extrinsic apoptosis and reduces caspase-8 activity in H2O2-induced human HUC-F2 fibroblasts. Hydrogen Peroxide 111-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-47 25330024-4 2015 In the current study, we focused on the potential role of NR4A1 in hydrogen peroxide (H2O2)-induced apoptosis of normal human umbilical cord fibroblast (HUC-F2) cells. Hydrogen Peroxide 67-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-63 25330024-4 2015 In the current study, we focused on the potential role of NR4A1 in hydrogen peroxide (H2O2)-induced apoptosis of normal human umbilical cord fibroblast (HUC-F2) cells. Hydrogen Peroxide 86-90 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-63 25330024-10 2015 RESULTS: H2O2 treatment led to enhanced NR4A1 expression. Hydrogen Peroxide 9-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-45 25488719-6 2015 An interaction between HER2 and HR was observed, with a HER2-positive status significantly associated with ALN involvement at the time of diagnosis only in HR-negative patients (P < 0.0001). aln 107-110 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-34 25488719-8 2015 The HR and HER2 statuses are significantly associated with ALN involvement at the time of diagnosis. aln 59-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-6 26273337-8 2015 NAC can alter HR and Ki-67 status in breast adenocarcinoma patients. nac 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-16 26457979-1 2015 BACKGROUND: Everolimus (Afinitor ) plus exemestane are indicated for hormone receptor-positive, HER2/neu-negative metastatic breast cancer (MBC), in menopausal women without symptomatic visceral disease after recurrence or progression following aromatase inhibitors. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 26457979-1 2015 BACKGROUND: Everolimus (Afinitor ) plus exemestane are indicated for hormone receptor-positive, HER2/neu-negative metastatic breast cancer (MBC), in menopausal women without symptomatic visceral disease after recurrence or progression following aromatase inhibitors. Everolimus 24-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 26457979-1 2015 BACKGROUND: Everolimus (Afinitor ) plus exemestane are indicated for hormone receptor-positive, HER2/neu-negative metastatic breast cancer (MBC), in menopausal women without symptomatic visceral disease after recurrence or progression following aromatase inhibitors. exemestane 40-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 25385240-5 2014 RESULTS: The administration of ET was significantly associated with improved disease-free survival (p=0.018) in patients with a positive-to-negative switch of HR status. et 31-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-161 25505228-1 2015 BACKGROUND: There is limited evidence on the association between dietary folate intake and the risk of breast cancer (BC) by hormone receptor expression in the tumors. Folic Acid 73-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 25505228-15 2015 CONCLUSIONS: Higher dietary folate intake may be associated with a lower risk of sex hormone receptor-negative BC in premenopausal women. Folic Acid 28-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 25385240-8 2014 CONCLUSIONS: This study revealed that patients with HR altered from positive to negative after NAC still benefit from ET. nac 95-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-54 25385240-9 2014 The HR status should be evaluated not only in specimens obtained during post-NAC surgery but also in specimens biopsied before NAC. nac 77-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-6 25385240-9 2014 The HR status should be evaluated not only in specimens obtained during post-NAC surgery but also in specimens biopsied before NAC. nac 127-130 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-6 25284689-3 2014 By using quantitative real-time PCR (qRT-PCR) and enzyme-linked immunosorbent assay (ELISA), we show that either ectopic expression of orphan nuclear receptor Nur77 or pharmacological activation of Nur77 by 6-mercaptopurine (6-MP) substantially inhibits ET-1 expression in human umbilical vein endothelial cells (HUVECs), under both basal and thrombin-stimulated conditions. Mercaptopurine 207-223 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-164 25451590-6 2014 Global gene expression analysis confirmed by real-time PCR revealed that shikonin drastically inhibited the IgE/antigen-induced and calcium ionophore-induced upregulation of mRNA expression of the nuclear orphan receptor 4a family (Nr4a1, Nr4a2 and Nr4a3) in mBMMCs, and knockdown of Nr4a1 or Nr4a2 suppressed the IgE/antigen-induced upregulation of TNF-alpha mRNA expression. Calcium 132-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 232-237 25451590-6 2014 Global gene expression analysis confirmed by real-time PCR revealed that shikonin drastically inhibited the IgE/antigen-induced and calcium ionophore-induced upregulation of mRNA expression of the nuclear orphan receptor 4a family (Nr4a1, Nr4a2 and Nr4a3) in mBMMCs, and knockdown of Nr4a1 or Nr4a2 suppressed the IgE/antigen-induced upregulation of TNF-alpha mRNA expression. Calcium 132-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 284-289 25187486-0 2014 Induction of Nur77-dependent apoptotic pathway by a coumarin derivative through activation of JNK and p38 MAPK. coumarin 52-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 25284689-3 2014 By using quantitative real-time PCR (qRT-PCR) and enzyme-linked immunosorbent assay (ELISA), we show that either ectopic expression of orphan nuclear receptor Nur77 or pharmacological activation of Nur77 by 6-mercaptopurine (6-MP) substantially inhibits ET-1 expression in human umbilical vein endothelial cells (HUVECs), under both basal and thrombin-stimulated conditions. Mercaptopurine 207-223 nuclear receptor subfamily 4 group A member 1 Homo sapiens 198-203 25239681-0 2014 Assessing the impact of CMF-like/Anthracycline-based/Anthracycline-Taxane-based/dose-dense chemotherapy in dependency of positive axillary lymph nodes/hormone receptor-status/grading/T-stage on survival - A retrospective multi-centre cohort study of 3677 patients receiving adjuvant chemotherapy. Anthracyclines 53-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 151-167 23404211-1 2014 BACKGROUND: The addition of mTOR inhibitor everolimus (EVE) to exemestane (EXE) was evaluated in an international, phase 3 study (BOLERO-2) in patients with hormone-receptor-positive (HR(+)) breast cancer refractory to letrozole or anastrozole. Everolimus 43-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-173 25239681-0 2014 Assessing the impact of CMF-like/Anthracycline-based/Anthracycline-Taxane-based/dose-dense chemotherapy in dependency of positive axillary lymph nodes/hormone receptor-status/grading/T-stage on survival - A retrospective multi-centre cohort study of 3677 patients receiving adjuvant chemotherapy. taxane 67-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 151-167 25471040-3 2014 The development of drugs to target these hormone receptors, such as tamoxifen, has brought about significant improvement in survival for women with hormone receptor-positive breast cancers. Tamoxifen 68-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-57 25289075-10 2014 Furthermore, 250 muM PA stimulation was shown to increase NR4A1 expression and the secretion of inflammatory cytokines in the cultured PBMCs. Palmitic Acid 21-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-63 25279188-1 2014 The aim of the present study was to investigate whether breast cancer patients with changes from positive to negative in the hormone receptor following neoadjuvant chemotherapy (NAC) could benefit from adjuvant endocrine therapy (ET). nac 178-181 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 25279188-2 2014 Between December 2000 and November 2010, 97 eligible patients with a positive-to-negative switch of the hormone receptor status following NAC were identified. nac 138-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 25279188-5 2014 The administration of ET was associated with a significantly improved disease-free survival (DFS) (P=0.018) in patients with a positive-to-negative switch of the hormone receptor status. et 22-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 162-178 25279188-8 2014 The present study revealed that patients with the hormone receptor that was altered from positive to negative following NAC benefit from ET, and the hormone receptor status should be evaluated not only in specimens obtained during post-NAC surgery, but also in specimens biopsied prior to NAC. nac 120-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-66 25279188-8 2014 The present study revealed that patients with the hormone receptor that was altered from positive to negative following NAC benefit from ET, and the hormone receptor status should be evaluated not only in specimens obtained during post-NAC surgery, but also in specimens biopsied prior to NAC. nac 236-239 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-66 25279188-8 2014 The present study revealed that patients with the hormone receptor that was altered from positive to negative following NAC benefit from ET, and the hormone receptor status should be evaluated not only in specimens obtained during post-NAC surgery, but also in specimens biopsied prior to NAC. nac 236-239 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-165 25279188-8 2014 The present study revealed that patients with the hormone receptor that was altered from positive to negative following NAC benefit from ET, and the hormone receptor status should be evaluated not only in specimens obtained during post-NAC surgery, but also in specimens biopsied prior to NAC. nac 236-239 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-66 25279188-8 2014 The present study revealed that patients with the hormone receptor that was altered from positive to negative following NAC benefit from ET, and the hormone receptor status should be evaluated not only in specimens obtained during post-NAC surgery, but also in specimens biopsied prior to NAC. nac 236-239 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-165 25090634-6 2014 The results of the in vitro study also indicated that the expression levels of 3beta-HSD1, CYP11A1, StAR, 5alpha-red1 and NGFI-B were elevated by forskolin. Colforsin 146-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-128 25275504-8 2014 The expression of HDAC1,2,3,4,7 and Nur77 increased in PA samples at levels significantly higher than those observed in the CP group (p = 0.0160; 0.0114; 0.0227; 0.0440; 0.0136; 0.0004, respectively). Protactinium 55-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 36-41 25302045-3 2014 Everolimus is an inhibitor of mtor (the mammalian target of rapamycin) that is used as targeted therapy for advanced, hormone receptor-positive, her2-negative breast cancer in postmenopausal women in combination with exemestane, after treatment failure with letrozole or anastrozole. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-134 25153259-4 2014 Testosterone-reduced expression of some steroidogenic enzymes/proteins (Tspo,StAR,Hsd3b1/2) and transcription factors (Nur77,Gata4,Dax1) was completely abrogated, while decreased expression of Star,Cyp11a1,Cyp17a1,Hsd17b4,Creb1a was partially prevented. Testosterone 0-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-124 24885573-5 2014 Glucagon and forskolin increased Nur77 and FGF21 expression in vivo and in vitro, respectively, and adenovirus-mediated overexpression of Nur77 (Ad-Nur77) increased FGF21 expression in vitro and in vivo. Glucagon 0-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-38 24840230-4 2014 METHODS: The Tamoxifen Exemestane Adjuvant Multinational Lifestyle study was a side study of the Tamoxifen Exemestane Adjuvant Multinational trial and prospectively investigated lifestyle habits of postmenopausal, hormone receptor-positive breast cancer patients. tamoxifen exemestane 13-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 214-230 25400769-13 2014 CONCLUSIONS: Our results suggest that Ki67 expression in HR-negative breast cancer may improve the assessment of pathological response after NAC, and Ki67 score in residual tumor was an independent prognosticator for DFS in the HR-negative breast cancer patients. nac 141-144 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-59 23184499-0 2014 Preoperative endocrine therapy with goserelin acetate and tamoxifen in hormone receptor-positive premenopausal breast cancer patients. Tamoxifen 58-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-87 25139196-6 2014 Among the four chemotherapy regimens, only CAX regimen had a predictive value for cOR (HR 2.30, 95 % CI 1.16-4.58, P = 0.009). CAX 43-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-89 25099012-4 2014 Moreover, we also show that knockdown of NR4A1 by RNA interference (small interfering NR4A1) or treatment with DIM-C-pPhOH and related compounds decreased colon cancer cell growth, induced apoptosis, decreased expression of survivin and other Sp-regulated genes, and inhibited mammalian target of rapamycin signaling. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 111-122 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 25063800-4 2014 We hypothesize that acute ozone (AO) exposure during postnatal airway development disrupts SP/NK-1R/Nur77 pathway expression and that these changes correlate with increased ozone-induced cell death. Acridine Orange 33-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 100-105 25063800-4 2014 We hypothesize that acute ozone (AO) exposure during postnatal airway development disrupts SP/NK-1R/Nur77 pathway expression and that these changes correlate with increased ozone-induced cell death. Ozone 26-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 100-105 25063800-8 2014 We found that 1) ozone increases SP/NK-1R/Nur77 pathway expression in conducting airways, 2) an ozone exposure cycle (5 days/cycle) delivered early at age 2 mo resulted in an airway that was hypersensitive to AO exposure at the end of 2 mo, and 3) continued episodic exposure (11 cycles) resulted in an airway that was hyposensitive to AO exposure at 6 mo. Ozone 17-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-47 25199766-9 2014 Tamoxifen is indicated for premenopausal hormone receptor (HR) positive tumors in 86.5% of cases and aromatase inhibitors (AI"s) for postmenopausal in 86%. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-57 25199766-9 2014 Tamoxifen is indicated for premenopausal hormone receptor (HR) positive tumors in 86.5% of cases and aromatase inhibitors (AI"s) for postmenopausal in 86%. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-61 24975596-10 2014 Postmenopausal women with hormone receptor-positive breast cancer receiving adjuvant anastrozole displayed less fatty liver disease, suggesting that this drug had a more favorable hepatic safety profile than tamoxifen and may be preferred for patients with potential hepatic dysfunction. Anastrozole 85-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 26-42 23837522-4 2014 The optimized formulation, NP10 was dispersed in carbopol 934 P to form nanoparticulate in situ gels (NP-ISG1--NP-ISG5). carboxypolymethylene 49-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-31 24885573-5 2014 Glucagon and forskolin increased Nur77 and FGF21 expression in vivo and in vitro, respectively, and adenovirus-mediated overexpression of Nur77 (Ad-Nur77) increased FGF21 expression in vitro and in vivo. Colforsin 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-38 24885573-6 2014 Moreover, knockdown of endogenous Nur77 expression by siRNA-Nur77 abolished the effect of forskolin on FGF21 expression. Colforsin 90-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-39 24885573-6 2014 Moreover, knockdown of endogenous Nur77 expression by siRNA-Nur77 abolished the effect of forskolin on FGF21 expression. Colforsin 90-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-65 24769509-8 2014 Moreover, we showed using salubrinal, an ER stress inhibitor that reactive oxygen species production, JNK activation, and Nur77 upregulation and its translocation to cytoplasm are necessary for ER-induced stress. salubrinal 26-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-127 25120787-1 2014 BACKGROUND: To investigate the prognostic value of hormone receptor (HR) status conversion after neoadjuvant chemotherapy (NAC) in patients with primary breast cancer. nac 123-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 24924416-0 2014 Randomised, phase II, placebo-controlled, trial of fulvestrant plus vandetanib in postmenopausal women with bone only or bone predominant, hormone-receptor-positive metastatic breast cancer (MBC): the OCOG ZAMBONEY study. vandetanib 68-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-155 25120787-5 2014 RESULTS: In total, 15.7% of patients had HR status change after NAC. nac 64-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-43 25120787-8 2014 CONCLUSIONS: The switch of HR status after NAC is remarkable for breast cancer. nac 43-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-29 24922658-6 2014 In particular, the prognostic impact of rs11614913 was limited to the hormone receptor-expressing subtype, where the patients bearing the CC genotype showed worse survival in terms of DFS and DDFS compared with the patients with the TT or TC genotype as a recessive model (hazard ratio=2.610, p=0.003 for DFS; hazard ratio=2.730, p=0.013 for DDFS). Technetium 239-241 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-86 24625784-10 2014 CONCLUSIONS: Ly-6C(high) monocytes orchestrate both inflammatory and reparative phases during myocardial infarction and depend on Nr4a1 to limit their influx and inflammatory cytokine expression. ly-6c 13-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 130-135 24751388-4 2014 Comparable visual analog scale scores for rest pain at each measured time interval among the three groups demonstrated that adequate pain relief was offered; however, the cumulative dose of nalbuphine administered to the patients in Group N10 attenuated the analgesic effect of epidural morphine in moving pain at POh24 only. Nalbuphine 190-200 nuclear receptor subfamily 4 group A member 1 Homo sapiens 239-242 24657612-1 2014 Amoitone B, a natural agonist to Nur77, is a promising anticancer drug. n-amyl 2-(3,5-dihydroxy-2-(1-nonanoyl)phenyl)acetate 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-38 24751388-4 2014 Comparable visual analog scale scores for rest pain at each measured time interval among the three groups demonstrated that adequate pain relief was offered; however, the cumulative dose of nalbuphine administered to the patients in Group N10 attenuated the analgesic effect of epidural morphine in moving pain at POh24 only. Morphine 287-295 nuclear receptor subfamily 4 group A member 1 Homo sapiens 239-242 24464780-0 2014 A phase II study of preoperative capecitabine in women with operable hormone receptor positive breast cancer. Capecitabine 33-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 24680679-0 2014 Mitochondrial translocation of Nur77 induced by ROS contributed to cardiomyocyte apoptosis in metabolic syndrome. ros 48-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-36 24680679-2 2014 Nur77, a nuclear orphan receptor, is involved in such various cellular events as apoptosis, proliferation, and glucose and lipid metabolism in several cell types. Glucose 111-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 24680679-7 2014 In this report, we observed that, accompanied by the substantial decline in apoptosis inducer Nur77, MI/R induced cardiac dysfunction was manifested as cardiomyopathy and increased ROS. r 104-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 24680679-7 2014 In this report, we observed that, accompanied by the substantial decline in apoptosis inducer Nur77, MI/R induced cardiac dysfunction was manifested as cardiomyopathy and increased ROS. ros 181-184 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 24680679-9 2014 However, inhibition of the relocation of Nur77 to mitochondria via Cyclosporin A reversed the changes in membrane potential mediated by H2O2 and reduced myocardial cell injury. Cyclosporine 67-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 24680679-9 2014 However, inhibition of the relocation of Nur77 to mitochondria via Cyclosporin A reversed the changes in membrane potential mediated by H2O2 and reduced myocardial cell injury. Hydrogen Peroxide 136-140 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 24615500-0 2014 Incidence and time course of everolimus-related adverse events in postmenopausal women with hormone receptor-positive advanced breast cancer: insights from BOLERO-2. Everolimus 29-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-108 24615500-1 2014 BACKGROUND: In the BOLERO-2 trial, everolimus (EVE), an inhibitor of mammalian target of rapamycin, demonstrated significant clinical benefit with an acceptable safety profile when administered with exemestane (EXE) in postmenopausal women with hormone receptor-positive (HR(+)) advanced breast cancer. Everolimus 35-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 245-261 24562770-4 2014 We show that the investigational drug MLN0128, which inhibits both complexes of mTOR (mTORC1 and mTORC2), and the hydroxamic acid pan-HDAC inhibitor TSA synergistically inhibit the viability of a phenotypically diverse panel of five breast cancer cell lines (HR-/+, HER2-/+). INK128 38-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 259-261 24562770-4 2014 We show that the investigational drug MLN0128, which inhibits both complexes of mTOR (mTORC1 and mTORC2), and the hydroxamic acid pan-HDAC inhibitor TSA synergistically inhibit the viability of a phenotypically diverse panel of five breast cancer cell lines (HR-/+, HER2-/+). Hydroxamic Acids 114-129 nuclear receptor subfamily 4 group A member 1 Homo sapiens 259-261 24562770-4 2014 We show that the investigational drug MLN0128, which inhibits both complexes of mTOR (mTORC1 and mTORC2), and the hydroxamic acid pan-HDAC inhibitor TSA synergistically inhibit the viability of a phenotypically diverse panel of five breast cancer cell lines (HR-/+, HER2-/+). trichostatin A 149-152 nuclear receptor subfamily 4 group A member 1 Homo sapiens 259-261 24743359-1 2014 Japanese clinical trials of a tegafur/uracil(UFT)-based postoperative chemotherapy regimen compared with cyclophosphamide, methotrexate, and fluorouracil(CMF)treatment have shown that UFT is not inferior to CMF for the treatment of hormone receptor-positive breast cancer patients. Tegafur 45-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 232-248 24743359-1 2014 Japanese clinical trials of a tegafur/uracil(UFT)-based postoperative chemotherapy regimen compared with cyclophosphamide, methotrexate, and fluorouracil(CMF)treatment have shown that UFT is not inferior to CMF for the treatment of hormone receptor-positive breast cancer patients. CMF regimen 154-157 nuclear receptor subfamily 4 group A member 1 Homo sapiens 232-248 23584473-0 2014 PKA/Smurf1 signaling-mediated stabilization of Nur77 is required for anticancer drug cisplatin-induced apoptosis. Cisplatin 85-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-52 24515801-3 2014 Treatment of pancreatic cancer cells with the NR4A1 antagonist 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) gave similar results. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 63-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-51 24515801-3 2014 Treatment of pancreatic cancer cells with the NR4A1 antagonist 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) gave similar results. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 111-122 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-51 24515801-4 2014 Moreover, both NR4A1 knockdown and DIM-C-pPhOH induced reactive oxygen species (ROS), and induction of ROS and endoplasmic reticulum stress by these agents was attenuated after cotreatment with antioxidants. Reactive Oxygen Species 55-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-20 24515801-4 2014 Moreover, both NR4A1 knockdown and DIM-C-pPhOH induced reactive oxygen species (ROS), and induction of ROS and endoplasmic reticulum stress by these agents was attenuated after cotreatment with antioxidants. Reactive Oxygen Species 80-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-20 24515801-5 2014 Manipulation of NR4A1 expression coupled with gene expression profiling identified a number of ROS metabolism transcripts regulated by NR4A1. Reactive Oxygen Species 95-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 16-21 24515801-5 2014 Manipulation of NR4A1 expression coupled with gene expression profiling identified a number of ROS metabolism transcripts regulated by NR4A1. Reactive Oxygen Species 95-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 135-140 24515801-6 2014 Knockdown of one of these transcripts, thioredoxin domain containing 5 (TXNDC5), recapitulated the elevated ROS and endoplasmic reticulum stress; thus, demonstrating that NR4A1 regulates levels of endoplasmic reticulum stress and ROS in pancreatic cancer cells to facilitate cell proliferation and survival. Reactive Oxygen Species 108-111 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-176 24515801-6 2014 Knockdown of one of these transcripts, thioredoxin domain containing 5 (TXNDC5), recapitulated the elevated ROS and endoplasmic reticulum stress; thus, demonstrating that NR4A1 regulates levels of endoplasmic reticulum stress and ROS in pancreatic cancer cells to facilitate cell proliferation and survival. Reactive Oxygen Species 230-233 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-176 24515801-7 2014 Finally, inactivation of NR4A1 by knockdown or DIM-C-pPhOH decreased TXNDC5, resulting in activation of the ROS/endoplasmic reticulum stress and proapoptotic pathways. Reactive Oxygen Species 108-111 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-30 24515801-8 2014 IMPLICATIONS: The NR4A1 receptor is pro-oncogenic, regulates the ROS/endoplasmic reticulum stress pathways, and inactivation of the receptor represents a novel pathway for inducing cell death in pancreatic cancer. Reactive Oxygen Species 65-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-23 23584473-7 2014 Accordingly, cyclic AMP/PKA signaling switches the fate of Nur77 from degradation to triggering apoptosis in chemotherapy drug cisplatin-treated cells. Cyclic AMP 13-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-64 23584473-7 2014 Accordingly, cyclic AMP/PKA signaling switches the fate of Nur77 from degradation to triggering apoptosis in chemotherapy drug cisplatin-treated cells. Cisplatin 127-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-64 23584473-8 2014 Hence, our study revealed a novel mechanism, by which PKA/Smurf1 antagonizes the downregulating effect of JNK on Nur77, leading to the accumulation of Nur77 for apoptosis induction triggered by cisplatin. Cisplatin 194-203 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-118 23584473-8 2014 Hence, our study revealed a novel mechanism, by which PKA/Smurf1 antagonizes the downregulating effect of JNK on Nur77, leading to the accumulation of Nur77 for apoptosis induction triggered by cisplatin. Cisplatin 194-203 nuclear receptor subfamily 4 group A member 1 Homo sapiens 151-156 24333837-9 2014 Taken together, telmisartan may stimulate CYP11B2 transcription via NGFIB and the CaMK-mediated induction of NURR1 that activates the Ad5 element, independent of AII type 1 receptor. Telmisartan 16-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-73 24586619-7 2014 The genome of SA268 was almost identical to that of the Taiwanese ST59 CA-MRSA strains M013 and SA957. sa268 14-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-70 24355487-1 2014 BACKGROUND: This prospective study evaluated the relationship between arthralgia and compliance during the first year of adjuvant anastrozole therapy in postmenopausal women with hormone receptor-positive early breast cancer. Anastrozole 130-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 179-195 24316735-3 2014 A sequence of molecular events leading to cellular demise is launched by a specific chemical compound, 1-(3,4,5-trihydroxyphenyl)nonan-1-one, newly acquired from screening a library of TR3-targeting compounds. 1-(3,4,5-trihydroxyphenyl)nonan-1-one 103-140 nuclear receptor subfamily 4 group A member 1 Homo sapiens 185-188 24463450-4 2014 We then applied information from this analysis to classify human breast tumors based on normal cell types into 4 major subtypes, HR0-HR3, which were differentiated by vitamin D, androgen, and estrogen hormone receptor (HR) expression. Vitamin D 167-176 nuclear receptor subfamily 4 group A member 1 Homo sapiens 129-131 24498071-4 2014 METHODS AND RESULTS: The Nur77 gene, a nuclear hormone receptor, was highly induced by treatment with Cytosporone B (Csn-B, specific Nur77 agonist), recombinant plasmid over-expressing Nur77 (pcDNA-Nur77), while inhibited by treatment with siRNAs against Nur77 (si-Nur77) in THP-1 macrophage-derived foam cells, HepG2 cells and Caco-2 cells, respectively. cytosporone B 102-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-30 24485460-4 2014 Integration of an endothelial genome-wide transcriptional profile with chromatin immunoprecipitation sequencing revealed that PR induces an NR4A1 (Nur77/TR3)-dependent transcriptional program that broadly regulates vascular permeability in response to progesterone. Progesterone 252-264 nuclear receptor subfamily 4 group A member 1 Homo sapiens 140-145 24498071-4 2014 METHODS AND RESULTS: The Nur77 gene, a nuclear hormone receptor, was highly induced by treatment with Cytosporone B (Csn-B, specific Nur77 agonist), recombinant plasmid over-expressing Nur77 (pcDNA-Nur77), while inhibited by treatment with siRNAs against Nur77 (si-Nur77) in THP-1 macrophage-derived foam cells, HepG2 cells and Caco-2 cells, respectively. cytosporone B 102-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-138 24498071-4 2014 METHODS AND RESULTS: The Nur77 gene, a nuclear hormone receptor, was highly induced by treatment with Cytosporone B (Csn-B, specific Nur77 agonist), recombinant plasmid over-expressing Nur77 (pcDNA-Nur77), while inhibited by treatment with siRNAs against Nur77 (si-Nur77) in THP-1 macrophage-derived foam cells, HepG2 cells and Caco-2 cells, respectively. cytosporone B 102-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-138 24498071-4 2014 METHODS AND RESULTS: The Nur77 gene, a nuclear hormone receptor, was highly induced by treatment with Cytosporone B (Csn-B, specific Nur77 agonist), recombinant plasmid over-expressing Nur77 (pcDNA-Nur77), while inhibited by treatment with siRNAs against Nur77 (si-Nur77) in THP-1 macrophage-derived foam cells, HepG2 cells and Caco-2 cells, respectively. cytosporone B 102-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-138 24498071-4 2014 METHODS AND RESULTS: The Nur77 gene, a nuclear hormone receptor, was highly induced by treatment with Cytosporone B (Csn-B, specific Nur77 agonist), recombinant plasmid over-expressing Nur77 (pcDNA-Nur77), while inhibited by treatment with siRNAs against Nur77 (si-Nur77) in THP-1 macrophage-derived foam cells, HepG2 cells and Caco-2 cells, respectively. cytosporone B 102-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 262-270 24485460-4 2014 Integration of an endothelial genome-wide transcriptional profile with chromatin immunoprecipitation sequencing revealed that PR induces an NR4A1 (Nur77/TR3)-dependent transcriptional program that broadly regulates vascular permeability in response to progesterone. Progesterone 252-264 nuclear receptor subfamily 4 group A member 1 Homo sapiens 147-152 24485460-4 2014 Integration of an endothelial genome-wide transcriptional profile with chromatin immunoprecipitation sequencing revealed that PR induces an NR4A1 (Nur77/TR3)-dependent transcriptional program that broadly regulates vascular permeability in response to progesterone. Progesterone 252-264 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-156 24272078-0 2014 Comparative efficacy of everolimus plus exemestane versus fulvestrant for hormone-receptor-positive advanced breast cancer following progression/recurrence after endocrine therapy: a network meta-analysis. Fulvestrant 58-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-90 24360559-4 2014 We define the unique molecular profile of a compound (SM145) that regulates hormone receptor protein levels through hsp90 inhibition without inducing the heat shock response. sm145 54-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-92 24857109-1 2014 Treatment with adjuvant endocrine therapy, including tamoxifen and the aromatase inhibitors, has resulted in notable improvements in disease-free and overall survival for patients with hormone receptor-positive breast cancer. Tamoxifen 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 185-201 24434530-1 2014 The selective estrogen receptor modulator, tamoxifen, is extensively used for the endocrine treatment of all stages of hormone receptor-positive breast cancer. Tamoxifen 43-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-135 24531914-7 2014 However, the levels of NGFIB expression were significantly higher in RSZ of IHA than in RSZ of adjacent adrenals of APA and the ZG of NA (P<0.05), which may partly account for the expression levels of 3beta-HSD among the three groups of adrenals. 3r0y 69-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-28 24531914-7 2014 However, the levels of NGFIB expression were significantly higher in RSZ of IHA than in RSZ of adjacent adrenals of APA and the ZG of NA (P<0.05), which may partly account for the expression levels of 3beta-HSD among the three groups of adrenals. 3r0y 88-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-28 24903080-0 2014 Validation and comparison of CS-IHC4 scores with a nomogram to predict recurrence in hormone receptor-positive breast cancers. Cesium 29-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 24531914-8 2014 These results may imply NGFIB plays important roles in the marked differences in steroidogenic functions in the two distinct types of RSZ of PA cases. 3r0y 134-137 nuclear receptor subfamily 4 group A member 1 Homo sapiens 24-29 24927845-3 2014 Genome-wide analysis of hormone receptor-related networks will provide new insights into the understanding of the molecular mechanism orchestrated by estrogen and androgen receptors, and will enable the development of new methods for the diagnosis and treatment of steroid hormone-related cancers. Steroids 265-280 nuclear receptor subfamily 4 group A member 1 Homo sapiens 24-40 24550751-0 2013 Cost-Effectiveness of Lapatinib plus Letrozole in Post-Menopausal Women with Hormone Receptor-and HER2-Positive Metastatic Breast Cancer. Lapatinib 22-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-93 24756805-3 2014 Everolimus has been approved by the FDA and the EMA for the treatment of advanced renal cell carcinoma (RCC), subependymal giant cell astrocytoma (SEGA) associated with tuberous sclerosis (TSC), pancreatic neuroendocrine tumors (PNET), in combination with exemestane in advanced hormone-receptor (HR)-positive, HER2-negative breast cancer. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 279-295 24756805-3 2014 Everolimus has been approved by the FDA and the EMA for the treatment of advanced renal cell carcinoma (RCC), subependymal giant cell astrocytoma (SEGA) associated with tuberous sclerosis (TSC), pancreatic neuroendocrine tumors (PNET), in combination with exemestane in advanced hormone-receptor (HR)-positive, HER2-negative breast cancer. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 297-299 24185007-7 2013 Expression of transcription factors activated downstream of MAP kinase and cAMP pathways also conferred resistance, including c-FOS, NR4A1, NR4A2 and MITF. Cyclic AMP 75-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-138 24550751-0 2013 Cost-Effectiveness of Lapatinib plus Letrozole in Post-Menopausal Women with Hormone Receptor-and HER2-Positive Metastatic Breast Cancer. Letrozole 37-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-93 24299210-5 2013 In our cell culture model, we also demonstrated that Nur77 competitively inhibits androgen-dependent transcription activity and more specifically, Nur77 competes with androgen receptor for binding to src-1, a well-known coactivator for steroids. Steroids 236-244 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-58 24299210-5 2013 In our cell culture model, we also demonstrated that Nur77 competitively inhibits androgen-dependent transcription activity and more specifically, Nur77 competes with androgen receptor for binding to src-1, a well-known coactivator for steroids. Steroids 236-244 nuclear receptor subfamily 4 group A member 1 Homo sapiens 147-152 24299210-6 2013 More importantly, we also showed that a small molecule agonist for Nur77, Cytosporone B, significantly inhibits androgen-dependent bladder cancer cell growth in two different cell lines. cytosporone B 74-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-72 24267730-1 2013 BACKGROUND: Postmenopausal women with hormone receptor-positive (HR(+)) breast cancer in whom disease progresses or there is recurrence while taking a nonsteroidal aromatase inhibitor (NSAI) are usually treated with exemestane (EXE), but no single standard of care exists in this setting. exemestane 216-226 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-54 23873636-9 2013 alpha,beta-methylene-ATP and beta,gamma-methylene-ATP applied for 30 min to 4 h increased the expression of NR4A1; NF449 blocked or attenuated this effect. alpha,beta-methyleneadenosine 5'-triphosphate 0-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-113 24335365-0 2013 [Assessment of the clinical efficacy and safety of fulvestrant in heavily pretreated patients with hormone-receptor positive metastatic breast cancer-a single-institution experience]. Fulvestrant 51-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-115 24335365-1 2013 Fulvestrant, a pure estrogen receptor antagonist with no known agonist effects, was approved in September 2011 for the treatment of hormone-receptor positive metastatic breast cancer(MBC)in postmenopausal women in Japan. Fulvestrant 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-148 23873636-9 2013 alpha,beta-methylene-ATP and beta,gamma-methylene-ATP applied for 30 min to 4 h increased the expression of NR4A1; NF449 blocked or attenuated this effect. 5'-adenylyl (beta,gamma-methylene)diphosphonate 29-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-113 23873636-10 2013 Small interfering RNA directed against NR4A1 diminished the antiproliferative effects of alpha,beta-methylene-ATP and beta,gamma-methylene-ATP. alpha,beta-methyleneadenosine 5'-triphosphate 89-113 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 23873636-10 2013 Small interfering RNA directed against NR4A1 diminished the antiproliferative effects of alpha,beta-methylene-ATP and beta,gamma-methylene-ATP. 5'-adenylyl (beta,gamma-methylene)diphosphonate 118-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 23873636-12 2013 In conclusion, our results demonstrate for the first time that adenine nucleotides acting at P2X1 receptors inhibit the proliferation of human coronary smooth muscle cells via the induction of the early gene NR4A1. Adenine Nucleotides 63-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 24371718-1 2013 Low-grade papillary serous ovarian carcinoma has unique epidemiologic and disease-specific characteristics Cyberknife radiotherapy is a unique treatment that may successfully be used to treat unresectable disease Anastrozole is an effective treatment for hormone receptor-positive low-grade papillary serous ovarian carcinoma. Anastrozole 213-224 nuclear receptor subfamily 4 group A member 1 Homo sapiens 255-271 24534345-5 2013 RESULTS: The 3-year recurrence free survival for HR+/HER2-, HER2+ and HR-/HER2- were 94.9%, 89.5% ane 92.3% respectively. camphene 98-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-51 24534345-5 2013 RESULTS: The 3-year recurrence free survival for HR+/HER2-, HER2+ and HR-/HER2- were 94.9%, 89.5% ane 92.3% respectively. camphene 98-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-72 24396871-0 2013 Palmitate increases Nur77 expression by modulating ZBP89 and Sp1 binding to the Nur77 proximal promoter in pancreatic beta-cells. Palmitates 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-25 24396871-0 2013 Palmitate increases Nur77 expression by modulating ZBP89 and Sp1 binding to the Nur77 proximal promoter in pancreatic beta-cells. Palmitates 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-85 24396871-1 2013 Nur77 is a stress sensor in pancreatic beta-cells, which negatively regulates glucose-stimulated insulin secretion. Glucose 78-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 24396871-2 2013 We recently showed that a lipotoxic shock caused by exposure of beta-cells to the saturated fatty acid palmitate strongly increases Nur77 expression. saturated fatty acid palmitate 82-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-137 24396871-4 2013 Chromatin immunoprecipitation, transient transfection and siRNA-mediated knockdown assays revealed that palmitate induced Nur77 promoter activation involves Sp1 recruitment and ZBP89 release from the gene promoter. Palmitates 104-113 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-127 24032657-1 2013 Amoitone B, a novel compound chemically synthesized as the analogue of cytosporone B, has been proved to own superior affinity with Nur77 than its parent compound and exhibit notable anticancer activity. n-amyl 2-(3,5-dihydroxy-2-(1-nonanoyl)phenyl)acetate 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-137 24032657-1 2013 Amoitone B, a novel compound chemically synthesized as the analogue of cytosporone B, has been proved to own superior affinity with Nur77 than its parent compound and exhibit notable anticancer activity. cytosporone B 71-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-137 24155635-0 2013 Cost-effectiveness of lapatinib plus letrozole in her2-positive, hormone receptor-positive metastatic breast cancer in Canada. Lapatinib 22-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 65-81 24155635-1 2013 BACKGROUND: The cost-effectiveness of first-line treatment with lapatinib plus letrozole for postmenopausal women with hormone receptor-positive (hr+), human epidermal growth factor receptor 2-positive (her2+) metastatic breast cancer (mbc) has not been assessed from the Canadian health care system and societal perspectives. Lapatinib 64-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-135 24155635-1 2013 BACKGROUND: The cost-effectiveness of first-line treatment with lapatinib plus letrozole for postmenopausal women with hormone receptor-positive (hr+), human epidermal growth factor receptor 2-positive (her2+) metastatic breast cancer (mbc) has not been assessed from the Canadian health care system and societal perspectives. Letrozole 79-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-135 24033101-3 2013 Several of the cardiac glycosides induced apoptosis in lung cancer cells, which was accompanied by induction of Nur77 protein expression. Glycosides 23-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-117 24033101-4 2013 Treatment of cancer cells with the cardiac glycosides resulted in translocation of the Nur77 protein from the nucleus to the cytoplasm and subsequent targeting to mitochondria. Glycosides 43-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-92 24033101-5 2013 The results show that the cardiac glycosides exert their apoptotic effect through the Nur77-dependent apoptotic pathway. Glycosides 34-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-91 24512852-0 2013 Palmitate increases Nur77 expression by modulating ZBP89 and Sp1 binding to the Nur77 proximal promoter in pancreatic beta-cells. Palmitates 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-25 24512852-0 2013 Palmitate increases Nur77 expression by modulating ZBP89 and Sp1 binding to the Nur77 proximal promoter in pancreatic beta-cells. Palmitates 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-85 24512852-1 2013 Nur77 is a stress sensor in pancreatic beta-cells, which negatively regulates glucose-stimulated insulin secretion. Glucose 78-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 24512852-2 2013 We recently showed that a lipotoxic shock caused by exposure of beta-cells to the saturated fatty acid palmitate strongly increases Nur77 expression. saturated fatty acid palmitate 82-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-137 24512852-4 2013 Chromatin immunoprecipitation, transient transfection and siRNA-mediated knockdown assays revealed that palmitate induced Nur77 promoter activation involves Sp1 recruitment and ZBP89 release from the gene promoter. Palmitates 104-113 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-127 23903894-7 2013 RESULTS: In peripheral blood mononuclear cells, Nur77 was significantly and consistently decreased 2 h after vorinostat administration on both days 1 and 9, median ratio of gene expression relative to baseline of 0.69 with interquartile range 0.49-1.04 (p < 0.001); 0.28 (0.15-0.7) (p < 0.001), respectively, with more pronounced decrease on day 9, when patients received both vorinostat and bortezomib. Vorinostat 109-119 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 23903894-7 2013 RESULTS: In peripheral blood mononuclear cells, Nur77 was significantly and consistently decreased 2 h after vorinostat administration on both days 1 and 9, median ratio of gene expression relative to baseline of 0.69 with interquartile range 0.49-1.04 (p < 0.001); 0.28 (0.15-0.7) (p < 0.001), respectively, with more pronounced decrease on day 9, when patients received both vorinostat and bortezomib. Vorinostat 383-393 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 23903894-7 2013 RESULTS: In peripheral blood mononuclear cells, Nur77 was significantly and consistently decreased 2 h after vorinostat administration on both days 1 and 9, median ratio of gene expression relative to baseline of 0.69 with interquartile range 0.49-1.04 (p < 0.001); 0.28 (0.15-0.7) (p < 0.001), respectively, with more pronounced decrease on day 9, when patients received both vorinostat and bortezomib. Bortezomib 398-408 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 23903894-8 2013 p21, a downstream target of Nur77, was significantly decreased on day 9, 2 and 6 h after administration of vorinostat and bortezomib, 0.67 (0.41-1.03) (p < 0.01); 0.44 (0.25-1.3) (p < 0.01), respectively. Vorinostat 107-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 23903894-8 2013 p21, a downstream target of Nur77, was significantly decreased on day 9, 2 and 6 h after administration of vorinostat and bortezomib, 0.67 (0.41-1.03) (p < 0.01); 0.44 (0.25-1.3) (p < 0.01), respectively. Bortezomib 122-132 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 23903894-9 2013 The ChIP assay demonstrated a protein-DNA interaction, in this case interaction of Nur77, HSP70 and p21 with acetylated histone H3, at baseline and at day 9 after treatment with vorinostat in tissue biopsies in most patients. Vorinostat 178-188 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-88 23903894-10 2013 CONCLUSION: Vorinostat inhibits Nur77 expression, which in turn may decrease p21 and AKT expression in PBMCs. Vorinostat 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-37 23831020-0 2013 Repression of NR4A1 by a chromatin modifier promotes docetaxel resistance in PC-3 human prostate cancer cells. Docetaxel 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-19 23836374-5 2013 In addition, chromatin immunoprecipitation-PCR, avidin-biotin-conjugated DNA precipitation, and luciferase reporter assays confirmed that NUR77 directly regulated the transcription of the inhibin-alpha gene through the specific NGFI-B response element located within its promoter. avidin-biotin 48-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 138-143 23982884-9 2013 The combination of letrozole and gonadotropin-releasing hormone analog is effective and safe in hormone-receptor positive, metastatic male breast cancer patients. Letrozole 19-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-112 23860520-11 2013 CONCLUSION: The data from the current study demonstrated that the addition of goserelin to TAM results in downregulation of estradiol level, followed by significant reduction in BD and ET in premenopausal and perimenopausal women with hormone receptor-positive breast cancer, which may eventually lead to better outcome in these patients. tam 91-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 235-251 23720056-0 2013 TR3 modulates platinum resistance in ovarian cancer. Platinum 14-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-3 23720056-4 2013 Moreover, TR3 expression was significantly lower in platinum-resistant tumors in patients with metastatic disease, and low TR3 staining was associated with poorer overall and progression-free survival. Platinum 52-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-13 23720056-5 2013 We have identified a direct role for TR3 in cisplatin-induced apoptosis in ovarian cancer cells. Cisplatin 44-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-40 23720056-6 2013 Nucleus-to-cytoplasm translocation of TR3 was observed in cisplatin-sensitive (OVCAR8, OVCAR3, and A2780PAR) but not cisplatin-resistant (NCI/ADR-RES and A2780CP20) ovarian cancer cells. Cisplatin 58-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-41 23720056-6 2013 Nucleus-to-cytoplasm translocation of TR3 was observed in cisplatin-sensitive (OVCAR8, OVCAR3, and A2780PAR) but not cisplatin-resistant (NCI/ADR-RES and A2780CP20) ovarian cancer cells. Cisplatin 117-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-41 23720056-7 2013 Immunofluorescent analyses showed clear overlap between TR3 and mitochondrial Hsp60 in cisplatin-treated cells, which was associated with cytochrome c release. Cisplatin 87-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 56-59 23720056-8 2013 Ovarian cancer cells with stable shRNA- or transient siRNA-mediated TR3 downregulation displayed substantial reduction in cisplatin effects on apoptotic markers and cell growth in vitro and in vivo. Cisplatin 122-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-71 23720056-9 2013 Mechanistic studies showed that the cisplatin-induced cytoplasmic TR3 translocation required for apoptosis induction was regulated by JNK activation and inhibition of Akt. Cisplatin 36-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-69 23720056-10 2013 Finally, cisplatin resistance was partially overcome by ectopic TR3 overexpression and by treatment with the JNK activator anisomycin and Akt pathway inhibitor, wortmannin. Cisplatin 9-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-67 24074783-6 2013 Recent data demonstrating that 10 years of tamoxifen improves outcomes compared to 5 may be particularly beneficial for young women with hormone receptor-positive tumors given the risk benefit profile. Tamoxifen 43-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-153 24415983-0 2013 Everolimus in postmenopausal, hormone receptor-positive advanced breast cancer: summary and results of an austrian expert panel discussion. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-46 23720056-11 2013 Our results suggest that disruption of TR3 activity, via downregulation or nuclear sequestration, likely contributes to platinum resistance in ovarian cancer. Platinum 120-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-42 23720056-12 2013 Moreover, we have described a treatment strategy aimed at overcoming platinum resistance by targeting TR3. Platinum 69-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-105 23997526-2 2013 METHODS: Consecutive 160 postmenopausal women with T1-3N0-1M0 hormone receptor (HR)-positive invasive breast cancer were treated with anastrozole for 16 weeks before surgery. Anastrozole 134-145 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-78 23997526-2 2013 METHODS: Consecutive 160 postmenopausal women with T1-3N0-1M0 hormone receptor (HR)-positive invasive breast cancer were treated with anastrozole for 16 weeks before surgery. Anastrozole 134-145 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-82 23663895-0 2013 NR4A1 enhances neural survival following oxygen and glucose deprivation: an in vitro study. Oxygen 41-47 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 23829891-8 2013 In the multivariate analysis, patients with long-term clinical benefit had a higher likelihood of having hormone receptor-positive tumors (odds ratio [OR]positive vs. negative = 2.39 [95% confidence interval (CI), 1.08-5.31]; P = .032); and a lower likelihood of having received adjuvant trastuzumab (ORadjuvant trastuzumab vs. no adjuvant trastuzumab = 0.30 [95% CI, 0.10-0.96]; P = .043]. oradjuvant 301-311 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-121 23660295-6 2013 When stimulated with 12-O-tetradecanoylphorbol 13-acetate (TPA) or CD437, this TR3-TRAPgamma interaction not only induced Ca(2+) depletion in the endoplasmic reticulum (ER) but also promoted the expression of the proapoptotic transcriptional regulator CHOP. Tetradecanoylphorbol Acetate 21-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-82 23660295-6 2013 When stimulated with 12-O-tetradecanoylphorbol 13-acetate (TPA) or CD437, this TR3-TRAPgamma interaction not only induced Ca(2+) depletion in the endoplasmic reticulum (ER) but also promoted the expression of the proapoptotic transcriptional regulator CHOP. Tetradecanoylphorbol Acetate 59-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-82 23660295-6 2013 When stimulated with 12-O-tetradecanoylphorbol 13-acetate (TPA) or CD437, this TR3-TRAPgamma interaction not only induced Ca(2+) depletion in the endoplasmic reticulum (ER) but also promoted the expression of the proapoptotic transcriptional regulator CHOP. CD 437 67-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-82 23686401-2 2013 Results from the phase III BOLERO-2 trial demonstrated that everolimus in combination with exemestane provided significant clinical benefit to patients with advanced hormone receptor-positive breast cancer. Everolimus 60-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-182 23686401-2 2013 Results from the phase III BOLERO-2 trial demonstrated that everolimus in combination with exemestane provided significant clinical benefit to patients with advanced hormone receptor-positive breast cancer. exemestane 91-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-182 23904760-2 2013 The present retrospective study compared the efficacy and safety of toremifene and tamoxifen in the treatment of operable hormone receptor-positive breast cancer in premenopausal women. Toremifene 68-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-138 23904760-2 2013 The present retrospective study compared the efficacy and safety of toremifene and tamoxifen in the treatment of operable hormone receptor-positive breast cancer in premenopausal women. Tamoxifen 83-92 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-138 23904760-13 2013 CONCLUSIONS: In this retrospective study, the efficacy and safety profiles of toremifene and tamoxifen for the treatment of operable hormone receptor-positive breast cancer in premenopausal women were similar. Toremifene 78-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-149 23904760-13 2013 CONCLUSIONS: In this retrospective study, the efficacy and safety profiles of toremifene and tamoxifen for the treatment of operable hormone receptor-positive breast cancer in premenopausal women were similar. Tamoxifen 93-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-149 23686401-0 2013 Management of adverse events in patients with hormone receptor-positive breast cancer treated with everolimus: observations from a phase III clinical trial. Everolimus 99-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-62 23686401-1 2013 Everolimus is a mammalian target of rapamycin (mTOR) inhibitor approved for the treatment of advanced renal cell carcinoma, pancreatic neuroendocrine tumors, subependymal giant cell astrocytoma associated with tuberous sclerosis complex, renal angiomyolipoma and tuberous sclerosis complex, and, in combination with exemestane, for hormone receptor-positive HER2-negative advanced breast cancer after failure of treatment with letrozole or anastrozole. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 332-348 23663895-4 2013 Our results showed that oxygen and glucose deprivation (OGD) dramatically induced primary culture neural cell apoptosis and NR4A1 expression at both protein and mRNA level. Oxygen 24-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 124-129 23551242-10 2013 Interestingly, within the haloperidol-treated group, TD-free animals showed higher Nur77 expression in putamen subterritories compared with dyskinetic animals. Haloperidol 26-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-88 23874725-4 2013 Our studies confirm that the HSD3B2 promoter is regulated by transcription factors GATA, Nur77 and SF1/LRH1 in concert and that the NBRE/Nur77 site is crucial for hormonal stimulation with cAMP. Cyclic AMP 189-193 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-142 23715630-0 2013 A randomized, double-blind, controlled study of exemestane versus anastrozole for the first-line treatment of postmenopausal Japanese women with hormone-receptor-positive advanced breast cancer. exemestane 48-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-161 23755153-6 2014 Tamoxifen treatment significantly altered the hormone receptor expression levels of the tumor, while additionally upregulating Bcl-2 and Cyclin D1. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-62 23551242-0 2013 Haloperidol-induced striatal Nur77 expression in a non-human primate model of tardive dyskinesia. Haloperidol 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-34 23551242-9 2013 Postmortem analysis of Nur77 expression measured by in situ hybridization revealed a stark contrast between the two drugs, as Nur77 mRNA levels in the caudate-putamen were strongly upregulated in animals exposed to haloperidol but were spared following clozapine treatment. Haloperidol 215-226 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-28 23551242-9 2013 Postmortem analysis of Nur77 expression measured by in situ hybridization revealed a stark contrast between the two drugs, as Nur77 mRNA levels in the caudate-putamen were strongly upregulated in animals exposed to haloperidol but were spared following clozapine treatment. Haloperidol 215-226 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-131 23551242-9 2013 Postmortem analysis of Nur77 expression measured by in situ hybridization revealed a stark contrast between the two drugs, as Nur77 mRNA levels in the caudate-putamen were strongly upregulated in animals exposed to haloperidol but were spared following clozapine treatment. Clozapine 253-262 nuclear receptor subfamily 4 group A member 1 Homo sapiens 23-28 23715630-1 2013 The aromatase inhibitors exemestane and anastrozole are approved in Japan for first-line treatment of postmenopausal patients with advanced, hormone-receptor-positive breast cancer. exemestane 25-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 141-157 23715630-1 2013 The aromatase inhibitors exemestane and anastrozole are approved in Japan for first-line treatment of postmenopausal patients with advanced, hormone-receptor-positive breast cancer. Anastrozole 40-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 141-157 23819026-2 2013 In young women with hormone-receptor positive disease, 5 years of adjuvant tamoxifen, with or without ovarian suppression/ablation, is considered the standard endocrine therapy. Tamoxifen 75-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-36 23187735-4 2013 Importantly we identify a molecular mechanism involving sitagliptin-mediated attenuation of TNFalpha-mediated induction of NFkappaB and orphan nuclear receptor NUR77 mRNA expression, also able to be reproduced, in part, independent of GLP-1. Sitagliptin Phosphate 56-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-165 23247046-0 2013 HDAC inhibition by SNDX-275 (Entinostat) restores expression of silenced leukemia-associated transcription factors Nur77 and Nor1 and of key pro-apoptotic proteins in AML. entinostat 19-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-120 23247046-5 2013 We here report that inhibition of histone deacetylase (HDAC) using the specific class I HDAC inhibitor SNDX-275 restored the expression of Nur77/Nor1 and induced expression of activator protein 1 transcription factors c-Jun and JunB, and of death receptor TRAIL, in AML cells and in CD34(+)/38(-) AML LSCs. entinostat 103-111 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 23247046-6 2013 Importantly, SNDX-275 induced extensive apoptosis in AML cells, which could be suppressed by silencing nur77 and nor1. entinostat 13-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-108 23580071-1 2013 Tamoxifen is a widely utilized adjuvant anti-estrogen agent for hormone receptor-positive breast cancer, known to undergo CYP2D6-mediated bioactivation to endoxifen. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-80 23580071-1 2013 Tamoxifen is a widely utilized adjuvant anti-estrogen agent for hormone receptor-positive breast cancer, known to undergo CYP2D6-mediated bioactivation to endoxifen. 4-hydroxy-N-desmethyltamoxifen 155-164 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-80 23425564-11 2013 CONCLUSION: These exploratory analyses suggest that everolimus has beneficial effects on bone turnover and progressive disease in bone in patients receiving exemestane for hormone receptor-positive breast cancer progressing during/after nonsteroidal aromatase inhibitor therapy. Everolimus 52-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 172-188 23425564-11 2013 CONCLUSION: These exploratory analyses suggest that everolimus has beneficial effects on bone turnover and progressive disease in bone in patients receiving exemestane for hormone receptor-positive breast cancer progressing during/after nonsteroidal aromatase inhibitor therapy. exemestane 157-167 nuclear receptor subfamily 4 group A member 1 Homo sapiens 172-188 23391443-3 2013 Both salmon calcitonin (sCT) and hyaluronic acid (HA) attenuated activated mRNA expression of NR4A1, NR4A2, NR4A3, and matrix metalloproteinases (MMPs) 1, 3 and 13 in three human cell lines: SW1353 chondrocytes, U937 and THP-1 monocytes. Hyaluronic Acid 33-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 23391443-3 2013 Both salmon calcitonin (sCT) and hyaluronic acid (HA) attenuated activated mRNA expression of NR4A1, NR4A2, NR4A3, and matrix metalloproteinases (MMPs) 1, 3 and 13 in three human cell lines: SW1353 chondrocytes, U937 and THP-1 monocytes. Hyaluronic Acid 50-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 23315169-0 2013 The vascular permeabilizing factors histamine and serotonin induce angiogenesis through TR3/Nur77 and subsequently truncate it through thrombospondin-1. Histamine 36-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-91 23315169-0 2013 The vascular permeabilizing factors histamine and serotonin induce angiogenesis through TR3/Nur77 and subsequently truncate it through thrombospondin-1. Histamine 36-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-97 23315169-0 2013 The vascular permeabilizing factors histamine and serotonin induce angiogenesis through TR3/Nur77 and subsequently truncate it through thrombospondin-1. Serotonin 50-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-91 23315169-0 2013 The vascular permeabilizing factors histamine and serotonin induce angiogenesis through TR3/Nur77 and subsequently truncate it through thrombospondin-1. Serotonin 50-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-97 23358971-13 2013 Exemestane should be considered another option as up-front adjuvant therapy for postmenopausal hormone receptor-positive breast cancer. exemestane 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 95-111 23359049-8 2013 The DSS benefit with BCT compared with mastectomy was greater among women age >= 50 with HR-positive disease (hazard ratio = 0.86, 95% CI = 0.82-0.91) than among women age < 50 with HR-negative disease (hazard ratio = 0.88, 95% CI = 0.79-0.98); however, this trend was seen among all subgroups analyzed. dss 4-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-94 23359049-8 2013 The DSS benefit with BCT compared with mastectomy was greater among women age >= 50 with HR-positive disease (hazard ratio = 0.86, 95% CI = 0.82-0.91) than among women age < 50 with HR-negative disease (hazard ratio = 0.88, 95% CI = 0.79-0.98); however, this trend was seen among all subgroups analyzed. Bicarbonates 21-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-94 23538253-2 2013 Evolving understanding of the metabolism and pharmacogenomics of tamoxifen, an early example of targeted therapy for women with hormone receptor-positive breast cancer, has created decision-making challenges for healthcare providers and their patients. Tamoxifen 65-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 128-144 23450278-0 2013 Epirubicin and docetaxel as neoadjuvant treatment of hormone receptor positive, HER-2 negative breast cancer: findings from two successive phase II studies. Epirubicin 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-69 23450278-1 2013 BACKGROUND: We report on the activity of the combination of epirubicin and docetaxel given in neoadjuvant setting for 4 and 8 cycles respectively in 2 successive series of patients with large operable or locally advanced, hormone receptor positive, HER-2 negative breast cancer. Epirubicin 60-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 222-238 23450278-1 2013 BACKGROUND: We report on the activity of the combination of epirubicin and docetaxel given in neoadjuvant setting for 4 and 8 cycles respectively in 2 successive series of patients with large operable or locally advanced, hormone receptor positive, HER-2 negative breast cancer. Docetaxel 75-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 222-238 23053261-0 2013 Phase I trial of exemestane in combination with metformin and rosiglitazone in nondiabetic obese postmenopausal women with hormone receptor-positive metastatic breast cancer. exemestane 17-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-139 23184079-9 2013 Our study supported that hormonal therapy, whether in the form of an aromatase inhibitor or tamoxifen, confers a survival benefit when added to chemotherapy and trastuzumab in patients with HR-positive/HER2-positive primary breast cancer. Tamoxifen 92-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 190-192 23224235-8 2013 Tamoxifen should be considered as the treatment of choice for hormone-receptor-positive male breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-78 26909267-11 2013 This large, retrospective study demonstrates a significant survival benefit with adjuvant bisphosphonates in patients with early breast cancer, particularly in patients with node-positive and hormone receptor-positive disease. Diphosphonates 90-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 192-208 23053261-0 2013 Phase I trial of exemestane in combination with metformin and rosiglitazone in nondiabetic obese postmenopausal women with hormone receptor-positive metastatic breast cancer. Rosiglitazone 62-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-139 23053261-3 2013 We investigated the tolerability and pharmacokinetics of exemestane in combination with metformin and rosiglitazone in nondiabetic overweight and obese postmenopausal women with hormone receptor-positive metastatic breast cancer. exemestane 57-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 178-194 23012478-4 2012 The overall N10 structures are similar to each other and to other known influenza NA structures, with a single highly conserved calcium binding site in each monomer. Calcium 128-135 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-15 22994502-0 2012 Everolimus in the treatment of hormone receptor-positive breast cancer. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-48 22674155-9 2012 Histamine modulated the expression of NR4A1-3 orphan receptors in primary and immortalized human chondrocyte cells in a time- and concentration-dependent manner. Histamine 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 22553196-7 2012 CONCLUSIONS: The addition of everolimus to exemestane for women with HR-positive metastatic BC is now considered a new therapeutic strategy. Everolimus 29-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-71 22553196-7 2012 CONCLUSIONS: The addition of everolimus to exemestane for women with HR-positive metastatic BC is now considered a new therapeutic strategy. exemestane 43-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-71 23058912-3 2012 cAMP/dexamethasone (Dex) significantly increased BTG2 and other gluconeogenic genes such as Nur77, phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6-phosphatase (G6Pase) in hepatocytes. Cyclic AMP 0-4 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-97 23058912-3 2012 cAMP/dexamethasone (Dex) significantly increased BTG2 and other gluconeogenic genes such as Nur77, phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6-phosphatase (G6Pase) in hepatocytes. Dexamethasone 5-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-97 23058912-3 2012 cAMP/dexamethasone (Dex) significantly increased BTG2 and other gluconeogenic genes such as Nur77, phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6-phosphatase (G6Pase) in hepatocytes. dex 20-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-97 22622474-3 2012 We reported that high PCNA(+) TAM counts were associated with hormone receptor (HR)-negative, high-grade tumors and early recurrence. Tamoxifen 30-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-78 22622474-3 2012 We reported that high PCNA(+) TAM counts were associated with hormone receptor (HR)-negative, high-grade tumors and early recurrence. Tamoxifen 30-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-82 22674155-13 2012 Stable knockdown of NR4A1-3 expression resulted in reduced endogenous OPG levels and the loss of histamine-dependent regulation of RANKL expression. Histamine 97-106 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-25 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Serine 41-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Serine 41-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Serine 252-255 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Proline 261-264 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Proline 261-264 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Proline 261-264 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Proline 261-264 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Serine 41-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Serine 41-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Threonine 45-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Threonine 45-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Threonine 45-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Threonine 45-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Proline 49-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Proline 49-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Proline 49-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Proline 49-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Serine 252-255 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Serine 252-255 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 22789442-7 2012 A systematic mutation analysis of all 17 Ser/Thr-Pro-motifs in Nur77 revealed that Pin1 enhances protein stability of Nur77 in an isomerase-dependent manner by acting on phosphorylated Nur77 involving protein kinase CK2-mediated phosphorylation of the Ser(152)-Pro(153) motif in Nur77. Serine 252-255 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 23997516-16 2012 The standard treatment for all HR positive patients was administration of tamoxifen. Tamoxifen 74-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-33 22803611-2 2012 In this paper, we have employed time-resolved resonance Raman (TR3) spectroscopy to understand solvent-induced subtle structural changes in the lowest excited triplet state of thioxanthone. thioxanthone 176-188 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-66 22912978-0 2012 Developing in vitro reporter gene assays to assess the hormone receptor activities of chemicals frequently detected in drinking water. Drinking Water 119-133 nuclear receptor subfamily 4 group A member 1 Homo sapiens 55-71 22270929-11 2012 The improvement in DFS with docetaxel-containing regimens was observed across all subgroups (age, under or over 50; number of involved nodes; hormone receptor or HER2 status (including triple negative status), or administration schedule (sequential or concomitant). Docetaxel 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 142-158 22579996-1 2012 Amoitone B, as a new derivative of cytosporone B, has been proved to be a natural agonist for Nur77. n-amyl 2-(3,5-dihydroxy-2-(1-nonanoyl)phenyl)acetate 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 22579996-1 2012 Amoitone B, as a new derivative of cytosporone B, has been proved to be a natural agonist for Nur77. cytosporone B 35-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 22002310-3 2012 There are at least three phospho-Ser-Pro motifs on TR3 that bind to Pin1. Serine 33-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-54 22081070-6 2012 1,1-Bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) is a recently discovered inhibitor of TR3, which mimics the effects of siTR3. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 0-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-102 22081070-6 2012 1,1-Bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) is a recently discovered inhibitor of TR3, which mimics the effects of siTR3. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 48-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-102 22988612-1 2012 Four different textile preparation effluents were simulated to examine the applicability of the hydrogen peroxide/ultraviolet-C (H2O2/UV-C) advanced oxidation process for the treatment of real textile preparation (desizing, scouring and bleaching) wastewater bearing the non-ionic surfactant nonyl phenol decaethoxylate (NP-10). Hydrogen Peroxide 96-113 nuclear receptor subfamily 4 group A member 1 Homo sapiens 321-326 22988612-2 2012 In the absence of any textile preparation chemical, NP-10 degradation was complete in 15 min (rate coefficient: 0.22 min(-1)) accompanied by 78% chemical oxygen demand (COD) (rate coefficient: 0.026 min(-1)) and 57% total organic carbon (TOC) (rate coefficient: 0.014 min(-1)) removals achieved after 60 min photochemical treatment. Oxygen 154-160 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-57 22988612-2 2012 In the absence of any textile preparation chemical, NP-10 degradation was complete in 15 min (rate coefficient: 0.22 min(-1)) accompanied by 78% chemical oxygen demand (COD) (rate coefficient: 0.026 min(-1)) and 57% total organic carbon (TOC) (rate coefficient: 0.014 min(-1)) removals achieved after 60 min photochemical treatment. Carbon 230-236 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-57 22988612-4 2012 The organic, phosphonate-based sequestering agents competed with NP-10 for UV-C light absorption and HO* radicals. Organophosphonates 13-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 65-70 22988612-8 2012 For this textile preparation effluent, NP-10 degradation was complete after 50 min (rate coefficient: 0.061 min(-1)) exposure to H2O2/UV-C treatment. Hydrogen Peroxide 129-133 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 21945605-7 2012 In both cases the hormone receptor recruits an ATP-dependent chromatin remodeler, whose binding to chromatin is stabilized by distinct histone modifications. Adenosine Triphosphate 47-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-34 22002310-3 2012 There are at least three phospho-Ser-Pro motifs on TR3 that bind to Pin1. Proline 37-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-54 22425607-10 2012 The meta-analysis demonstrated that DD therapy can improve DFS (3356 patients; HR=0.83; 95% CI 0.73-0.95; p=0.005), independent of hormone receptor expression status. dd 36-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 131-147 21986938-8 2012 DLC-induced Nur77 protein was mainly found in the cytoplasm, and inhibition of Nur77 nuclear export by the CRM1-dependent nuclear export inhibitor leptomycin B or Jun N-terminal kinase inhibitor prevented the effect of DLC on inducing beta-catenin degradation. leptomycin B 147-159 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-17 22688624-1 2012 Tamoxifen is a mainstay in the treatment of hormone-receptor sensitive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-60 22470048-0 2012 The orphan nuclear receptor Nur77 regulates hepatic cholesterol metabolism through the suppression of LDLR and HMGCR expression. Cholesterol 52-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 22470048-3 2012 In order to investigate whether Nur77 is capable of regulating cholesterol metabolism in HepG2 cells and to demonstrate the underlying mechanism, the downregulation and upregulation of Nur77 expression in HepG2 cells was achieved by the transfection of siRNA specific to Nur77 and the transfection of the recombinant plasmid, pcDNA3.1-Nur77, respectively. Cholesterol 63-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-37 22470048-7 2012 As for the hepatic cholesterol metabolism genes, low-density lipoprotein receptor (LDLR) and HMGCoA reductase (HMGCR) levels increased following the downregulation of Nur77 expression and decreased following the upregulation of Nur77 expression. Cholesterol 19-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 167-172 22470048-9 2012 According to these findings, we conclude that Nur77 is capable of reducing hepatic cholesterol based on lipid overloading, and that this may be due to the decrease in LDLR and HMGCR levels. Cholesterol 83-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-51 21986938-8 2012 DLC-induced Nur77 protein was mainly found in the cytoplasm, and inhibition of Nur77 nuclear export by the CRM1-dependent nuclear export inhibitor leptomycin B or Jun N-terminal kinase inhibitor prevented the effect of DLC on inducing beta-catenin degradation. leptomycin B 147-159 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-84 29702826-2 2012 For treatment of postmenopausal, hormone receptor positive early stage breast cancer, tamoxifen or aromatase inhibitors such as anastrozole are prescribed either as first-line therapy or sequentially. Tamoxifen 86-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-49 22370313-3 2012 METHODS: We developed a Markov state transition model to simulate clinical practice and outcomes in a hypothetical cohort of women age 60 years with HR-positive EBC starting a 5-year course of AI therapy after primary surgery for breast cancer. NSC638702 161-164 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-151 29702826-2 2012 For treatment of postmenopausal, hormone receptor positive early stage breast cancer, tamoxifen or aromatase inhibitors such as anastrozole are prescribed either as first-line therapy or sequentially. Anastrozole 128-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-49 22306153-8 2012 CONCLUSIONS: We provide novel evidence demonstrating that the anti-inflammatory effects of minocycline in human monocytes include, in addition to decreased NF-kappaB activation, abrogation of the LPS-stimulated LOX-1, LITAF, Nur77 pathways, p38 MAPK inhibition and PI3K/Akt activation. Minocycline 91-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 225-230 22236200-4 2012 Approximately, 90% of patients received adjuvant chemotherapy and hormonal therapy with tamoxifen for hormone-receptor (HR)-positive breast cancer. Tamoxifen 88-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-118 22306153-6 2012 Minocycline inhibited LPS-induced activation of the lectin-like oxidized low density lipoprotein receptor-1 (LOX-1), NF-kappaB, LPS-induced TNF-alpha factor (LITAF) and the Nur77 nuclear receptor. Minocycline 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 173-178 25436706-1 2012 UNLABELLED: Abstract Background: Thyroid-stimulating hormone receptor (TSHR) is one of the members of glycoprotein hormone receptor family; activation of TSHR by thyroid-stimulating hormone (TSH) regulates thyroid function, proliferation, and differentiation. Thyrotropin 162-189 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-69 25436706-1 2012 UNLABELLED: Abstract Background: Thyroid-stimulating hormone receptor (TSHR) is one of the members of glycoprotein hormone receptor family; activation of TSHR by thyroid-stimulating hormone (TSH) regulates thyroid function, proliferation, and differentiation. Thyrotropin 71-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-69 22664513-4 2012 From these blocks hormone receptor expression was assessed by immunohistochemistry using the technique of streptoavidin-biotin-immunoperoxidase and anti-ER and anti-PR primary antibodies. Biotin 120-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-34 22306153-0 2012 Minocycline ameliorates LPS-induced inflammation in human monocytes by novel mechanisms including LOX-1, Nur77 and LITAF inhibition. Minocycline 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-110 22236200-4 2012 Approximately, 90% of patients received adjuvant chemotherapy and hormonal therapy with tamoxifen for hormone-receptor (HR)-positive breast cancer. Tamoxifen 88-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-122 21862331-6 2012 The eLEcTRA trial showed that the combination of letrozole and trastuzumab is a safe and effective treatment option for patients with HER2 positive and HR positive MBC. Letrozole 49-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 152-154 21761396-8 2012 CONCLUSIONS: BRCA1-associated, HRec-negative metastatic breast cancer patients were less sensitive to taxane chemotherapy than sporadic HRec-negative patients. taxane 102-108 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-35 21761396-9 2012 HRec-positive BRCA1- and BRCA2-associated patients had a sensitivity to taxane chemotherapy similar to that of sporadic patients. taxane 72-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-4 20809206-0 2012 Expression of Nur77 induced by an n-butylidenephthalide derivative promotes apoptosis and inhibits cell growth in oral squamous cell carcinoma. butylidenephthalide 34-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-19 22172646-3 2012 METHODS: The IDEAL trial is a prospective, open-label phase-III trial comparing 2.5 with 5 years of extended adjuvant letrozole (LET) in hormone receptor positive (HR+) postmenopausal early breast-cancer patients after 5 years of adjuvant endocrine therapy (ET). Letrozole 118-127 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-153 22531359-1 2012 Tamoxifen is an effective antiestrogen used in the treatment of hormone receptor-positive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-80 22610153-4 2012 Radiotherapy was mandatory after conservative surgery and tamoxifen was given for 5 years to hormone receptor (HR)-positive patients. Tamoxifen 58-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-109 22610153-4 2012 Radiotherapy was mandatory after conservative surgery and tamoxifen was given for 5 years to hormone receptor (HR)-positive patients. Tamoxifen 58-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-113 22396769-9 2012 Meanwhile, the subgroup analysis revealed that capecitabine improved the DFS in triple negative (HR = 0.71, 95% CI: 0.53-0.96, P = 0.028), hormone receptor negative (HR = 0.73, CI: 0.56-0.94, P = 0.017) and HER2 negative (HR = 0.81, CI: 0.67-0.98, P = 0.034) patients. Capecitabine 47-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-155 24367183-0 2011 Clinical utility of the combination of lapatinib and letrozole in the management of hormone receptor-positive and HER2-positive advanced breast cancer. Lapatinib 39-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-100 22077320-5 2011 NR4A1 and NR4A3 expression was also induced by Cu ions released into the medium. Copper 47-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 22068628-1 2011 Third-generation aromatase inhibitors (AIs) have proven to be superior to tamoxifen in terms of time to disease progression in patients with hormone receptor (HR) positive (HR+) status and, nowadays, are used in the adjuvant and neoadjuvant settings, and first-line therapy for advanced breast cancer. Tamoxifen 74-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 141-157 22068628-12 2011 In fact, the coadministration of both agents seems to increase the efficacy of letrozole in newly-diagnosed HR+ patients. Letrozole 79-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-110 22068628-13 2011 Once resistance to sequential trastuzumab and AI as monotherapy has been found, trastuzumab and letrozole combined in HR+ and HER2+ patients with advanced breast cancer can overcome resistance to both drugs administered as single agents, according to recently reported results. Letrozole 96-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-120 21936511-1 2011 Using the minima hopping global geometry optimization method on density functional potential energy surface, we have studied the structural and electronic properties of magnesium clusters for a size range of Mg(N) where N = 10-56. Magnesium 169-178 nuclear receptor subfamily 4 group A member 1 Homo sapiens 220-226 21903773-0 2011 A phase 2 trial of dasatinib in patients with advanced HER2-positive and/or hormone receptor-positive breast cancer. Dasatinib 19-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-92 21903773-2 2011 A phase 2 trial of dasatinib, a potent oral tyrosine kinase inhibitor of SFKs, was carried out in patients with human epidermal growth factor receptor 2-positive (HER2+) and/or hormone receptor-positive (HR+) advanced breast cancer. Dasatinib 19-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 177-193 24367183-0 2011 Clinical utility of the combination of lapatinib and letrozole in the management of hormone receptor-positive and HER2-positive advanced breast cancer. Letrozole 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-100 21907028-4 2011 The nitrate system featured a limit of detection of 0.04 mg N L(-1), 0.4%RSD (1 mg N L(-1) as nitrate, n=10), a coefficient of determination (R(2)) of 0.9995 over the calibration range 0.0-2.0 mg N L(-1), and a data acquisition time of 1.5s per spectrum. Nitrates 4-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-107 21907028-5 2011 The total nitrogen system featured a limit of detection of 0.05 mg N L(-1), 1%RSD (1 mg N L(-1) as ammonium chloride, n=10), a coefficient of determination of 0.9989 over the calibration range 0.0-2.0 mg N L(-1), and a throughput of 5 sample h(-1) measured in triplicate. Nitrogen 10-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-122 21945431-2 2011 We found that the cytosolic levels of NGFI-B and RXRalpha were increased in cultures of cerebellar granule neurons 2h after treatment with glutamate (excitatory neurotransmitter in the brain, involved in stroke). Deuterium 115-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-44 21945431-2 2011 We found that the cytosolic levels of NGFI-B and RXRalpha were increased in cultures of cerebellar granule neurons 2h after treatment with glutamate (excitatory neurotransmitter in the brain, involved in stroke). Glutamic Acid 139-148 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-44 21945431-0 2011 Delayed translocation of NGFI-B/RXR in glutamate stimulated neurons allows late protection by 9-cis retinoic acid. Glutamic Acid 39-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-31 21945431-6 2011 The RXR ligand 9-cis retinoic acid was used to arrest NGFI-B and RXR in the nucleus. Alitretinoin 15-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-60 21945431-0 2011 Delayed translocation of NGFI-B/RXR in glutamate stimulated neurons allows late protection by 9-cis retinoic acid. Alitretinoin 94-113 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-31 21945431-7 2011 Addition of 9-cis retinoic acid 1h after treatment with glutamate reduced the cytosolic translocation of NGFI-B and RXRalpha, the cytosolic translocation of NGFI-Bgfp observed in live neurons, as well as the neuronal death. 9-cis retinoic acid 1h 12-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-111 21945431-7 2011 Addition of 9-cis retinoic acid 1h after treatment with glutamate reduced the cytosolic translocation of NGFI-B and RXRalpha, the cytosolic translocation of NGFI-Bgfp observed in live neurons, as well as the neuronal death. Glutamic Acid 56-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-111 21813404-0 2011 Postmenopausal serum sex steroids and risk of hormone receptor-positive and -negative breast cancer: a nested case-control study. Steroids 25-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-62 21813404-2 2011 While evidence toward the existence of distinct subtypes of breast cancer accumulates, few studies have investigated the associations of sex steroid hormone levels with risk of hormone receptor [estrogen receptor (ER) and/or progesterone receptor (PR)] defined breast cancer. Steroids 141-156 nuclear receptor subfamily 4 group A member 1 Homo sapiens 177-193 21170551-2 2011 METHODS: Patients received exemestane or tamoxifen as adjuvant therapy for hormone receptor-positive breast cancer. exemestane 27-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 21228009-8 2011 Knockdown of Nur77 rescued hydrogen peroxide-induced cardiomyocyte apoptosis. Hydrogen Peroxide 27-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 21665134-12 2011 CONCLUSION: Bevacizumab combined with either anastrozole or fulvestrant was feasible and active in the first-line treatment of patients who have hormone receptor-positive metastatic breast cancer. Fulvestrant 60-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-161 21802721-1 2011 BACKGROUND: As trials of 5 years of tamoxifen in early breast cancer mature, the relevance of hormone receptor measurements (and other patient characteristics) to long-term outcome can be assessed increasingly reliably. Tamoxifen 36-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-110 20842526-5 2011 The presence of intratumoral promacs was significantly correlated with high grade, hormone receptor negative tumors, and a basal-like subtype. promacs 29-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-99 21681327-2 2011 Herein, we report the first study for developing mesoporous silica functionalized with phosphonate (NP10) as a sorbent for U(VI) sorption from aqueous solution. Silicon Dioxide 60-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 100-104 21681327-2 2011 Herein, we report the first study for developing mesoporous silica functionalized with phosphonate (NP10) as a sorbent for U(VI) sorption from aqueous solution. Organophosphonates 87-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 100-104 21362629-0 2011 Activation of nuclear TR3 (NR4A1) by a diindolylmethane analog induces apoptosis and proapoptotic genes in pancreatic cancer cells and tumors. 3,3'-diindolylmethane 39-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 22-25 21362629-0 2011 Activation of nuclear TR3 (NR4A1) by a diindolylmethane analog induces apoptosis and proapoptotic genes in pancreatic cancer cells and tumors. 3,3'-diindolylmethane 39-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-32 21362629-1 2011 NR4A1 (Nur77, TR3) is overexpressed in pancreatic tumors and activation of TR3 by 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) inhibits cell and tumor growth and induces apoptosis. 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane 82-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 21362629-1 2011 NR4A1 (Nur77, TR3) is overexpressed in pancreatic tumors and activation of TR3 by 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) inhibits cell and tumor growth and induces apoptosis. 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane 82-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-78 21362629-1 2011 NR4A1 (Nur77, TR3) is overexpressed in pancreatic tumors and activation of TR3 by 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) inhibits cell and tumor growth and induces apoptosis. dim-c-pphoch 130-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 21362629-1 2011 NR4A1 (Nur77, TR3) is overexpressed in pancreatic tumors and activation of TR3 by 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) inhibits cell and tumor growth and induces apoptosis. dim-c-pphoch 130-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 7-12 21362629-1 2011 NR4A1 (Nur77, TR3) is overexpressed in pancreatic tumors and activation of TR3 by 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) inhibits cell and tumor growth and induces apoptosis. dim-c-pphoch 130-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-17 21362629-1 2011 NR4A1 (Nur77, TR3) is overexpressed in pancreatic tumors and activation of TR3 by 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) inhibits cell and tumor growth and induces apoptosis. dim-c-pphoch 130-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-78 21362629-5 2011 Results of this and previous studies demonstrate that TR3 is unique among nuclear receptors since nuclear TR3 is activated or deactivated by diindolylmethane derivatives to induce different apoptotic and growth inhibitory pathways that inhibit pancreatic cancer cell and tumor growth. 3,3'-diindolylmethane 141-157 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-57 21362629-5 2011 Results of this and previous studies demonstrate that TR3 is unique among nuclear receptors since nuclear TR3 is activated or deactivated by diindolylmethane derivatives to induce different apoptotic and growth inhibitory pathways that inhibit pancreatic cancer cell and tumor growth. 3,3'-diindolylmethane 141-157 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-109 21170551-2 2011 METHODS: Patients received exemestane or tamoxifen as adjuvant therapy for hormone receptor-positive breast cancer. Tamoxifen 41-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 21253674-8 2011 Interestingly, MCT-3, MG and AZA alone and in combination increased expression of the novel tumour suppressor gene Nur77, important in leukemogenesis, with MG a more potent inducer as a single agent. Azacitidine 29-32 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-120 20354821-6 2011 HR-negative patients and those whose PS was >= 2, regardless of age, were more likely to choose BSC without chemotherapy. bsc 99-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-2 21109603-4 2011 METHODS AND RESULTS: Whole-genome DNA array hybridization revealed that adenosine induced a set of early genes including the nuclear receptor subfamily 4, group A, member 1 (NR4A1/Nur77/TR3). Adenosine 72-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-172 21380453-1 2011 Acridones carrying an appropriate substituent at N-10 showed significant fluorescence changes on interacting with ATP in HEPES buffer at pH 7.2. Acridones 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-53 21380453-1 2011 Acridones carrying an appropriate substituent at N-10 showed significant fluorescence changes on interacting with ATP in HEPES buffer at pH 7.2. Adenosine Triphosphate 114-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-53 21380453-1 2011 Acridones carrying an appropriate substituent at N-10 showed significant fluorescence changes on interacting with ATP in HEPES buffer at pH 7.2. HEPES 121-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-53 21241664-3 2011 Previously, we have shown that fenretinide-induced apoptosis is Nur77 dependent, and the sensitivity of the cancer cells to fenretinide-induced apoptosis is positively associated with cytoplasmic enrichment of Nur77. Fenretinide 31-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-69 21241664-3 2011 Previously, we have shown that fenretinide-induced apoptosis is Nur77 dependent, and the sensitivity of the cancer cells to fenretinide-induced apoptosis is positively associated with cytoplasmic enrichment of Nur77. Fenretinide 31-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 210-215 21241664-3 2011 Previously, we have shown that fenretinide-induced apoptosis is Nur77 dependent, and the sensitivity of the cancer cells to fenretinide-induced apoptosis is positively associated with cytoplasmic enrichment of Nur77. Fenretinide 124-135 nuclear receptor subfamily 4 group A member 1 Homo sapiens 210-215 21241664-4 2011 The goal of current study was to identify means to modulate nuclear export of Nur77 in order to improve the efficacy of fenretinide. Fenretinide 120-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-83 21241664-9 2011 Fenretinide/PD98059-induced cell death of HepG2 cell was positively associated with induction and cytoplasmic location as well as mitochondria enrichment of Nur77. Fenretinide 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-162 21241664-9 2011 Fenretinide/PD98059-induced cell death of HepG2 cell was positively associated with induction and cytoplasmic location as well as mitochondria enrichment of Nur77. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 12-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-162 21241664-11 2011 Taken together, the current study demonstrates that ERK1/2-modulated Nur77 intracellular location dictates the efficacy of fenretinide-induced apoptosis. Fenretinide 123-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-74 21185724-1 2011 Tamoxifen has a key role in the management of women with hormone receptor (HR) positive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-73 21185724-1 2011 Tamoxifen has a key role in the management of women with hormone receptor (HR) positive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-77 21109603-4 2011 METHODS AND RESULTS: Whole-genome DNA array hybridization revealed that adenosine induced a set of early genes including the nuclear receptor subfamily 4, group A, member 1 (NR4A1/Nur77/TR3). Adenosine 72-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 174-179 21109603-4 2011 METHODS AND RESULTS: Whole-genome DNA array hybridization revealed that adenosine induced a set of early genes including the nuclear receptor subfamily 4, group A, member 1 (NR4A1/Nur77/TR3). Adenosine 72-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 180-185 21109603-4 2011 METHODS AND RESULTS: Whole-genome DNA array hybridization revealed that adenosine induced a set of early genes including the nuclear receptor subfamily 4, group A, member 1 (NR4A1/Nur77/TR3). Adenosine 72-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 186-189 21109603-6 2011 Real-time reverse-transcriptase PCR confirmed that adenosine and its analogue N-ethyl-carboxamidoadenosine elicited a strong induction of NR4A1. Adenosine 51-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 138-143 21109603-6 2011 Real-time reverse-transcriptase PCR confirmed that adenosine and its analogue N-ethyl-carboxamidoadenosine elicited a strong induction of NR4A1. Adenosine-5'-(N-ethylcarboxamide) 78-106 nuclear receptor subfamily 4 group A member 1 Homo sapiens 138-143 21109603-10 2011 Treatment with small interfering RNA directed against NR4A1 attenuated the inhibitory effect of 8CPT on proliferation. 8cpt 96-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-59 21246566-13 2011 The JNK inhibitor, SP600125, inhibited Nur77 mRNA expression and reduced PCH4-induced apoptosis. pyrazolanthrone 19-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 21246566-14 2011 CONCLUSIONS: In conclusion, PCH4, a derivative of BP, induced Nur77-mediated apoptosis via the JNK pathway and this mechanism, which is different from that of BP, may explain the increase in the anti-tumor effects on GBM. butylidenephthalide 50-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 21319187-0 2011 Enrichment of Nur77 mediated by retinoic acid receptor beta leads to apoptosis of human hepatocellular carcinoma cells induced by fenretinide and histone deacetylase inhibitors. Fenretinide 130-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-19 20732932-10 2011 With AP-D, pCR rate was 17.8% for hormone receptor (HR)-negative patients and 15.9% for HR-positive patients. Deuterium 8-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-50 20732932-10 2011 With AP-D, pCR rate was 17.8% for hormone receptor (HR)-negative patients and 15.9% for HR-positive patients. Deuterium 8-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-54 20732932-10 2011 With AP-D, pCR rate was 17.8% for hormone receptor (HR)-negative patients and 15.9% for HR-positive patients. Deuterium 8-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-90 21319187-7 2011 Upon fenretinide and HDACi treatment, the expression of RARbeta and Nur77 were induced and colocalized in the cytosol. Fenretinide 5-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-73 21319187-10 2011 Nur77 was essential for fenretinide-induced and HDACi-induced apoptosis of Huh7 cells. Fenretinide 24-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 21319187-11 2011 Induction of the expression, the interaction, and the nuclear export of RARbeta and Nur77 mediate fenretinide-induced and HDACi-induced apoptosis. Fenretinide 98-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-89 21222496-0 2011 Lapatinib in postmenopausal women with hormone receptor-positive, HER2-positive metastatic breast cancer: profile report. Lapatinib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-55 21383902-6 2011 Results revealed that the new class of 5-deazapteridine and steroid hybrid compounds VIa,b, and d, and the vertical-type bispyridodipyrimidine with n-hexyl chain junction between its N-10 and N-10 atoms Xa, exhibited non-selective PTK binding capacities, with the lowest (Gb). Steroids 60-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 192-196 21383902-6 2011 Results revealed that the new class of 5-deazapteridine and steroid hybrid compounds VIa,b, and d, and the vertical-type bispyridodipyrimidine with n-hexyl chain junction between its N-10 and N-10 atoms Xa, exhibited non-selective PTK binding capacities, with the lowest (Gb). bispyridodipyrimidine 121-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-187 21383902-6 2011 Results revealed that the new class of 5-deazapteridine and steroid hybrid compounds VIa,b, and d, and the vertical-type bispyridodipyrimidine with n-hexyl chain junction between its N-10 and N-10 atoms Xa, exhibited non-selective PTK binding capacities, with the lowest (Gb). bispyridodipyrimidine 121-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 192-196 21383902-6 2011 Results revealed that the new class of 5-deazapteridine and steroid hybrid compounds VIa,b, and d, and the vertical-type bispyridodipyrimidine with n-hexyl chain junction between its N-10 and N-10 atoms Xa, exhibited non-selective PTK binding capacities, with the lowest (Gb). Nitrogen 26-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-187 21383902-6 2011 Results revealed that the new class of 5-deazapteridine and steroid hybrid compounds VIa,b, and d, and the vertical-type bispyridodipyrimidine with n-hexyl chain junction between its N-10 and N-10 atoms Xa, exhibited non-selective PTK binding capacities, with the lowest (Gb). Nitrogen 26-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 192-196 21383902-6 2011 Results revealed that the new class of 5-deazapteridine and steroid hybrid compounds VIa,b, and d, and the vertical-type bispyridodipyrimidine with n-hexyl chain junction between its N-10 and N-10 atoms Xa, exhibited non-selective PTK binding capacities, with the lowest (Gb). dipicrylamine 150-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-187 21383902-6 2011 Results revealed that the new class of 5-deazapteridine and steroid hybrid compounds VIa,b, and d, and the vertical-type bispyridodipyrimidine with n-hexyl chain junction between its N-10 and N-10 atoms Xa, exhibited non-selective PTK binding capacities, with the lowest (Gb). dipicrylamine 150-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 192-196 21146499-4 2011 Nur77 mRNA expression in hESCs was significantly increased after decidualization stimulated by 8-Br-cAMP and medroxyprogesterone acetate (MPA). 8-Bromo Cyclic Adenosine Monophosphate 95-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 20669045-0 2011 Effect of aspirin and other NSAIDs on postmenopausal breast cancer incidence by hormone receptor status: results from a prospective cohort study. Aspirin 10-17 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-96 20669045-1 2011 Aspirin and other non-aspirin non-steroidal anti-inflammatory drugs (NSAIDs) can inhibit aromatase activity and thus could selectively lower incidence of hormone receptor positive tumors. Aspirin 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-170 20669045-1 2011 Aspirin and other non-aspirin non-steroidal anti-inflammatory drugs (NSAIDs) can inhibit aromatase activity and thus could selectively lower incidence of hormone receptor positive tumors. Aspirin 22-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-170 21146499-4 2011 Nur77 mRNA expression in hESCs was significantly increased after decidualization stimulated by 8-Br-cAMP and medroxyprogesterone acetate (MPA). Medroxyprogesterone Acetate 109-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 21146499-4 2011 Nur77 mRNA expression in hESCs was significantly increased after decidualization stimulated by 8-Br-cAMP and medroxyprogesterone acetate (MPA). Medroxyprogesterone Acetate 138-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 21146499-6 2011 Furthermore, knockdown of Nur77 in hESCs significantly decreased decidual PRL promoter activation and substantially attenuated PRL mRNA expression and PRL secretion (P < 0.01) induced by 8-Br-cAMP and MPA. 8-Bromo Cyclic Adenosine Monophosphate 190-199 nuclear receptor subfamily 4 group A member 1 Homo sapiens 26-31 21159167-4 2010 RESULTS: U0126 significantly modulated endogenous expression of several important drug resistance (BCL2, ABCB1, ABCC3), prosurvival (BCL2), DNA repair (BRCA1, BRCA2), hormone receptor (AR, ESR2, PPARgamma) and drug metabolism (CYP3A4) genes newly identified in MM cells. U 0126 9-14 nuclear receptor subfamily 4 group A member 1 Homo sapiens 167-183 20978184-0 2011 PPARgamma-independent thiazolidinedione-mediated inhibition of NUR77 expression in vascular endothelial cells. 2,4-thiazolidinedione 22-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 20978184-3 2011 We have previously reported PPARgamma-independent modulation of NUR77 (also known as Nr4a1), an orphan nuclear receptor deemed important in the atherogenic process, in association with TZD-mediated inhibition of tumour necrosis factor alpha (TNFalpha) induction of plasminogen activator inhibitor type 1 expression. 2,4-thiazolidinedione 185-188 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-69 20978184-3 2011 We have previously reported PPARgamma-independent modulation of NUR77 (also known as Nr4a1), an orphan nuclear receptor deemed important in the atherogenic process, in association with TZD-mediated inhibition of tumour necrosis factor alpha (TNFalpha) induction of plasminogen activator inhibitor type 1 expression. 2,4-thiazolidinedione 185-188 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-90 20978184-4 2011 Here, we report NUR77 mRNA expression is increased in human vascular endothelial cells (HUVEC) stimulated by TNFalpha and that this effect is inhibited by a TZD in a PPARgamma-independent manner. 2,4-thiazolidinedione 157-160 nuclear receptor subfamily 4 group A member 1 Homo sapiens 16-21 20978184-6 2011 TZD treatment also attenuated the binding of nuclear proteins to the nuclear factor kappa B (NF-kappaB)-binding site of the NUR77 promoter in HUVEC in a PPARgamma-independent manner. 2,4-thiazolidinedione 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 124-129 21747904-7 2011 Thus, the presence of ESO Ab identifies a tumor subtype of HR- (HER2- or HER2+) primary BC with frequent ESO expression and, together with the assessment of antigen expression in the tumor, may be instrumental for the selection of patients for whom ESO-based immunotherapy may complement standard therapy. eso ab 22-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-61 21747904-7 2011 Thus, the presence of ESO Ab identifies a tumor subtype of HR- (HER2- or HER2+) primary BC with frequent ESO expression and, together with the assessment of antigen expression in the tumor, may be instrumental for the selection of patients for whom ESO-based immunotherapy may complement standard therapy. Epoxidized soya bean oil 22-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-61 21747904-7 2011 Thus, the presence of ESO Ab identifies a tumor subtype of HR- (HER2- or HER2+) primary BC with frequent ESO expression and, together with the assessment of antigen expression in the tumor, may be instrumental for the selection of patients for whom ESO-based immunotherapy may complement standard therapy. Epoxidized soya bean oil 105-108 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-61 21126059-3 2010 Mechanistic investigations have shown that, upon AKH stimulation, adipokinetic hormone receptor (AKHR) couples to a Gs protein and enhances adenylate cyclase activity, leading to intracellular cAMP accumulation. Cyclic AMP 193-197 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-95 20847229-3 2011 We showed that levels of Nur77 were elevated in a majority of human colon tumors (9/12) compared to their nontumorous tissues and that Nur77 expression could be strongly induced by different colonic carcinogens including deoxycholic acid (DCA). Deoxycholic Acid 221-237 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-30 20847229-3 2011 We showed that levels of Nur77 were elevated in a majority of human colon tumors (9/12) compared to their nontumorous tissues and that Nur77 expression could be strongly induced by different colonic carcinogens including deoxycholic acid (DCA). Deoxycholic Acid 221-237 nuclear receptor subfamily 4 group A member 1 Homo sapiens 135-140 20847229-3 2011 We showed that levels of Nur77 were elevated in a majority of human colon tumors (9/12) compared to their nontumorous tissues and that Nur77 expression could be strongly induced by different colonic carcinogens including deoxycholic acid (DCA). Deoxycholic Acid 239-242 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-30 20847229-3 2011 We showed that levels of Nur77 were elevated in a majority of human colon tumors (9/12) compared to their nontumorous tissues and that Nur77 expression could be strongly induced by different colonic carcinogens including deoxycholic acid (DCA). Deoxycholic Acid 239-242 nuclear receptor subfamily 4 group A member 1 Homo sapiens 135-140 20847229-4 2011 DCA-induced Nur77 expression resulted in up-regulation of antiapoptotic BRE and angiogenic VEGF, and it enhanced the growth, colony formation, and migration of colon cancer cells. Deoxycholic Acid 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-17 20049562-6 2010 Anthracycline era as an independent predictor of OS and DSS was evaluated using Cox proportional hazards models with patient age, hormone receptor status, tumor size, use of radiation therapy, and number of metastatic ALNs as covariates. Anthracyclines 0-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 130-146 21058635-1 2010 In this paper, time-resolved resonance Raman (TR3) spectra of intermediates generated by proton-induced electron-transfer reaction between triplet 2-methoxynaphthalene ((3)ROMe) and decafluorobenzophenone (DFBP) are presented. 2-methoxynaphthalene 147-167 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-49 21058635-1 2010 In this paper, time-resolved resonance Raman (TR3) spectra of intermediates generated by proton-induced electron-transfer reaction between triplet 2-methoxynaphthalene ((3)ROMe) and decafluorobenzophenone (DFBP) are presented. Decafluorobenzophenone 182-204 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-49 21058635-1 2010 In this paper, time-resolved resonance Raman (TR3) spectra of intermediates generated by proton-induced electron-transfer reaction between triplet 2-methoxynaphthalene ((3)ROMe) and decafluorobenzophenone (DFBP) are presented. dfbp 206-210 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-49 21058635-2 2010 The TR3 vibrational spectra and structure of 2-methoxynaphthalene cation radical (ROMe( +)) have been analyzed by density functional theory (DFT) calculation. 2-methoxynaphthalene cation radical 45-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 20977404-4 2010 The results of clinical studies of adjuvant treatment on early-stage hormone-receptor-positive breast-cancer patients under hormonal treatment - especially with the bisphosphonate zoledronic acid - caused excitement because they demonstrated an additive effect on decreasing disease relapses at bone or other sites. Diphosphonates 165-179 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 20829507-0 2010 alpha-Lipoic acid prevents neointimal hyperplasia via induction of p38 mitogen-activated protein kinase/Nur77-mediated apoptosis of vascular smooth muscle cells and accelerates postinjury reendothelialization. Thioctic Acid 0-17 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-109 20829507-3 2010 ALA treatment strongly induced apoptosis of vascular smooth muscle cells and enhanced the expression and cytoplasmic localization of Nur77, which triggers intrinsic apoptotic events. Thioctic Acid 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-138 20829507-4 2010 Small interfering RNA-mediated downregulation of Nur77 diminished this proapoptotic effect of ALA. Thioctic Acid 94-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-54 20829507-5 2010 Moreover, ALA increased p38 mitogen-activated protein kinase phosphorylation, and inhibition of p38 mitogen-activated protein kinase completely blocked ALA-induced vascular smooth muscle cell apoptosis and Nur77 induction and cytoplasmic localization. Thioctic Acid 152-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 206-211 20829507-7 2010 This preventive effect of ALA was significantly reduced by infection of an adenovirus encoding Nur77 small hairpin (sh)RNA. Thioctic Acid 26-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 95-100 20977404-4 2010 The results of clinical studies of adjuvant treatment on early-stage hormone-receptor-positive breast-cancer patients under hormonal treatment - especially with the bisphosphonate zoledronic acid - caused excitement because they demonstrated an additive effect on decreasing disease relapses at bone or other sites. Zoledronic Acid 180-195 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 20977404-9 2010 TAKE HOME MESSAGE: Current evidence supports zoledronic acid as an effective treatment in adjuvant breast-cancer therapy for hormone-receptor-positive breast-cancer patients when added to hormonotherapy. Zoledronic Acid 45-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 20805064-5 2010 A large meta-analysis showed that the addition of a taxane to an anthracycline-based regimen improves outcomes in high-risk patients regardless of age, menopausal status, number of nodes involved, hormone receptor status, and type of taxane. taxane 52-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 197-213 20731528-1 2010 BACKGROUND: The Breast International Group (BIG) 1-98 and Arimidex, Tamoxifen Alone or in Combination (ATAC) trials demonstrated that, in postmenopausal women with hormone receptor positive (HR+) early-stage breast cancer, 5 years of initial adjuvant endocrine therapy with letrozole or anastrozole is superior to tamoxifen. Anastrozole 58-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-180 20731528-1 2010 BACKGROUND: The Breast International Group (BIG) 1-98 and Arimidex, Tamoxifen Alone or in Combination (ATAC) trials demonstrated that, in postmenopausal women with hormone receptor positive (HR+) early-stage breast cancer, 5 years of initial adjuvant endocrine therapy with letrozole or anastrozole is superior to tamoxifen. Tamoxifen 68-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-180 20700120-3 2010 METHODS: We selected patients treated with tamoxifen (40 mg per day) for hormone receptor-positive MBC from whom a blood sample for pharmacogenetic analysis (CYP2D6*3, *4, *5, *6, *10 and *41) was available. Tamoxifen 43-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 73-89 20660371-3 2010 Small interfering RNA-mediated knockdown of TR3 or cell treatment with the TR3 antagonist 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) decreased proliferation, induced apoptosis, and decreased expression of antiapoptotic genes including Bcl-2 and survivin in pancreatic cancer cells. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 90-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-78 20660371-3 2010 Small interfering RNA-mediated knockdown of TR3 or cell treatment with the TR3 antagonist 1,1-bis(3"-indolyl)-1-(p-hydroxyphenyl)methane (DIM-C-pPhOH) decreased proliferation, induced apoptosis, and decreased expression of antiapoptotic genes including Bcl-2 and survivin in pancreatic cancer cells. 1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane 138-149 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-78 20733117-8 2010 In multivariable adjusted analyses, alcohol consumption was positively related to risk of invasive breast cancer overall, invasive lobular carcinoma, and hormone receptor-positive tumors (all P(trend) <= .022). Alcohols 36-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-170 20438716-6 2010 Treatment with a histone deacetylase (HDAC) inhibitor, trichostatin A, also increased Nur77 acetylation. trichostatin A 55-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-91 20438716-10 2010 Finally, the expression of Nur77 increased along with that of p300, but decreased with induction of HDAC1 after treatment with epithelial growth factor, nerve growth factor, or 6-mercaptopurine, suggesting that the self-control of the acetylation status contributes to the transient induction of Nur77 protein. Mercaptopurine 177-193 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-32 20805064-5 2010 A large meta-analysis showed that the addition of a taxane to an anthracycline-based regimen improves outcomes in high-risk patients regardless of age, menopausal status, number of nodes involved, hormone receptor status, and type of taxane. Anthracyclines 65-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 197-213 20682991-0 2010 Combination therapy of 5-fluorouracil with rapamycin for hormone receptor-negative human breast cancer. Fluorouracil 23-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-73 20716898-3 2010 Furthermore, administration of aromatase inhibitor (anastrozole) and trastuzumab was started due to the postoperative pathological diagnosis of hormone receptor-positive and HER2 (score 3+). Anastrozole 52-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-160 20614948-0 2010 Lapatinib: in postmenopausal women with hormone receptor-positive, HER2-positive metastatic breast cancer. Lapatinib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-56 20411565-5 2010 We found that HK434, a PKC agonist, in combination with calcium ionophore, can induce Nur77 and Nor-1 phosphorylation, translocation, Bcl-2 BH3 exposure and thymocyte apoptosis. hk434 14-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-91 20411565-5 2010 We found that HK434, a PKC agonist, in combination with calcium ionophore, can induce Nur77 and Nor-1 phosphorylation, translocation, Bcl-2 BH3 exposure and thymocyte apoptosis. Calcium 56-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-91 20426605-2 2010 Tamoxifen has been the standard adjuvant endocrine therapy for both pre- and post-menopausal women with hormone receptor-positive early breast cancer and remains the standard of care for premenopausal women. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 20410157-0 2010 Assessing hormone receptor activities of pyrethroid insecticides and their metabolites in reporter gene assays. Pyrethrins 41-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-26 20505214-6 2010 A combination of metabolites that increased in plasma in response to exercise (glycerol, niacinamide, glucose-6-phosphate, pantothenate, and succinate) up-regulated the expression of nur77, a transcriptional regulator of glucose utilization and lipid metabolism genes in skeletal muscle in vitro. Glycerol 79-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-188 20505214-6 2010 A combination of metabolites that increased in plasma in response to exercise (glycerol, niacinamide, glucose-6-phosphate, pantothenate, and succinate) up-regulated the expression of nur77, a transcriptional regulator of glucose utilization and lipid metabolism genes in skeletal muscle in vitro. Niacinamide 89-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-188 20505214-6 2010 A combination of metabolites that increased in plasma in response to exercise (glycerol, niacinamide, glucose-6-phosphate, pantothenate, and succinate) up-regulated the expression of nur77, a transcriptional regulator of glucose utilization and lipid metabolism genes in skeletal muscle in vitro. Glucose-6-Phosphate 102-121 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-188 20505214-6 2010 A combination of metabolites that increased in plasma in response to exercise (glycerol, niacinamide, glucose-6-phosphate, pantothenate, and succinate) up-regulated the expression of nur77, a transcriptional regulator of glucose utilization and lipid metabolism genes in skeletal muscle in vitro. Pantothenic Acid 123-135 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-188 20505214-6 2010 A combination of metabolites that increased in plasma in response to exercise (glycerol, niacinamide, glucose-6-phosphate, pantothenate, and succinate) up-regulated the expression of nur77, a transcriptional regulator of glucose utilization and lipid metabolism genes in skeletal muscle in vitro. Succinic Acid 141-150 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-188 20505214-6 2010 A combination of metabolites that increased in plasma in response to exercise (glycerol, niacinamide, glucose-6-phosphate, pantothenate, and succinate) up-regulated the expression of nur77, a transcriptional regulator of glucose utilization and lipid metabolism genes in skeletal muscle in vitro. Glucose 102-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 183-188 20209619-13 2010 Treatment of HR-positive patients with either tamoxifen or toremifene is appropriate. Tamoxifen 46-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-15 20209619-13 2010 Treatment of HR-positive patients with either tamoxifen or toremifene is appropriate. Toremifene 59-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-15 20388790-2 2010 We previously reported that the octaketide cytosporone B (Csn-B) is a natural agonist for Nur77. octaketide cytosporone b 32-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-95 20388790-2 2010 We previously reported that the octaketide cytosporone B (Csn-B) is a natural agonist for Nur77. cytosporone B 58-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-95 20388790-3 2010 In this study, we synthesized a series of Csn-B analogues and performed a structure-activity analysis that suggested criteria for the development of a unique pharmacophore to activate Nur77. cytosporone B 42-47 nuclear receptor subfamily 4 group A member 1 Homo sapiens 184-189 20388790-4 2010 The components of the pharmacophore necessary for binding Nur77 included the benzene ring, the phenolic hydroxyl group, and the acyl chain of the Csn-B scaffold, whereas the key feature for activating the biological function of Nur77 was the ester group. Benzene 77-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-63 20388790-4 2010 The components of the pharmacophore necessary for binding Nur77 included the benzene ring, the phenolic hydroxyl group, and the acyl chain of the Csn-B scaffold, whereas the key feature for activating the biological function of Nur77 was the ester group. Esters 242-247 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-63 20388790-5 2010 Csn-B analogues that bound Nur77 tightly not only stimulated its transactivation activity but also initiated mitochondrial apoptosis by means of novel cross-talk between Nur77 and BRE, an antiapoptotic protein regulated at the transcriptional level. cytosporone B 0-5 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-32 20388790-5 2010 Csn-B analogues that bound Nur77 tightly not only stimulated its transactivation activity but also initiated mitochondrial apoptosis by means of novel cross-talk between Nur77 and BRE, an antiapoptotic protein regulated at the transcriptional level. cytosporone B 0-5 nuclear receptor subfamily 4 group A member 1 Homo sapiens 170-175 19912993-0 2010 Induction and intracellular localization of Nur77 dictate fenretinide-induced apoptosis of human liver cancer cells. Fenretinide 58-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-49 19912993-4 2010 The induction of Nur77 and the cytoplasmic distribution of Nur77 induced by fenretinide were positively correlated with the apoptotic effect of fenretinide in HCC cells. Fenretinide 76-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-22 19912993-4 2010 The induction of Nur77 and the cytoplasmic distribution of Nur77 induced by fenretinide were positively correlated with the apoptotic effect of fenretinide in HCC cells. Fenretinide 76-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-64 19912993-4 2010 The induction of Nur77 and the cytoplasmic distribution of Nur77 induced by fenretinide were positively correlated with the apoptotic effect of fenretinide in HCC cells. Fenretinide 144-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-22 19912993-4 2010 The induction of Nur77 and the cytoplasmic distribution of Nur77 induced by fenretinide were positively correlated with the apoptotic effect of fenretinide in HCC cells. Fenretinide 144-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-64 19912993-6 2010 The intracellular location of Nur77 was also associated with the differential capability of fenretinide-induced ROS generation in these two cell lines. Fenretinide 92-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-35 19912993-6 2010 The intracellular location of Nur77 was also associated with the differential capability of fenretinide-induced ROS generation in these two cell lines. ros 112-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-35 19912993-7 2010 In addition, the knockdown of Nur77 expression by siRNA greatly reduced fenretinide-induced apoptosis and cleaved caspase 3 in Huh-7 cells. Fenretinide 72-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-35 19912993-8 2010 Therefore, our findings demonstrate that fenretinide-induced apoptosis of HCC cells is Nur77 dependent and that the intracellular localization of Nur77 dictates the sensitivity of the HCC cells to fenretinide-induced apoptosis. Fenretinide 41-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-92 19912993-8 2010 Therefore, our findings demonstrate that fenretinide-induced apoptosis of HCC cells is Nur77 dependent and that the intracellular localization of Nur77 dictates the sensitivity of the HCC cells to fenretinide-induced apoptosis. Fenretinide 197-208 nuclear receptor subfamily 4 group A member 1 Homo sapiens 146-151 20096738-0 2010 Involvement of induction and mitochondrial targeting of orphan nuclear receptor Nur77 in 6-OHDA-induced SH-SY5Y cell death. Oxidopamine 89-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-85 20060711-8 2010 Women with hormone-receptor positive tumours, with low levels (-/+/++) of 17HSD1, had a 43% reduced risk of recurrence, when treated with tamoxifen (Hazard Ratio (HR)=0.57; 95% confidence interval (CI), 0.37-0.86; p=0.0086). Tamoxifen 138-147 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-27 20097716-12 2010 In summary, these results suggest that ATF/CREB and NGFI-B family members play a crucial role in the transcriptional regulation of CYP11B2 and adrenal cell capacity to produce aldosterone. Aldosterone 176-187 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-58 20023005-0 2010 Activation of nerve growth factor-induced B alpha by methylene-substituted diindolylmethanes in bladder cancer cells induces apoptosis and inhibits tumor growth. methylene-substituted diindolylmethanes 53-92 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-43 20023005-2 2010 1,1-Bis(3"-indolyl)-1-(p-methoxyphenyl)-methane (DIM-C-pPhOCH(3)) and 1,1-bis(3"-indolyl)-1-(p-phenyl)methane have previously been identified as activators of Nur77, and both compounds inhibited growth and induced apoptosis of UC-5 and KU7 bladder cancer cells. 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)-methane 0-47 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-164 20023005-2 2010 1,1-Bis(3"-indolyl)-1-(p-methoxyphenyl)-methane (DIM-C-pPhOCH(3)) and 1,1-bis(3"-indolyl)-1-(p-phenyl)methane have previously been identified as activators of Nur77, and both compounds inhibited growth and induced apoptosis of UC-5 and KU7 bladder cancer cells. 1,1-bis(3"-indolyl)-1-(p-phenyl)methane 70-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-164 20023005-3 2010 The proapoptotic effects of methylene-substituted diindolylmethanes (C-DIMs) were unaffected by cotreatment with leptomycin B and were dependent on nuclear Nur77, and RNA interference with a small inhibitory RNA for Nur77 (iNur77) demonstrated that C-DIM-induced activation of apoptosis was Nur77-dependent. methylene-substituted diindolylmethanes 28-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 156-161 20023005-3 2010 The proapoptotic effects of methylene-substituted diindolylmethanes (C-DIMs) were unaffected by cotreatment with leptomycin B and were dependent on nuclear Nur77, and RNA interference with a small inhibitory RNA for Nur77 (iNur77) demonstrated that C-DIM-induced activation of apoptosis was Nur77-dependent. methylene-substituted diindolylmethanes 28-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 216-221 20023005-3 2010 The proapoptotic effects of methylene-substituted diindolylmethanes (C-DIMs) were unaffected by cotreatment with leptomycin B and were dependent on nuclear Nur77, and RNA interference with a small inhibitory RNA for Nur77 (iNur77) demonstrated that C-DIM-induced activation of apoptosis was Nur77-dependent. methylene-substituted diindolylmethanes 28-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 216-221 20023005-5 2010 DIM-C-pPhOCH(3) (25 mg/kg/d) also induced apoptosis and inhibited tumor growth in athymic nude mice bearing KU7 cells as xenografts, demonstrating that Nur77-active C-DIMs exhibit potential for bladder cancer chemotherapy by targeting Nur77, which is overexpressed in this tumor type. dim-c-pphoch(3) 0-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 152-157 20023005-5 2010 DIM-C-pPhOCH(3) (25 mg/kg/d) also induced apoptosis and inhibited tumor growth in athymic nude mice bearing KU7 cells as xenografts, demonstrating that Nur77-active C-DIMs exhibit potential for bladder cancer chemotherapy by targeting Nur77, which is overexpressed in this tumor type. dim-c-pphoch(3) 0-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 235-240 20059973-2 2010 Here, we reported the identification of human apolipoprotein A5 (ApoA5), which implicated in lowering plasma triglyceride levels, as a novel target gene of Nur77. Triglycerides 109-121 nuclear receptor subfamily 4 group A member 1 Homo sapiens 156-161 20015449-10 2010 Western blotting revealed that polyethylene combustion products also upregulated several acrolein-responsive protein markers, including GADD45beta, NQO1, HMOX, Hsp70, Nur77 and Egr1. Polyethylene 31-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 167-172 20059973-6 2010 Taken together, our results demonstrated that Nur77 is a novel regulator of human ApoA5 gene expression and provide a new insight into the role of this orphan nuclear receptor in lipoprotein metabolism and triglyceride homeostasis. Triglycerides 206-218 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-51 20890549-0 2010 [Cost-benefit analysis of anastrazol and tamoxifen in adjuvant treatment of hormone receptor-positive, post-menopausal breast cancer]. anastrazol 26-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-92 20890549-15 2010 Therefore, for postmenopausal, early breast cancer hormone receptor positive women in Colombia, the cost-effective alternative is tamoxifen used as adjuvant therapy for five years. Tamoxifen 130-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 19741502-8 2009 HER2-negative, HR-positive ABC patients have a relatively good prognostic after docetaxel-containing first-line therapy. Docetaxel 80-89 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-17 20847826-5 2010 Furthermore, chemotherapy-free regimens (trastuzumab or lapatinib plus aromatase inhibitors) have been identified as additional options for hormone receptor (HR)- and HER2-positive patients. Lapatinib 56-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 140-156 20847826-5 2010 Furthermore, chemotherapy-free regimens (trastuzumab or lapatinib plus aromatase inhibitors) have been identified as additional options for hormone receptor (HR)- and HER2-positive patients. Lapatinib 56-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 158-160 20847831-0 2010 Lapatinib in the Treatment of Hormone Receptor-Positive/ErbB2-Positive Breast Cancer. Lapatinib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-46 20798196-0 2010 Quality of life in hormone receptor-positive HER-2+ metastatic breast cancer patients during treatment with letrozole alone or in combination with lapatinib. Letrozole 108-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-35 20798196-0 2010 Quality of life in hormone receptor-positive HER-2+ metastatic breast cancer patients during treatment with letrozole alone or in combination with lapatinib. Lapatinib 147-156 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-35 19996222-8 2009 CONCLUSIONS: In patients with HR-positive, HER2-normal breast cancer, a population known to have a low incidence of TOP2A gene alterations thought to be predictive of anthracycline benefit, there is a range of TOP2A RNA expression that is strongly associated with recurrence after adjuvant anthracyclines, which provides information complementary to RS, indicating that it merits further evaluation as a prognostic and predictive marker. Anthracyclines 167-180 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-32 19996222-8 2009 CONCLUSIONS: In patients with HR-positive, HER2-normal breast cancer, a population known to have a low incidence of TOP2A gene alterations thought to be predictive of anthracycline benefit, there is a range of TOP2A RNA expression that is strongly associated with recurrence after adjuvant anthracyclines, which provides information complementary to RS, indicating that it merits further evaluation as a prognostic and predictive marker. Anthracyclines 290-304 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-32 19956103-2 2009 Vitamin D deficiency is likely to be one of the many environmental factors influencing T1D development and diagnosis, and, hence, the hormone receptor gene, VDR, was examined for association with T1D risk. Vitamin D 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 134-150 19786658-0 2009 Lapatinib combined with letrozole versus letrozole and placebo as first-line therapy for postmenopausal hormone receptor-positive metastatic breast cancer. Lapatinib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-120 19786658-2 2009 This trial evaluated the effect of adding lapatinib, a dual tyrosine kinase inhibitor blocking epidermal growth factor receptor and human epidermal growth factor receptor 2 (HER2), to the aromatase inhibitor letrozole as first-line treatment of hormone receptor (HR) -positive metastatic breast cancer (MBC). Lapatinib 42-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 245-261 19553291-0 2009 Gefitinib treatment in hormone-resistant and hormone receptor-negative advanced breast cancer. Gefitinib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-61 19553291-2 2009 Gefinitib is an orally active selective EGFR inhibitor which might benefit advanced breast cancer (ABC) patients either with acquired hormone resistance or with hormone receptor (HR)-negative tumors. gefinitib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 161-177 19553291-2 2009 Gefinitib is an orally active selective EGFR inhibitor which might benefit advanced breast cancer (ABC) patients either with acquired hormone resistance or with hormone receptor (HR)-negative tumors. gefinitib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 179-181 19731013-0 2010 A randomized trial exploring the biomarker effects of neoadjuvant sequential treatment with exemestane and anastrozole in post-menopausal women with hormone receptor-positive breast cancer. exemestane 93-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 151-168 19731013-0 2010 A randomized trial exploring the biomarker effects of neoadjuvant sequential treatment with exemestane and anastrozole in post-menopausal women with hormone receptor-positive breast cancer. Anastrozole 109-120 nuclear receptor subfamily 4 group A member 1 Homo sapiens 151-168 20043345-0 2010 Fractionated evaluation of immunohistochemical hormone receptor expression enhances prognostic prediction in breast cancer patients treated with tamoxifen as adjuvant therapy. Tamoxifen 145-154 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-63 20156908-0 2010 Lapatinib plus letrozole as first-line therapy for HER-2+ hormone receptor-positive metastatic breast cancer. Lapatinib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 58-74 20156908-1 2010 OBJECTIVE: To evaluate the efficacy and tolerability of letrozole plus lapatinib versus letrozole plus placebo in women with hormone receptor (HR)(+) human epidermal growth factor receptor (HER)-2(+) tumors receiving first-line therapy for metastatic breast cancer (MBC). Letrozole 56-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 20156908-1 2010 OBJECTIVE: To evaluate the efficacy and tolerability of letrozole plus lapatinib versus letrozole plus placebo in women with hormone receptor (HR)(+) human epidermal growth factor receptor (HER)-2(+) tumors receiving first-line therapy for metastatic breast cancer (MBC). Lapatinib 71-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 20389141-1 2010 BACKGROUND: In the "Arimidex", Tamoxifen Alone or in Combination (ATAC) trial, the aromatase inhibitor (AI) anastrozole had a significantly better efficacy and safety profile than tamoxifen as initial adjuvant therapy for hormone receptor-positive (HR+) early breast cancer (EBC) in postmenopausal patients. Anastrozole 108-119 nuclear receptor subfamily 4 group A member 1 Homo sapiens 222-239 19751824-0 2009 ROS inhibit the expression of testicular steroidogenic enzyme genes via the suppression of Nur77 transactivation. Reactive Oxygen Species 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-96 19751824-3 2009 Here, we investigated the effects of ROS on the transcriptional activity of Nur77, one of the major transcription factors that regulate the expression of steroidogenic enzyme genes. Reactive Oxygen Species 37-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-81 19751824-4 2009 ROS signaling inhibited Nur77 transactivation, which was diminished by either treatment with c-Jun N-terminal kinase (JNK) inhibitor or the expression of a dominant negative form of JNK. Reactive Oxygen Species 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 24-29 19751824-9 2009 Together, these results suggest that ROS signaling-mediated c-Jun upregulation suppresses the expression of steroidogenic enzyme genes by inhibiting Nur77 transactivation, resulting in the reduction of testicular steroidogenesis. Reactive Oxygen Species 37-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-154 19786670-9 2009 CONCLUSION: Trastuzumab plus anastrozole improves outcomes for patients with HER2/hormone receptor-copositive MBC compared with anastrozole alone, although adverse events and serious adverse events were more frequent with the combination. Anastrozole 29-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-98 19809429-1 2009 BACKGROUND: To evaluate the impact of change in the hormone receptor (HR) status (HR status conversion) on the long-term outcomes of breast cancer patients treated with neoadjuvant chemotherapy (NAC). nac 195-198 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-68 19809429-1 2009 BACKGROUND: To evaluate the impact of change in the hormone receptor (HR) status (HR status conversion) on the long-term outcomes of breast cancer patients treated with neoadjuvant chemotherapy (NAC). nac 195-198 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-72 19809429-1 2009 BACKGROUND: To evaluate the impact of change in the hormone receptor (HR) status (HR status conversion) on the long-term outcomes of breast cancer patients treated with neoadjuvant chemotherapy (NAC). nac 195-198 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-84 19619604-4 2009 In this study we report the antibacterial properties of a peptide (AVWQFRKMIK-CONH(2); N10 peptide), which corresponds to the N-terminal first ten amino acid residues of hp-sPLA(2), against E. coli. hp-spla 170-177 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-90 19838061-1 2009 Tetraiodothyroacetic acid (tetrac) inhibits the cellular actions of thyroid hormone initiated at the hormone receptor on plasma membrane integrin alphavbeta3. tetraiodothyroacetic acid 0-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 101-117 19838061-1 2009 Tetraiodothyroacetic acid (tetrac) inhibits the cellular actions of thyroid hormone initiated at the hormone receptor on plasma membrane integrin alphavbeta3. tetraiodothyroacetic acid 27-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 101-117 19809024-1 2009 CONTEXT: The growth inhibitory effect of tamoxifen, which is used for the treatment of hormone receptor-positive breast cancer, is mediated by its metabolites, 4-hydroxytamoxifen and endoxifen. Tamoxifen 41-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-103 19897535-10 2009 Patients with HR(-) tumors had significantly lower 10-year DFS (17.3% versus 46.4%; p = .018) and OS (17.3% versus 70.2%; p = .002) rates. Osmium 98-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-16 19809024-1 2009 CONTEXT: The growth inhibitory effect of tamoxifen, which is used for the treatment of hormone receptor-positive breast cancer, is mediated by its metabolites, 4-hydroxytamoxifen and endoxifen. hydroxytamoxifen 160-178 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-103 19809024-1 2009 CONTEXT: The growth inhibitory effect of tamoxifen, which is used for the treatment of hormone receptor-positive breast cancer, is mediated by its metabolites, 4-hydroxytamoxifen and endoxifen. 4-hydroxy-N-desmethyltamoxifen 183-192 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-103 19671798-0 2009 Paclitaxel directly binds to Bcl-2 and functionally mimics activity of Nur77. Paclitaxel 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-76 19738041-0 2009 Structural basis for the inhibition of human 5,10-methenyltetrahydrofolate synthetase by N10-substituted folate analogues. Folic Acid 68-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-92 19738041-6 2009 Binding of N10-substituted folate analogues places Y152 in the middle of the channel connecting ATP binding site with the substrate binding pocket, precluding the positioning of gamma-phosphate for a nucleophilic attack. Folic Acid 27-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-14 19738041-6 2009 Binding of N10-substituted folate analogues places Y152 in the middle of the channel connecting ATP binding site with the substrate binding pocket, precluding the positioning of gamma-phosphate for a nucleophilic attack. Adenosine Triphosphate 96-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-14 19738041-6 2009 Binding of N10-substituted folate analogues places Y152 in the middle of the channel connecting ATP binding site with the substrate binding pocket, precluding the positioning of gamma-phosphate for a nucleophilic attack. gamma-phosphate 178-193 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-14 19635563-0 2009 Nur77 mRNA levels and L-Dopa-induced dyskinesias in MPTP monkeys treated with docosahexaenoic acid. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine 52-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 19635563-0 2009 Nur77 mRNA levels and L-Dopa-induced dyskinesias in MPTP monkeys treated with docosahexaenoic acid. Docosahexaenoic Acids 78-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 19635563-6 2009 On the other hand, denervation reduced Nur77 mRNA levels, whereas chronic L-Dopa treatment strongly induced Nur77 transcripts. Levodopa 74-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-113 19635563-8 2009 Interestingly, combination of L-Dopa with DHA further increases Nur77 mRNA levels in the anterior caudate-putamen, and mainly in striosomes. Levodopa 30-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-69 19635563-8 2009 Interestingly, combination of L-Dopa with DHA further increases Nur77 mRNA levels in the anterior caudate-putamen, and mainly in striosomes. Docosahexaenoic Acids 42-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-69 19635563-10 2009 Taken together, our results show that Nur77 expression is modulated following dopamine denervation and chronic L-Dopa therapy in a non-human primate model of Parkinson"s disease, and suggest that strong modulation of Nur77 expression might be linked to a reduced risk to develop LIDs. Dopamine 78-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 19635563-10 2009 Taken together, our results show that Nur77 expression is modulated following dopamine denervation and chronic L-Dopa therapy in a non-human primate model of Parkinson"s disease, and suggest that strong modulation of Nur77 expression might be linked to a reduced risk to develop LIDs. Levodopa 111-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 19671798-4 2009 We tested the hypothesis that paclitaxel mimics Nur77, which, like paclitaxel, changes the function of Bcl-2. Paclitaxel 30-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 19671798-4 2009 We tested the hypothesis that paclitaxel mimics Nur77, which, like paclitaxel, changes the function of Bcl-2. Paclitaxel 67-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 19671798-5 2009 This premise was confirmed by Nur77 interacting with both paclitaxel targets (Bcl-2 and beta-tubulin) and a peptide sequence mimicking the Nur77 structural region, thus reproducing the paclitaxel-like effects of tubulin polymerization and opening the permeability transition pore channel in mitochondria. Paclitaxel 58-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-35 19671798-5 2009 This premise was confirmed by Nur77 interacting with both paclitaxel targets (Bcl-2 and beta-tubulin) and a peptide sequence mimicking the Nur77 structural region, thus reproducing the paclitaxel-like effects of tubulin polymerization and opening the permeability transition pore channel in mitochondria. Paclitaxel 185-195 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-35 19671798-5 2009 This premise was confirmed by Nur77 interacting with both paclitaxel targets (Bcl-2 and beta-tubulin) and a peptide sequence mimicking the Nur77 structural region, thus reproducing the paclitaxel-like effects of tubulin polymerization and opening the permeability transition pore channel in mitochondria. Paclitaxel 185-195 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 19682370-1 2009 BACKGROUND: Neuron-derived orphan receptor (Nor) 1, nuclear receptor (Nur) 77, and nuclear receptor-related protein (Nurr) 1 constitute the NR4A family of orphan nuclear receptors which were recently found to modulate hepatic glucose production, insulin signalling in adipocytes, and oxidative metabolism in skeletal muscle. Glucose 226-233 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-77 19675165-5 2009 Specifically, we demonstrate that RSK phosphorylates Nur77 at serine 354 and this modulates Nur77 nuclear export and intracellular translocation during T cell death. Serine 62-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-58 19675165-5 2009 Specifically, we demonstrate that RSK phosphorylates Nur77 at serine 354 and this modulates Nur77 nuclear export and intracellular translocation during T cell death. Serine 62-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-97 19690310-2 2009 OBJECTIVE: To determine whether 6 mg of estradiol (daily) is a viable therapy for postmenopausal women with advanced aromatase inhibitor-resistant hormone receptor-positive breast cancer. Estradiol 40-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 147-163 19378296-1 2009 PPARgamma agonist DIM-Ph-4-CF(3), a template for RXRalpha agonist (E)-3-[5-di(1-methyl-1H-indol-3-yl)methyl-2-thienyl] acrylic acid: DIM-Ph-CF(3) is reported to inhibit cancer growth independent of PPARgamma and to interact with NR4A1. dim-ph-4-cf 18-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 229-234 19541862-0 2009 Understanding resistance to tamoxifen in hormone receptor-positive breast cancer. Tamoxifen 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-57 19121891-5 2009 In this work, five surfactants, namely Brij 35, Tergitol NP10, Tween 20, Tween 80 and Tyloxapol, are evaluated on the desorption of PAHs [benzanthracene (BzA), fluoranthene (FLU), and pyrene (PYR), single and in mixture] from a model sample such as kaolin. Polycyclic Aromatic Hydrocarbons 132-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-61 19378296-1 2009 PPARgamma agonist DIM-Ph-4-CF(3), a template for RXRalpha agonist (E)-3-[5-di(1-methyl-1H-indol-3-yl)methyl-2-thienyl] acrylic acid: DIM-Ph-CF(3) is reported to inhibit cancer growth independent of PPARgamma and to interact with NR4A1. (e)-3-[5-di(1-methyl-1h-indol-3-yl)methyl-2-thienyl] acrylic acid 66-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 229-234 19378296-1 2009 PPARgamma agonist DIM-Ph-4-CF(3), a template for RXRalpha agonist (E)-3-[5-di(1-methyl-1H-indol-3-yl)methyl-2-thienyl] acrylic acid: DIM-Ph-CF(3) is reported to inhibit cancer growth independent of PPARgamma and to interact with NR4A1. dim-ph 18-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 229-234 19378296-4 2009 Structure-based direct design led to an RXRalpha agonist.1-Di(1H-indol-3-yl)methyl-4-trifluoromethylbenzene (DIM-Ph-4-CF(3)) is reported to inhibit cancer cell growth and to act as a transcriptional agonist of peroxisome proliferator-activated receptor gamma (PPARgamma) and nuclear receptor 4A subfamily member 1 (NR4A1). 1-di(1h-indol-3-yl)methyl-4-trifluoromethylbenzene 57-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 275-313 19378296-4 2009 Structure-based direct design led to an RXRalpha agonist.1-Di(1H-indol-3-yl)methyl-4-trifluoromethylbenzene (DIM-Ph-4-CF(3)) is reported to inhibit cancer cell growth and to act as a transcriptional agonist of peroxisome proliferator-activated receptor gamma (PPARgamma) and nuclear receptor 4A subfamily member 1 (NR4A1). 1-di(1h-indol-3-yl)methyl-4-trifluoromethylbenzene 57-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 315-320 21783983-8 2009 Of these, rapid and transient induction of the TR3 gene was noted as a possible key process in Cd-induced apoptosis. Cadmium 95-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-50 19451417-0 2009 Metronomic schedule of paclitaxel is effective in hormone receptor-positive and hormone receptor-negative breast cancer. Paclitaxel 23-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-66 19473021-1 2009 Time-resolved resonance Raman spectroscopy (TR3) has been used to study the effect of solvent polarity on the mechanism and nature of intermediates formed in photoinduced electron-transfer reaction between triplet flouranil ((3)FL) and tetramethylbenzene (TMB). triplet flouranil 206-223 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-47 19473021-1 2009 Time-resolved resonance Raman spectroscopy (TR3) has been used to study the effect of solvent polarity on the mechanism and nature of intermediates formed in photoinduced electron-transfer reaction between triplet flouranil ((3)FL) and tetramethylbenzene (TMB). 1,2,3,4-TETRAMETHYLBENZENE 236-254 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-47 19473021-1 2009 Time-resolved resonance Raman spectroscopy (TR3) has been used to study the effect of solvent polarity on the mechanism and nature of intermediates formed in photoinduced electron-transfer reaction between triplet flouranil ((3)FL) and tetramethylbenzene (TMB). 1,2,4,5-tetramethoxybenzene 256-259 nuclear receptor subfamily 4 group A member 1 Homo sapiens 44-47 19473021-2 2009 Comparison of the TR3 spectra in polar, nonpolar, and medium polar media suggests that formation of radical anion due to electron-transfer reaction between (3)FL and TMB is favored in more polar solvents, whereas ketyl radical formation is more favored in less polar media. (3)fl 156-161 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-21 19473021-2 2009 Comparison of the TR3 spectra in polar, nonpolar, and medium polar media suggests that formation of radical anion due to electron-transfer reaction between (3)FL and TMB is favored in more polar solvents, whereas ketyl radical formation is more favored in less polar media. 1,2,4,5-tetramethoxybenzene 166-169 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-21 19473021-2 2009 Comparison of the TR3 spectra in polar, nonpolar, and medium polar media suggests that formation of radical anion due to electron-transfer reaction between (3)FL and TMB is favored in more polar solvents, whereas ketyl radical formation is more favored in less polar media. ketyl radical 213-226 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-21 19584258-1 2009 1,1-Bis(3"-indolyl)-1-(p-anisyl)methane (DIM-C-pPhOCH3) activates the orphan receptor nerve growth factor-induced Balpha (Nur77) in cancer cells, and in this study, DIM-C-pPhOCH3 decreased Panc1 pancreatic cancer cell survival and arrested cells in G0-G1. 1,1-bis(3'-indolyl)-1-(p-anisyl)methane 0-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-127 19584258-1 2009 1,1-Bis(3"-indolyl)-1-(p-anisyl)methane (DIM-C-pPhOCH3) activates the orphan receptor nerve growth factor-induced Balpha (Nur77) in cancer cells, and in this study, DIM-C-pPhOCH3 decreased Panc1 pancreatic cancer cell survival and arrested cells in G0-G1. DIM-C-pPhOCH3 41-54 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-127 19584258-5 2009 Interactions of Nur77 with the p21 promoter in Panc1 cells treated with DIM-C-pPhOCH3 were also confirmed in chromatin immunoprecipitation assays. DIM-C-pPhOCH3 72-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 16-21 19451417-0 2009 Metronomic schedule of paclitaxel is effective in hormone receptor-positive and hormone receptor-negative breast cancer. Paclitaxel 23-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-96 19074726-4 2009 Here, we demonstrate that treatment with panobinostat rapidly inhibits the in vitro and intracellular activity, as well as the mRNA and protein levels of HDAC7, and induces expression and translocation of Nur77 to the mitochondria. Panobinostat 41-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 205-210 19436228-2 2009 Treatment with thapsigargin in the presence of blockers of NMDA (N-methyl-D-aspartic acid) receptors upregulates some activity-dependent genes (Egr2 and Nr4a1), leaving unaltered the expression level of other activity-dependent genes (Bdnf and Arc). Thapsigargin 15-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-158 19454038-0 2009 Potential antitumor effects of nitrogen-containing bisphosphonate in hormone receptor negative breast cancer patients with bone metastases. Nitrogen 31-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-85 19454038-1 2009 BACKGROUND: This retrospective study evaluated, according to hormone receptor status, the antitumor effects of bisphosphonate especially on survival and disease progression in breast cancer patients with metastatic bone disease. Diphosphonates 111-125 nuclear receptor subfamily 4 group A member 1 Homo sapiens 61-77 19454038-4 2009 RESULTS: 87.8% of HR positive and 69.0% of HR negative patients received BPs with a median number of 17.7 cycles. Diphosphonates 73-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-45 19454038-5 2009 Although BPs treatment made no survival benefit in HR positive group, HR negative patients showed a significant prolonged survival when they received BPs treatment (hazard ratio = 0.56 [95% CI 0.34 to 0.91], P = 0.019). Diphosphonates 150-153 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-72 19454038-7 2009 CONCLUSION: Bisphosphonate treatment can result in a survival benefit in metastatic breast cancer patients with HR negative tumors. Diphosphonates 12-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-114 19153124-1 2009 BACKGROUND: Fulvestrant produces a clinical benefit rate (CBR) of approximately 45% in tamoxifen-resistant, hormone receptor (HR)-positive metastatic breast cancer (MBC) and 32% in aromatase inhibitor (AI)-resistant disease. Fulvestrant 12-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-124 19153124-1 2009 BACKGROUND: Fulvestrant produces a clinical benefit rate (CBR) of approximately 45% in tamoxifen-resistant, hormone receptor (HR)-positive metastatic breast cancer (MBC) and 32% in aromatase inhibitor (AI)-resistant disease. Fulvestrant 12-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-128 19416189-8 2009 Testosterone responsiveness was found to be mediated through an element located in the proximal INSL3 promoter, which also contains a NUR77-SF1-binding site. Testosterone 0-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 134-139 19153124-3 2009 The objective of this study was to determine the efficacy and safety of tipifarnib-fulvestrant combination in HR-positive MBC. tipifarnib-fulvestrant 72-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-112 19136619-6 2009 Taken together, these observations indicate that liraglutide inhibits TNF- or glucose-mediated induction of PAI-1 and vascular adhesion molecule expression, and this effect may involve the modulation of NUR77. Glucose 78-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 203-208 19153124-10 2009 CONCLUSIONS: The target CBR of 70% for the tipifarnib-fulvestrant combination in HR-positive MBC was set too high and was not achieved. tipifarnib-fulvestrant 43-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-83 18954499-2 2008 For over 20 years, tamoxifen was the standard adjuvant (postoperative) endocrine treatment for hormone receptor-positive (i.e., endocrine-responsive) early breast cancer. Tamoxifen 19-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 95-111 19243953-1 2009 By combining the structural features of acridone based anti-cancer drugs (like amsacrine) and MDR modulator propafenone, acridones with hydroxyl amine chain at N-10 have been designed and synthesized. Propafenone 108-119 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-164 19243953-1 2009 By combining the structural features of acridone based anti-cancer drugs (like amsacrine) and MDR modulator propafenone, acridones with hydroxyl amine chain at N-10 have been designed and synthesized. Acridones 121-130 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-164 19243953-1 2009 By combining the structural features of acridone based anti-cancer drugs (like amsacrine) and MDR modulator propafenone, acridones with hydroxyl amine chain at N-10 have been designed and synthesized. Hydroxylamine 136-150 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-164 18727708-0 2009 Down-regulation of NR4A1 in follicular thyroid carcinomas is restored following lithium treatment. Lithium 80-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-24 18727708-4 2009 NR4A1 can be transiently increased by a variety of stimuli, including lithium, which is used as adjuvant therapy of thyroid carcinoma with (131)I. Lithium 70-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 18727708-5 2009 We tested if lithium could restore NR4A1 expression. Lithium 13-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-40 18727708-11 2009 Lithium induced NR4A1 and FOSB expression, reduced CCDN1 expression, inhibited cell growth and triggered apoptosis in a FTC cell line. Lithium 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 16-21 18727708-15 2009 Lithium restores NR4A1 expression, induces apoptosis and reduces cell growth. Lithium 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-22 20198292-7 2009 In fact, retrospective analyses of clinical trials suggest that anthracyclines may be less active in hormone-receptor positive HER2-negative patients, while several other trials and meta-analyses involving taxanes, showed a benefit in terms of risk of relapse and death reduction. Anthracyclines 64-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 101-117 20198292-11 2009 Nevertheless, the addition of taxanes, mainly docetaxel, to anthracyclines, seems to overcome the relative chemoresistance of hormone-receptor positive tumors, providing a benefit in disease free survival and overall survival. Taxoids 30-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 20198292-11 2009 Nevertheless, the addition of taxanes, mainly docetaxel, to anthracyclines, seems to overcome the relative chemoresistance of hormone-receptor positive tumors, providing a benefit in disease free survival and overall survival. Docetaxel 46-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 20198292-11 2009 Nevertheless, the addition of taxanes, mainly docetaxel, to anthracyclines, seems to overcome the relative chemoresistance of hormone-receptor positive tumors, providing a benefit in disease free survival and overall survival. Anthracyclines 60-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 19148494-0 2009 The anti-leukemic effect of a novel histone deacetylase inhibitor MCT-1 and 5-aza-cytidine involves augmentation of Nur77 and inhibition of MMP-9 expression. Azacitidine 76-90 nuclear receptor subfamily 4 group A member 1 Homo sapiens 116-121 19148494-4 2009 Interestingly, MCT-1 in combination with AZA significantly induced the recently identified suppressor of leukemogenesis Nur77 and attenuated AZA-induced MMP-9 expression. Azacitidine 41-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-125 18501502-7 2008 For example, p-trifluoromethylphenyl, p-t-butylphenyl and p-biphenyl analogs activate peroxisome proliferator-activated receptor gamma (PPARgamma), and p-methoxyphenyl and p-phenyl compounds activate nerve growth factor-induced-Balpha (NGFI-Balpha, Nur77) orphan nuclear receptor. phenyl compounds 174-190 nuclear receptor subfamily 4 group A member 1 Homo sapiens 249-254 18158620-0 2008 Exemestane as primary systemic treatment for hormone receptor positive post-menopausal breast cancer patients: a phase II trial of the Austrian Breast and Colorectal Cancer Study Group (ABCSG-17). exemestane 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-61 18158620-9 2008 CONCLUSION: This study shows that exemestane is effective and safe as a preoperative therapy in post-menopausal patients with strongly hormone receptor-positive breast cancer. exemestane 34-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 135-151 19046107-1 2008 A 5-year regimen of tamoxifen hormone therapy has historically been the recommendation for hormone receptor-positive, postmenopausal women with early-stage breast cancer. Tamoxifen 20-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-107 18756015-0 2008 Vitamin D from dietary intake and sunlight exposure and the risk of hormone-receptor-defined breast cancer. vitamin d 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-84 18756015-1 2008 Evidence has emerged for a role of vitamin D in the development of breast cancer, and there is some suggestion that its antiproliferative effect is greater in hormone-receptor-positive cells. vitamin d 35-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-175 18501502-8 2008 The effects of C-DIMs on PPARgamma and Nur77 coupled with their receptor-independent activities has resulted in the development of a novel group of multi-targeted anticancer drugs with excellent potential for clinical treatment of cancer. c-dims 15-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 18490163-3 2008 The aromatase inhibitors (anastrozole, letrozole, and exemestane) have been shown to be superior to tamoxifen in improving disease-free survival in postmenopausal women with hormone receptor-positive breast cancer. Anastrozole 26-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 174-190 18676081-5 2008 Our results show that NGFI-B LBD undergoes a two-state guanidine hydrochloride (GndHCl) induced denaturation, as judged by changes in the alpha-helical content of the protein monitored by circular dichroism spectroscopy (CD). Guanidine 55-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 22-28 18676081-5 2008 Our results show that NGFI-B LBD undergoes a two-state guanidine hydrochloride (GndHCl) induced denaturation, as judged by changes in the alpha-helical content of the protein monitored by circular dichroism spectroscopy (CD). Guanidine 80-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 22-28 18852139-1 2008 1,1-Bis(3"-indoly)-1-(p-substituted phenyl)methanes (C-DIM) exhibit structure-dependent activation of peroxisome proliferator-activated receptor gamma and nerve growth factor-induced Balpha (Nur77) and induce receptor-dependent and receptor-independent apoptosis in cancer cells and tumors. 1,1-bis(3"-indoly)-1-(p-substituted phenyl)methanes 0-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 191-196 18599618-5 2008 We have now established that StAR transcription in cAMP-stimulated Leydig cells requires de novo protein synthesis and involves NUR77. Cyclic AMP 51-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 128-133 18599618-6 2008 We found that cAMP-induced NUR77 expression precedes that of StAR both at the mRNA and protein levels in Leydig cells. Cyclic AMP 14-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-32 18599618-7 2008 In these cells, small interfering RNA-mediated NUR77 knockdown reduces cAMP-induced StAR expression. Cyclic AMP 71-75 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-52 18599618-12 2008 All together, our results implicate NUR77 as a mediator of cAMP action on StAR transcription in steroidogenic Leydig cells and identify a role for CaMKI in this process. Cyclic AMP 59-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 36-41 18490163-3 2008 The aromatase inhibitors (anastrozole, letrozole, and exemestane) have been shown to be superior to tamoxifen in improving disease-free survival in postmenopausal women with hormone receptor-positive breast cancer. Letrozole 39-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 174-190 18490163-3 2008 The aromatase inhibitors (anastrozole, letrozole, and exemestane) have been shown to be superior to tamoxifen in improving disease-free survival in postmenopausal women with hormone receptor-positive breast cancer. exemestane 54-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 174-190 18075758-0 2008 Histopathological assessment of anastrozole and tamoxifen as preoperative (neoadjuvant) treatment in postmenopausal Japanese women with hormone receptor-positive breast cancer in the PROACT trial. Anastrozole 32-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 136-152 18626112-1 2008 Nuclear receptor TR3/Nur77/NR4A1 binds several antiapoptotic Bcl-2-family proteins (Bcl-B, Bcl-2, Bfl-1) in a non-BH3-dependent manner. BH 3 114-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-20 18626112-1 2008 Nuclear receptor TR3/Nur77/NR4A1 binds several antiapoptotic Bcl-2-family proteins (Bcl-B, Bcl-2, Bfl-1) in a non-BH3-dependent manner. BH 3 114-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 21-26 18626112-1 2008 Nuclear receptor TR3/Nur77/NR4A1 binds several antiapoptotic Bcl-2-family proteins (Bcl-B, Bcl-2, Bfl-1) in a non-BH3-dependent manner. BH 3 114-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-32 18626112-2 2008 A 9-amino-acid peptide derived from full-length TR3 with polyarginine tail (TR3-r8) recapitulates TR3"s binding specificity, displaying high affinity for Bcl-B. polyarginine 57-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-51 18626112-2 2008 A 9-amino-acid peptide derived from full-length TR3 with polyarginine tail (TR3-r8) recapitulates TR3"s binding specificity, displaying high affinity for Bcl-B. polyarginine 57-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-79 18626112-2 2008 A 9-amino-acid peptide derived from full-length TR3 with polyarginine tail (TR3-r8) recapitulates TR3"s binding specificity, displaying high affinity for Bcl-B. polyarginine 57-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-79 18626112-4 2008 A fluorescence polarization assay (FPA) employing fluorescein isothiocyanate (FITC)-labeled TR3-r8 peptide (FITC-TR3-r8) and Bcl-B protein was optimized, with nonfluorescent TR3-r8 serving to demonstrate reversible, competitive binding. Fluorescein-5-isothiocyanate 50-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-95 18626112-4 2008 A fluorescence polarization assay (FPA) employing fluorescein isothiocyanate (FITC)-labeled TR3-r8 peptide (FITC-TR3-r8) and Bcl-B protein was optimized, with nonfluorescent TR3-r8 serving to demonstrate reversible, competitive binding. Fluorescein-5-isothiocyanate 50-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-116 18626112-4 2008 A fluorescence polarization assay (FPA) employing fluorescein isothiocyanate (FITC)-labeled TR3-r8 peptide (FITC-TR3-r8) and Bcl-B protein was optimized, with nonfluorescent TR3-r8 serving to demonstrate reversible, competitive binding. Fluorescein-5-isothiocyanate 50-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-116 18626112-4 2008 A fluorescence polarization assay (FPA) employing fluorescein isothiocyanate (FITC)-labeled TR3-r8 peptide (FITC-TR3-r8) and Bcl-B protein was optimized, with nonfluorescent TR3-r8 serving to demonstrate reversible, competitive binding. Fluorescein-5-isothiocyanate 78-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-95 18626112-5 2008 Approximately 50,000 compounds were screened at 3.75 mg/L, yielding 145 reproducible hits with > or =50% FITC-TR3-r8 displacement (a confirmed hit rate of 0.29%). Fluorescein-5-isothiocyanate 108-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-116 18419761-6 2008 After BP treatment in GBM 8401 cells, Nur77 translocated from the nucleus to the cytoplasm, the cytochrome c was released from the mitochondria, and caspase 3 became activated. butylidenephthalide 6-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 18419761-8 2008 Inhibition of BP-induced Nur77 expression by Nur77 short interfering RNA blocked BP-induced apoptosis in GBM 8401 cells, suggesting that the induction of Nur77 negatively affected GBM 8401 cell survival. butylidenephthalide 14-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-30 18419761-8 2008 Inhibition of BP-induced Nur77 expression by Nur77 short interfering RNA blocked BP-induced apoptosis in GBM 8401 cells, suggesting that the induction of Nur77 negatively affected GBM 8401 cell survival. butylidenephthalide 14-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-50 18419761-8 2008 Inhibition of BP-induced Nur77 expression by Nur77 short interfering RNA blocked BP-induced apoptosis in GBM 8401 cells, suggesting that the induction of Nur77 negatively affected GBM 8401 cell survival. butylidenephthalide 14-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-50 18419761-8 2008 Inhibition of BP-induced Nur77 expression by Nur77 short interfering RNA blocked BP-induced apoptosis in GBM 8401 cells, suggesting that the induction of Nur77 negatively affected GBM 8401 cell survival. butylidenephthalide 81-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-30 18419761-8 2008 Inhibition of BP-induced Nur77 expression by Nur77 short interfering RNA blocked BP-induced apoptosis in GBM 8401 cells, suggesting that the induction of Nur77 negatively affected GBM 8401 cell survival. butylidenephthalide 81-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-50 18419761-8 2008 Inhibition of BP-induced Nur77 expression by Nur77 short interfering RNA blocked BP-induced apoptosis in GBM 8401 cells, suggesting that the induction of Nur77 negatively affected GBM 8401 cell survival. butylidenephthalide 81-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-50 18419761-9 2008 In summary, our results suggest that up-regulation of Nur77 may explain the antitumoral activity of BP in brain tumor cells. butylidenephthalide 100-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-59 18424253-3 2008 Glucocorticoid hormone receptor (GR) was translocated from the cytoplasm to the nucleus and de-phosphorylated at serine residue 203 in the nucleus, by combined treatment with dexamethasone and PD98059. Serine 113-119 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-31 18424253-3 2008 Glucocorticoid hormone receptor (GR) was translocated from the cytoplasm to the nucleus and de-phosphorylated at serine residue 203 in the nucleus, by combined treatment with dexamethasone and PD98059. Dexamethasone 175-188 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-31 18424253-3 2008 Glucocorticoid hormone receptor (GR) was translocated from the cytoplasm to the nucleus and de-phosphorylated at serine residue 203 in the nucleus, by combined treatment with dexamethasone and PD98059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 193-200 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-31 18459800-0 2008 Mapping peptide hormone-receptor interactions using a disulfide-trapping approach. Disulfides 54-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 16-32 18460448-1 2008 1,1-Bis(3"-indolyl)-1-(p-substituted phenyl)methanes (C-DIMs) activate the orphan receptors peroxisome proliferator-activated receptor gamma (PPARgamma) and Nur77 and induce receptor-dependent and -independent apoptotic pathways in colon and other cancer cells. 1,1-bis(3"-indolyl)-1-(p-substituted phenyl)methanes 0-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-162 18460448-1 2008 1,1-Bis(3"-indolyl)-1-(p-substituted phenyl)methanes (C-DIMs) activate the orphan receptors peroxisome proliferator-activated receptor gamma (PPARgamma) and Nur77 and induce receptor-dependent and -independent apoptotic pathways in colon and other cancer cells. c-dims 54-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 157-162 18202854-0 2008 Induction of apoptosis in PA-1 ovarian cancer cells by vitamin K2 is associated with an increase in the level of TR3/Nur77 and its accumulation in mitochondria and nuclei. Vitamin K 2 55-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-116 18202854-0 2008 Induction of apoptosis in PA-1 ovarian cancer cells by vitamin K2 is associated with an increase in the level of TR3/Nur77 and its accumulation in mitochondria and nuclei. Vitamin K 2 55-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 117-122 18202854-9 2008 Treatment of PA-1 cells with small interfering RNA (siRNA) directed against TR3, and with cycloheximide or SP600125 (an inhibitor of c-jun N-terminal kinase; JNK), separately, inhibited the VK(2)-induced synthesis of TR3 and apoptosis. Cycloheximide 90-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 217-220 18202854-9 2008 Treatment of PA-1 cells with small interfering RNA (siRNA) directed against TR3, and with cycloheximide or SP600125 (an inhibitor of c-jun N-terminal kinase; JNK), separately, inhibited the VK(2)-induced synthesis of TR3 and apoptosis. pyrazolanthrone 107-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 217-220 18466322-3 2008 Another class of transcription factors, namely, the nuclear receptor subgroup called Nurs (Nur77, Nurr1 and Nor-1), has recently been associated with behavioral and biochemical effects mediated by dopamine. Dopamine 197-205 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-96 18466322-8 2008 Interestingly, modulation of dopamine drug-induced locomotor activities by kinase inhibitors is in accordance with the effects on Nur77, but not Nor-1, expression. Dopamine 29-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 130-135 18075758-10 2008 CONCLUSIONS: These data support the findings of the main PROACT trial, which confirmed that anastrozole, as compared with tamoxifen, is an effective neoadjuvant endocrine treatment in objective response rates for postmenopausal women with large operable hormone-receptor positive breast cancer. Anastrozole 92-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 254-270 18163434-5 2008 The transcriptional regulation of NGFI-B/Nur77 by LH/human chorionic gonadotropin (hCG) or 8-bromoadenosine 3"-5"-cyclic monophosphate (8 Br-cAMP) was examined in mouse Leydig tumor cells MA-10. 8-Bromo Cyclic Adenosine Monophosphate 91-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-40 18048288-7 2008 Steroid hormone target sensitivity can be affected by variables such as metabolizing enzyme activity, hormone receptor expression as well as receptor cofactor expression. Steroids 0-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-118 18163434-5 2008 The transcriptional regulation of NGFI-B/Nur77 by LH/human chorionic gonadotropin (hCG) or 8-bromoadenosine 3"-5"-cyclic monophosphate (8 Br-cAMP) was examined in mouse Leydig tumor cells MA-10. 8-Bromo Cyclic Adenosine Monophosphate 91-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 18163434-5 2008 The transcriptional regulation of NGFI-B/Nur77 by LH/human chorionic gonadotropin (hCG) or 8-bromoadenosine 3"-5"-cyclic monophosphate (8 Br-cAMP) was examined in mouse Leydig tumor cells MA-10. 8-Bromo Cyclic Adenosine Monophosphate 138-145 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-40 18163434-5 2008 The transcriptional regulation of NGFI-B/Nur77 by LH/human chorionic gonadotropin (hCG) or 8-bromoadenosine 3"-5"-cyclic monophosphate (8 Br-cAMP) was examined in mouse Leydig tumor cells MA-10. 8-Bromo Cyclic Adenosine Monophosphate 138-145 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-46 17957723-0 2008 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane activates Nur77-independent proapoptotic responses in colon cancer cells. 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane 0-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-62 18454044-2 2008 For more than 2 decades, tamoxifen has been the standard endocrine agent for hormone receptor-positive tumors. Tamoxifen 25-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-93 18037293-0 2008 Vitamin D supplementation and response to aromatase inhibitors in postmenopausal women with hormone-receptor positive breast cancer. Vitamin D 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-108 18316794-0 2008 Double-blind, randomized placebo controlled trial of fulvestrant compared with exemestane after prior nonsteroidal aromatase inhibitor therapy in postmenopausal women with hormone receptor-positive, advanced breast cancer: results from EFECT. Fulvestrant 53-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 172-188 17653859-0 2008 Cost-effectiveness of letrozole versus tamoxifen as initial adjuvant therapy in postmenopausal women with hormone-receptor positive early breast cancer from a Canadian perspective. Letrozole 22-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-122 17957723-1 2008 1,1-Bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) is a methylene-substituted diindolylmethane (C-DIM) analog that activates the orphan receptor nerve growth factor-induced-Balpha (NGFI-Balpha, Nur77). 1,1-bis(3"-indolyl)-1-(p-methoxyphenyl)methane 0-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 17957723-1 2008 1,1-Bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) is a methylene-substituted diindolylmethane (C-DIM) analog that activates the orphan receptor nerve growth factor-induced-Balpha (NGFI-Balpha, Nur77). dim-c-pphoch 48-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 17957723-1 2008 1,1-Bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) is a methylene-substituted diindolylmethane (C-DIM) analog that activates the orphan receptor nerve growth factor-induced-Balpha (NGFI-Balpha, Nur77). methylene-substituted diindolylmethane 70-108 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 17957723-1 2008 1,1-Bis(3"-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) is a methylene-substituted diindolylmethane (C-DIM) analog that activates the orphan receptor nerve growth factor-induced-Balpha (NGFI-Balpha, Nur77). c-dim 110-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 17957723-7 2008 Thus, the effectiveness of DIM-C-pPhOCH(3) as a tumor growth inhibitor is through activation of Nur77-dependent and -independent pathways. dim-c-pphoch 27-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-101 18288313-0 2008 Arsenic as an endocrine disruptor: arsenic disrupts retinoic acid receptor-and thyroid hormone receptor-mediated gene regulation and thyroid hormone-mediated amphibian tail metamorphosis. Arsenic 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-103 18248459-2 2008 As a transcription factor, Nur77 participates in a variety of biological processes, including T cell development, inflammatory responses, steroid hormone synthesis, and hepatic glucose metabolism. Steroids 138-153 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-32 18622910-1 2008 Tamoxifen is the standard treatment in premenopausal hormone-receptor positive breast cancer patients with additional benefit in some of these women by adding ovarian ablation or suppression. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-69 18622910-9 2008 In selected postmenopausal patients with hormone-receptor positive disease the use of five years of tamoxifen can still be a viable option. Tamoxifen 100-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-57 18225870-1 2008 Time-resolved resonance Raman (TR3) studies of the photochemistry of phenyl azide, 3-hyroxyphenyl azide, 3-methoxyphenyl azide and 3-nitrophenyl azide in acetonitrile:water solutions is reported. phenylazide 69-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-34 18225870-1 2008 Time-resolved resonance Raman (TR3) studies of the photochemistry of phenyl azide, 3-hyroxyphenyl azide, 3-methoxyphenyl azide and 3-nitrophenyl azide in acetonitrile:water solutions is reported. 3-hyroxyphenyl azide 83-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-34 18225870-1 2008 Time-resolved resonance Raman (TR3) studies of the photochemistry of phenyl azide, 3-hyroxyphenyl azide, 3-methoxyphenyl azide and 3-nitrophenyl azide in acetonitrile:water solutions is reported. 3-methoxyphenyl azide 105-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-34 18225870-1 2008 Time-resolved resonance Raman (TR3) studies of the photochemistry of phenyl azide, 3-hyroxyphenyl azide, 3-methoxyphenyl azide and 3-nitrophenyl azide in acetonitrile:water solutions is reported. 3-nitrophenyl azide 131-150 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-34 18225870-2 2008 After photolysis of these four aryl azides in room temperature solutions, only one species was observed in the TR3 spectra for each azide, respectively at the probe wavelengths employed in the TR3 experiments. aryl azides 31-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-114 18225870-2 2008 After photolysis of these four aryl azides in room temperature solutions, only one species was observed in the TR3 spectra for each azide, respectively at the probe wavelengths employed in the TR3 experiments. aryl azides 31-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 193-196 18225870-2 2008 After photolysis of these four aryl azides in room temperature solutions, only one species was observed in the TR3 spectra for each azide, respectively at the probe wavelengths employed in the TR3 experiments. Azides 36-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-114 18225870-2 2008 After photolysis of these four aryl azides in room temperature solutions, only one species was observed in the TR3 spectra for each azide, respectively at the probe wavelengths employed in the TR3 experiments. Azides 36-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 193-196 18288313-0 2008 Arsenic as an endocrine disruptor: arsenic disrupts retinoic acid receptor-and thyroid hormone receptor-mediated gene regulation and thyroid hormone-mediated amphibian tail metamorphosis. Arsenic 35-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-103 17939708-1 2007 A nanosecond time-resolved resonance Raman (ns-TR3) spectroscopic study of the reactions of the 2-fluorenylnitrenium ion with several C8-substituted guanosine derivatives is reported. 2-fluorenylnitrenium 96-116 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-50 17693420-6 2008 Compared with tamoxifen, anastrozole and letrozole significantly improved disease-free survival as early adjuvant treatment for hormone-receptor-positive disease. Anastrozole 25-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 128-144 17693420-6 2008 Compared with tamoxifen, anastrozole and letrozole significantly improved disease-free survival as early adjuvant treatment for hormone-receptor-positive disease. Letrozole 41-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 128-144 18282367-1 2007 Third-generation aromatase inhibitors (AIs; anastrozole, letrozole, exemestane) have replaced tamoxifen as the adjuvant treatment of choice for postmenopausal women with hormone receptor-positive early-stage breast cancer. Letrozole 57-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 170-186 18282367-1 2007 Third-generation aromatase inhibitors (AIs; anastrozole, letrozole, exemestane) have replaced tamoxifen as the adjuvant treatment of choice for postmenopausal women with hormone receptor-positive early-stage breast cancer. exemestane 68-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 170-186 17892469-1 2007 The third-generation aromatase inhibitors (AIs) anastrozole, exemestane and letrozole have largely replaced tamoxifen as the preferred treatment for hormone receptor - positive breast cancer in postmenopausal women. Letrozole 76-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-165 17761950-8 2007 9-cis retinoic acid, a ligand for RXRalpha, enhanced the association of RXRalpha with TR3, rather than acetylation of RXRalpha by p300. Alitretinoin 0-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-89 17761950-10 2007 Upon the treatment of 9-cis retinoic acid, RXRalpha was translocated with TR3 from the nucleus to the mitochondria, and apoptosis was induced. Alitretinoin 22-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-77 18547136-1 2008 Anastrozole (Arimidex) is an aromatase inhibitor approved in the EU, the US and in other countries worldwide for use as an adjuvant treatment in postmenopausal women with early-stage, hormone receptor-positive breast cancer. Anastrozole 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 184-200 18547136-1 2008 Anastrozole (Arimidex) is an aromatase inhibitor approved in the EU, the US and in other countries worldwide for use as an adjuvant treatment in postmenopausal women with early-stage, hormone receptor-positive breast cancer. Anastrozole 13-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 184-200 18547136-4 2008 In patients with hormone receptor-positive tumours, 5 years of anastrozole treatment was more efficacious in reducing breast cancer recurrence than 5 years of tamoxifen, both in a head-to-head comparison and in switching trials when given after 2-3 years of tamoxifen treatment. Anastrozole 63-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-33 18547136-13 2008 However, the evidence to date establishes anastrozole as a valuable adjuvant and extended adjuvant treatment for postmenopausal women with hormone receptor-positive, early-stage breast cancer. Anastrozole 42-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-155 18073527-0 2007 Staurosporine sensitizes T lymphoma cells to glucocorticoid-induced apoptosis: role of Nur77 and Bcl-2. Staurosporine 0-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-92 17923408-7 2007 Hormone receptor (HR) status, one of the critical determinants of BC biology, had been suggested to be a factor modulating response to adjuvant chemotherapy in general and taxanes in particular. Taxoids 172-179 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 17923408-7 2007 Hormone receptor (HR) status, one of the critical determinants of BC biology, had been suggested to be a factor modulating response to adjuvant chemotherapy in general and taxanes in particular. Taxoids 172-179 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-20 17923408-9 2007 Indirect (retrospective, unplanned) analysis suggest that the magnitude of benefit from taxanes is somewhat more in the HR negative subset, but the benefit also exists, and is clinically relevant, in patients with HR positive cancers. Taxoids 88-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-122 17939708-1 2007 A nanosecond time-resolved resonance Raman (ns-TR3) spectroscopic study of the reactions of the 2-fluorenylnitrenium ion with several C8-substituted guanosine derivatives is reported. Guanosine 149-158 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-50 17939708-2 2007 The TR3 spectra show that the 2-fluorenylnitrenium ion reacts with the C8-substituted guanosine derivatives (C8-methylguanosine and C8-bromoguanosine) to produce C8 intermediates with the methyl and bromine moieties still attached to the intermediate species at the C8 position. 2-fluorenylnitrenium 30-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17939708-2 2007 The TR3 spectra show that the 2-fluorenylnitrenium ion reacts with the C8-substituted guanosine derivatives (C8-methylguanosine and C8-bromoguanosine) to produce C8 intermediates with the methyl and bromine moieties still attached to the intermediate species at the C8 position. Guanosine 86-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17939708-2 2007 The TR3 spectra show that the 2-fluorenylnitrenium ion reacts with the C8-substituted guanosine derivatives (C8-methylguanosine and C8-bromoguanosine) to produce C8 intermediates with the methyl and bromine moieties still attached to the intermediate species at the C8 position. c8-methylguanosine 109-127 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17939708-2 2007 The TR3 spectra show that the 2-fluorenylnitrenium ion reacts with the C8-substituted guanosine derivatives (C8-methylguanosine and C8-bromoguanosine) to produce C8 intermediates with the methyl and bromine moieties still attached to the intermediate species at the C8 position. c8-bromoguanosine 132-149 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17939708-2 2007 The TR3 spectra show that the 2-fluorenylnitrenium ion reacts with the C8-substituted guanosine derivatives (C8-methylguanosine and C8-bromoguanosine) to produce C8 intermediates with the methyl and bromine moieties still attached to the intermediate species at the C8 position. Bromine 199-206 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17701362-3 2007 Here it is shown that in thymic lymphoma cells resistant to calcium-mediated apoptosis, cytochrome c release is abolished despite of Nur77 mitochondrial targeting. Calcium 60-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-138 17785466-2 2007 We found that both NR4A3 and NR4A1 were induced by insulin and by thiazolidinedione drugs (pioglitazone and troglitazone) in 3T3-L1 adipocytes. 2,4-thiazolidinedione 66-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-34 17785466-2 2007 We found that both NR4A3 and NR4A1 were induced by insulin and by thiazolidinedione drugs (pioglitazone and troglitazone) in 3T3-L1 adipocytes. Pioglitazone 91-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-34 17785466-2 2007 We found that both NR4A3 and NR4A1 were induced by insulin and by thiazolidinedione drugs (pioglitazone and troglitazone) in 3T3-L1 adipocytes. Troglitazone 108-120 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-34 17675581-3 2007 To explore the functional importance of MR in mammalian skin, we have generated a conditional doxycycline-inducible model of MR overexpression, resulting in double-transgenic (DT) mice [keratin 5-tTa/tetO-human MR (hMR)], targeting the human MR specifically to keratinocytes of the epidermis and hair follicle (HF). Doxycycline 94-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-127 17715970-1 2007 A nanosecond time-resolved resonance Raman (ns-TR3) spectroscopic study of the triplet state benzophenone reaction with the 2-propanol hydrogen-donor solvent and subsequent reactions is presented. benzophenone 93-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-50 17715970-1 2007 A nanosecond time-resolved resonance Raman (ns-TR3) spectroscopic study of the triplet state benzophenone reaction with the 2-propanol hydrogen-donor solvent and subsequent reactions is presented. 2-Propanol 124-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-50 17715970-1 2007 A nanosecond time-resolved resonance Raman (ns-TR3) spectroscopic study of the triplet state benzophenone reaction with the 2-propanol hydrogen-donor solvent and subsequent reactions is presented. Hydrogen 135-143 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-50 17715970-2 2007 The TR3 spectra show that the benzophenone triplet state (npi*) hydrogen-abstraction reaction with 2-propanol is very fast (about 10 to 20 ns) and forms a diphenylketyl radical and an associated 2-propanol radical partner. benzophenone 30-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17715970-2 2007 The TR3 spectra show that the benzophenone triplet state (npi*) hydrogen-abstraction reaction with 2-propanol is very fast (about 10 to 20 ns) and forms a diphenylketyl radical and an associated 2-propanol radical partner. Hydrogen 64-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17715970-2 2007 The TR3 spectra show that the benzophenone triplet state (npi*) hydrogen-abstraction reaction with 2-propanol is very fast (about 10 to 20 ns) and forms a diphenylketyl radical and an associated 2-propanol radical partner. 2-Propanol 99-109 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17715970-2 2007 The TR3 spectra show that the benzophenone triplet state (npi*) hydrogen-abstraction reaction with 2-propanol is very fast (about 10 to 20 ns) and forms a diphenylketyl radical and an associated 2-propanol radical partner. diphenylketyl radical 155-176 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17715970-2 2007 The TR3 spectra show that the benzophenone triplet state (npi*) hydrogen-abstraction reaction with 2-propanol is very fast (about 10 to 20 ns) and forms a diphenylketyl radical and an associated 2-propanol radical partner. 2-propanol radical 195-213 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 17715970-3 2007 The temporal evolution of the TR3 spectra also indicates that recombination of these two radical species occurs with a time constant of about 1170 ns to produce a LAT (light absorbing transient) intermediate that is identified as the 2-[4-(hydroxylphenylmethylene)cyclohexa-2,5-dienyl]propan-2-ol (p-LAT) species. Lactose 163-166 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-33 17715970-3 2007 The temporal evolution of the TR3 spectra also indicates that recombination of these two radical species occurs with a time constant of about 1170 ns to produce a LAT (light absorbing transient) intermediate that is identified as the 2-[4-(hydroxylphenylmethylene)cyclohexa-2,5-dienyl]propan-2-ol (p-LAT) species. 2-[4-(hydroxylphenylmethylene)cyclohexa-2,5-dienyl]propan-2-ol 234-296 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-33 17715970-3 2007 The temporal evolution of the TR3 spectra also indicates that recombination of these two radical species occurs with a time constant of about 1170 ns to produce a LAT (light absorbing transient) intermediate that is identified as the 2-[4-(hydroxylphenylmethylene)cyclohexa-2,5-dienyl]propan-2-ol (p-LAT) species. p-lat 298-303 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-33 17890213-7 2007 Tamoxifen has been the gold standard endocrine therapy for hormone-receptor-positive early breast cancer for many years, and the long-term side effects of this agent are well documented. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-75 17675581-3 2007 To explore the functional importance of MR in mammalian skin, we have generated a conditional doxycycline-inducible model of MR overexpression, resulting in double-transgenic (DT) mice [keratin 5-tTa/tetO-human MR (hMR)], targeting the human MR specifically to keratinocytes of the epidermis and hair follicle (HF). Doxycycline 94-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-127 17675581-3 2007 To explore the functional importance of MR in mammalian skin, we have generated a conditional doxycycline-inducible model of MR overexpression, resulting in double-transgenic (DT) mice [keratin 5-tTa/tetO-human MR (hMR)], targeting the human MR specifically to keratinocytes of the epidermis and hair follicle (HF). Doxycycline 94-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-127 17574328-6 2007 MEHP-induced Nur77 transcription was inhibited by bisindolylmaleimide I (protein kinase C inhibitor) and wortmannin (phosphoinositide 3-kinase inhibitor). mono-(2-ethylhexyl)phthalate 0-4 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 17588685-0 2007 Ionomycin-induced apoptosis of thymocytes is independent of Nur77 NBRE or NurRE binding, but is accompanied by Nur77 mitochondrial targeting. Ionomycin 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-65 17588685-0 2007 Ionomycin-induced apoptosis of thymocytes is independent of Nur77 NBRE or NurRE binding, but is accompanied by Nur77 mitochondrial targeting. Ionomycin 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-116 17588685-2 2007 Ionomycin treatment induces endogenous Nur77 expression as well as apoptosis and cytochrome c release in thymocytes. Ionomycin 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 17588685-3 2007 Here it is shown for the first time that in normal thymocytes undergoing apoptosis, ionomycin induces translocation of endogenous Nur77 not only to the nucleus, but also to mitochondria. Ionomycin 84-93 nuclear receptor subfamily 4 group A member 1 Homo sapiens 130-135 17588685-4 2007 Immunosuppressant FK506 inhibits Nur77 NBRE and NurRE binding activity but has no effect on thymocytes apoptosis, the subcellular localization of Nur77, or cytochrome c release. Tacrolimus 18-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-38 17574328-6 2007 MEHP-induced Nur77 transcription was inhibited by bisindolylmaleimide I (protein kinase C inhibitor) and wortmannin (phosphoinositide 3-kinase inhibitor). bisindolylmaleimide I 50-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 17574328-6 2007 MEHP-induced Nur77 transcription was inhibited by bisindolylmaleimide I (protein kinase C inhibitor) and wortmannin (phosphoinositide 3-kinase inhibitor). Wortmannin 105-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 17574328-7 2007 Finally, ectopic expression of Nur77 markedly suppressed forskolin-induced transcriptional activation of promoters I.3 and II of the CYP19 gene. Colforsin 57-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-36 17690028-6 2007 RESULTS: We propose some new strategies to achieve transplant tolerance in rodent animals via manipulating Treg function, including using histone deacetylase (HDAC) inhibitor to regulate Foxp3 transcription and enhance Treg suppression, induction of Treg-sparing apoptosis via Nur77, and identification of the co-inhibitory molecule herpes virus entry mediator (HVEM) as an effector molecule for Treg function. treg 107-111 nuclear receptor subfamily 4 group A member 1 Homo sapiens 277-282 17543302-3 2007 The present study was designed to determine the intracellular localization of TR3 following CD437-induced nucleocytoplasmic translocation and the mechanisms involved in TR3-induced apoptosis. CD 437 92-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-81 17601725-2 2007 Using a methylation microarray, we analysed 117 candidate genes in hormone receptor-positive tumours from 109 breast cancer patients treated by adjuvant tamoxifen. Tamoxifen 153-162 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-83 17600153-3 2007 To unveil the structural organization of NGFI-B in solution, we determined the quaternary structure of the NGFI-B LBD by a combination of ab initio procedures from small-angle X-ray scattering (SAXS) data and hydrogen-deuterium exchange followed by mass spectrometry. Deuterium 218-227 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-113 17601725-10 2007 Based on PITX2 methylation, about half of hormone receptor-positive, node-negative breast cancer patients receiving adjuvant tamoxifen monotherapy can be considered low-risk regarding development of distant recurrences and may thus be spared adjuvant chemotherapy. Tamoxifen 125-134 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-58 17146432-0 2007 6-Mercaptopurine, an activator of Nur77, enhances transcriptional activity of HIF-1alpha resulting in new vessel formation. Mercaptopurine 0-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-39 17515570-0 2007 Poor outcome of hormone receptor-positive breast cancer at very young age is due to tamoxifen resistance: nationwide survival data in Korea--a report from the Korean Breast Cancer Society. Tamoxifen 84-93 nuclear receptor subfamily 4 group A member 1 Homo sapiens 16-32 17450590-0 2007 Prognostic factors of early distant recurrence in hormone receptor-positive, postmenopausal breast cancer patients receiving adjuvant tamoxifen therapy: results of a retrospective analysis. Tamoxifen 134-143 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-66 17450590-3 2007 The authors conducted a retrospective analysis to identify risk factors of early recurrences in hormone receptor (HR)-positive, postmenopausal women within the first 3 years of adjuvant tamoxifen. Tamoxifen 186-195 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-112 17450590-3 2007 The authors conducted a retrospective analysis to identify risk factors of early recurrences in hormone receptor (HR)-positive, postmenopausal women within the first 3 years of adjuvant tamoxifen. Tamoxifen 186-195 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-116 17439837-9 2007 In LNNBCs with positive HR status, HER-2 overexpression and/or amplification confer an aggressive tumor phenotype, and this might be related to tamoxifen unresponsiveness. Tamoxifen 144-153 nuclear receptor subfamily 4 group A member 1 Homo sapiens 24-26 17023523-4 2007 Here we showed that JNK activator anisomycin induced TR3 phosphorylation through JNK1 rather than p38 and ERK signals, which is mediated by its upstream factors MAPK kinase 4 and MAPK kinase 7. Anisomycin 34-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-56 17690503-0 2007 Relation of serum levels of estrogen and dehydroepiandrosterone sulfate to hormone receptor status among postmenopausal women with breast cancer. Dehydroepiandrosterone Sulfate 41-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 18062723-5 2007 In a noncomparative phase II study of trastuzumab plus letrozole in postmenopausal women with HER2 and HR co-positive metastatic breast cancer, the majority of adverse events were mild or moderate in severity. Letrozole 55-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 103-105 17492927-5 2007 Letrozole is the only aromatase inhibitor to demonstrate a significant 27% reduction in the risk of distant metastases (p = 0.001) in the clinically relevant, hormone receptor-positive population in the initial adjuvant setting. Letrozole 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-175 17234778-4 2007 The induction of apoptosis and TRAIL by DIM-C-pPhOCH3 was significantly inhibited by a small inhibitory RNA for Nur77 (iNur77); however, it was evident from RNA interference studies that DIM-C-pPhOCH3 also induced Nur77-independent apoptosis. DIM-C-pPhOCH3 40-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-117 17234778-4 2007 The induction of apoptosis and TRAIL by DIM-C-pPhOCH3 was significantly inhibited by a small inhibitory RNA for Nur77 (iNur77); however, it was evident from RNA interference studies that DIM-C-pPhOCH3 also induced Nur77-independent apoptosis. DIM-C-pPhOCH3 40-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-125 17234778-4 2007 The induction of apoptosis and TRAIL by DIM-C-pPhOCH3 was significantly inhibited by a small inhibitory RNA for Nur77 (iNur77); however, it was evident from RNA interference studies that DIM-C-pPhOCH3 also induced Nur77-independent apoptosis. DIM-C-pPhOCH3 187-200 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-125 17234778-5 2007 Analysis of DIM-C-pPhOCH3-induced gene expression using microarrays identified several proapoptotic genes, and analysis by reverse transcription-PCR in the presence or absence of iNur77 showed that induction of programmed cell death gene 1 was Nur77 dependent, whereas induction of cystathionase and activating transcription factor 3 was Nur77 independent. DIM-C-pPhOCH3 12-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 244-249 17023523-5 2007 We also identified the exact phosphorylation site of JNK to be serine 95 at the N terminus of TR3, around which a classical JNK phosphorylation motif exists. Serine 63-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-97 17566296-4 2007 At present, the identity of the receptor is unknown; the hormone-receptor interactions are facilitated by albumin and disulphide bonds. disulphide 118-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-73 17220670-6 2007 Therefore, HR and HER 2 were associated with the sensitivity to a chemotherapeutic agent, taxane. taxane 90-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-13 17150035-6 2007 Agents, such as 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic acid (AHPN/CD437), which induce Nur77 migration from the nucleus to mitochondria, effectively induce apoptosis of cancer cells. CD 437 16-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-114 17220670-2 2007 Among the patients treated with taxane alone,the response rates were 37.5% (n=67) in the HR (+) patients and 14.6% (n=41) in the HR (-) patients (p=0.0131). taxane 32-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-91 17220670-3 2007 In particular, taxane resistance was suggested in the HR (-)/HER 2 (-) patients (response rate: 4.2%, n=24). taxane 15-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-56 17220670-4 2007 Concerning combination therapy with trastuzumab and taxane, the response rate were 52.8% in the HR (+)/HER 2 (+) patients and 60.4% in the HR (-)/HER 2 (+) patients. taxane 52-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-98 17220670-4 2007 Concerning combination therapy with trastuzumab and taxane, the response rate were 52.8% in the HR (+)/HER 2 (+) patients and 60.4% in the HR (-)/HER 2 (+) patients. taxane 52-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-141 17220670-5 2007 In 27 of these patients, single therapy with taxane was switched to combination therapy with taxane and trastuzumab after they became resistant to taxane, and 8.3% of the HR (+)/HER 2 (+) patients and 53.3% of the HR (-)/HER 2 (+) patients responded to this combination therapy (p=0.0192), suggesting the synergistic effects of the two agents in HR (-)/HER 2 (+) patients. taxane 45-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-173 16904076-2 2006 Details of interaction revealed that C-terminal ligand binding domain (LBD) of Nur77 specifically interacted with highly conserved glycine-rich loop of PKC required for catalytic activity. Glycine 131-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 79-84 16574409-2 2006 Extent of primary biodegradation of a nonylphenol ethoxylates (NP-10) was excess of 92% after 1.5 days, and reached 99% after 2 days, which was similar to the results obtained using modified CTAS (thiocyanate active substances) method. ethoxylates 50-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 16574409-2 2006 Extent of primary biodegradation of a nonylphenol ethoxylates (NP-10) was excess of 92% after 1.5 days, and reached 99% after 2 days, which was similar to the results obtained using modified CTAS (thiocyanate active substances) method. thiocyanate 197-208 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 16574409-3 2006 Degradation of benzene ring of NP-10 was studied using UV-absorbance at 277 nm in chloroform. Benzene 15-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-36 16574409-3 2006 Degradation of benzene ring of NP-10 was studied using UV-absorbance at 277 nm in chloroform. Chloroform 82-92 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-36 17134767-0 2007 Nur77 and retinoid X receptors: crucial factors in dopamine-related neuroadaptation. Dopamine 51-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 16959170-26 2006 We accepted that hormone receptor status (ER) for hormonal therapy such as tamoxifen and prediction of response to trastuzumab by HER2 did not require systematic review, as the mechanism of action of these drugs requires intact receptors. Tamoxifen 75-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-33 16940812-6 2006 We treated three premenopausal patients with hormone receptor-positive metastatic breast cancer with combined oophorectomy or ovarian irradiation and anastrozole. Anastrozole 150-161 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-61 16827799-0 2006 Alternative tyrosine phosphorylation of signaling kinases according to hormone receptor status in breast cancer overexpressing the insulin-like growth factor receptor type 1. Tyrosine 12-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-87 16760268-1 2006 BACKGROUND: Hormone receptor (HR)-positive breast cancer cells grow through estrogen receptor (ER)-signaling pathways that mediate both genomic and nongenomic actions, which cross-talk with growth factors associated with resistance to tamoxifen. Tamoxifen 235-244 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-28 16760268-1 2006 BACKGROUND: Hormone receptor (HR)-positive breast cancer cells grow through estrogen receptor (ER)-signaling pathways that mediate both genomic and nongenomic actions, which cross-talk with growth factors associated with resistance to tamoxifen. Tamoxifen 235-244 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-32 16899609-1 2006 PURPOSE: Tamoxifen has long been the drug of choice in adjuvant endocrine therapy of steroid hormone receptor-positive breast cancer, and it still remains important due to its well-documented beneficial effect. Tamoxifen 9-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-109 16413707-0 2006 Does tamoxifen therapy affect the hormone receptor expression and cell proliferation indices of endometrial polyps? Tamoxifen 5-14 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-50 16413707-8 2006 CONCLUSIONS: Tamoxifen has a significant affect on hormone receptor expression and markers of apoptosis in endometrial polyps. Tamoxifen 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-67 16434970-2 2006 Nur77 translocation is induced by certain apoptotic stimuli, including the synthetic retinoid-related 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalenecarboxylic acid (AHPN)/CD437 class. Retinoids 85-93 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 16723716-7 2006 Finally, stretch-mediated proliferation was inhibited by 6-mercaptopurine, an agonist of TR3. Mercaptopurine 57-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-92 16434970-6 2006 In addition, several JNK upstream activators, including the phorbol ester TPA, anisomycin and MAPK kinase kinase-1 (MEKK1), phosphorylated Nur77 and induced its nuclear export. Phorbol Esters 60-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 16434970-2 2006 Nur77 translocation is induced by certain apoptotic stimuli, including the synthetic retinoid-related 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalenecarboxylic acid (AHPN)/CD437 class. CD 437 102-166 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 16434970-6 2006 In addition, several JNK upstream activators, including the phorbol ester TPA, anisomycin and MAPK kinase kinase-1 (MEKK1), phosphorylated Nur77 and induced its nuclear export. Tetradecanoylphorbol Acetate 74-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 16434970-6 2006 In addition, several JNK upstream activators, including the phorbol ester TPA, anisomycin and MAPK kinase kinase-1 (MEKK1), phosphorylated Nur77 and induced its nuclear export. Anisomycin 79-89 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 16434970-2 2006 Nur77 translocation is induced by certain apoptotic stimuli, including the synthetic retinoid-related 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalenecarboxylic acid (AHPN)/CD437 class. CD 437 174-179 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 16434970-3 2006 In this study, we investigated the molecular mechanism by which AHPN/CD437 analog (E)-4-[3-(1-adamantyl)-4-hydroxyphenyl]-3-chlorocinnamic acid (3-Cl-AHPC) induces Nur77 nuclear export. CD 437 64-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-169 16434970-3 2006 In this study, we investigated the molecular mechanism by which AHPN/CD437 analog (E)-4-[3-(1-adamantyl)-4-hydroxyphenyl]-3-chlorocinnamic acid (3-Cl-AHPC) induces Nur77 nuclear export. CD 437 69-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-169 16434970-3 2006 In this study, we investigated the molecular mechanism by which AHPN/CD437 analog (E)-4-[3-(1-adamantyl)-4-hydroxyphenyl]-3-chlorocinnamic acid (3-Cl-AHPC) induces Nur77 nuclear export. 4-(3-(1-adamantyl)-4-hydroxyphenyl)-3-chlorocinnamic acid 82-143 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-169 16434970-3 2006 In this study, we investigated the molecular mechanism by which AHPN/CD437 analog (E)-4-[3-(1-adamantyl)-4-hydroxyphenyl]-3-chlorocinnamic acid (3-Cl-AHPC) induces Nur77 nuclear export. 4-(3-(1-adamantyl)-4-hydroxyphenyl)-3-chlorocinnamic acid 145-154 nuclear receptor subfamily 4 group A member 1 Homo sapiens 164-169 16434970-4 2006 Our results demonstrate that 3-Cl-AHPC effectively activated Jun N-terminal kinase (JNK), which phosphorylates Nur77. 3-cl 29-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 111-116 16434970-5 2006 Inhibition of JNK activation by a JNK inhibitor suppressed 3-Cl-AHPC-induced Nur77 nuclear export and apoptosis. 4-(3-(1-adamantyl)-4-hydroxyphenyl)-3-chlorocinnamic acid 59-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-82 16631355-0 2006 Reduction of dopamine-related transcription factors Nurr1 and NGFI-B in the prefrontal cortex in schizophrenia and bipolar disorders. Dopamine 13-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-68 16585961-9 2006 In concert, these data promote a distinctive mechanism for normal human development whereby cortisol production, determined by transient NGFI-B and HSD3B2 expression, provides feedback at the anterior pituitary to modulate androgen biosynthesis and safeguard normal female sexual differentiation. Hydrocortisone 92-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-143 16446340-1 2006 PURPOSE: Adjuvant chemotherapy followed by tamoxifen is a standard treatment option for women with intermediate or high-risk hormone receptor-positive breast cancer. Tamoxifen 43-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 16493264-6 2006 In addition, some epidemiologic studies have reported that hormone-receptor-positive breast tumors are more responsive to aspirin, which is consistent with these preclinical findings. Aspirin 122-129 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-75 16293862-12 2005 TAM is effective in HR-positive disease, but not in HR-negative disease. Tamoxifen 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-22 16392918-5 2005 Despite this, the attraction basin around each GM is relatively large, since after all their atomic coordinates are randomly displaced by values as high as 2.0 bohrs, the perturbed structures, upon reoptimization, relax back to the GM in more than 50% of the cases (except for n=10 and 11). gm 47-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 277-288 16198568-3 2005 Tamoxifen significantly decreases the risk of recurrence and improves survival in all women with hormone receptor-positive invasive breast cancer, including women 70 years and older. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-113 16204640-10 2005 Three of those (an orphan nuclear receptor NUR77, a guanosine 5"-diphosphate/guanosine 5"-triphosphate exchange factor RABEX5, and a PRK1-associated protein AWP1) were particularly potent inhibitors of NF-kappaB activation. Guanosine Triphosphate 77-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-48 16288995-2 2005 Although NGFI-B also forms a heterodimer with the retinoid X receptor (RXR), a receptor for 9-cis retinoic acid (9CRA), endogenous targets of the heterodimer have not been identified. Alitretinoin 92-111 nuclear receptor subfamily 4 group A member 1 Homo sapiens 9-15 16288995-3 2005 We investigated the role of RXR ligand binding in NGFI-B/RXR activation and found that dibenzodiazepine-derived ligands, such as the weak RXR agonist HX600, selectively activate NGFI-B/RXR heterodimers. 6-benzyl-5H-dibenzodiazepine 87-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-56 16288995-3 2005 We investigated the role of RXR ligand binding in NGFI-B/RXR activation and found that dibenzodiazepine-derived ligands, such as the weak RXR agonist HX600, selectively activate NGFI-B/RXR heterodimers. 6-benzyl-5H-dibenzodiazepine 87-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 178-184 16293862-6 2005 CAF had slightly better OS than CMF (85% v 82%, HR = 1.19 for CMF v CAF; 95% CI, 0.99 to 1.43); values were statistically significant in the planned one-sided test (P = .03). cafestol palmitate 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-50 15896973-6 2005 In this specific territory, the number of Nur77-positive cells was decreased, in response to L-DOPA, when compared to the medial part of the lesioned striatum. Levodopa 93-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-47 16293862-9 2005 For HR-positive patients, TAM was beneficial (DFS, HR = 1.32 for no TAM v TAM; 95% CI, 1.09 to 1.61; P = .003; OS, HR = 1.26; 95% CI, 0.99 to 1.61; P = .03), but not for HR-negative patients (DFS, HR = 0.81 for no TAM v TAM; 95% CI, 0.64 to 1.03; OS, HR = 0.79; 95% CI, 0.60 to 1.05). Tamoxifen 26-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-6 16293862-9 2005 For HR-positive patients, TAM was beneficial (DFS, HR = 1.32 for no TAM v TAM; 95% CI, 1.09 to 1.61; P = .003; OS, HR = 1.26; 95% CI, 0.99 to 1.61; P = .03), but not for HR-negative patients (DFS, HR = 0.81 for no TAM v TAM; 95% CI, 0.64 to 1.03; OS, HR = 0.79; 95% CI, 0.60 to 1.05). Tamoxifen 26-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-53 16293862-9 2005 For HR-positive patients, TAM was beneficial (DFS, HR = 1.32 for no TAM v TAM; 95% CI, 1.09 to 1.61; P = .003; OS, HR = 1.26; 95% CI, 0.99 to 1.61; P = .03), but not for HR-negative patients (DFS, HR = 0.81 for no TAM v TAM; 95% CI, 0.64 to 1.03; OS, HR = 0.79; 95% CI, 0.60 to 1.05). Tamoxifen 26-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-53 16293862-9 2005 For HR-positive patients, TAM was beneficial (DFS, HR = 1.32 for no TAM v TAM; 95% CI, 1.09 to 1.61; P = .003; OS, HR = 1.26; 95% CI, 0.99 to 1.61; P = .03), but not for HR-negative patients (DFS, HR = 0.81 for no TAM v TAM; 95% CI, 0.64 to 1.03; OS, HR = 0.79; 95% CI, 0.60 to 1.05). Tamoxifen 26-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-53 16293862-9 2005 For HR-positive patients, TAM was beneficial (DFS, HR = 1.32 for no TAM v TAM; 95% CI, 1.09 to 1.61; P = .003; OS, HR = 1.26; 95% CI, 0.99 to 1.61; P = .03), but not for HR-negative patients (DFS, HR = 0.81 for no TAM v TAM; 95% CI, 0.64 to 1.03; OS, HR = 0.79; 95% CI, 0.60 to 1.05). Tamoxifen 26-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-53 16293862-9 2005 For HR-positive patients, TAM was beneficial (DFS, HR = 1.32 for no TAM v TAM; 95% CI, 1.09 to 1.61; P = .003; OS, HR = 1.26; 95% CI, 0.99 to 1.61; P = .03), but not for HR-negative patients (DFS, HR = 0.81 for no TAM v TAM; 95% CI, 0.64 to 1.03; OS, HR = 0.79; 95% CI, 0.60 to 1.05). Tamoxifen 26-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-53 16197980-1 2005 The biotransformation and mineralization of a mixture of two polycyclic aromatic hydrocarbons (PAHs), anthracene and pyrene, which are known contaminants of soil and groundwater, by an enrichment culture in the presence or absence of 100 mg l(-1) Tergitol NP-10, a non-ionic surfactant, and at temperatures of 10 degrees C and 25 degrees C were investigated. Polycyclic Aromatic Hydrocarbons 95-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 256-261 16197980-1 2005 The biotransformation and mineralization of a mixture of two polycyclic aromatic hydrocarbons (PAHs), anthracene and pyrene, which are known contaminants of soil and groundwater, by an enrichment culture in the presence or absence of 100 mg l(-1) Tergitol NP-10, a non-ionic surfactant, and at temperatures of 10 degrees C and 25 degrees C were investigated. pyrene 117-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 256-261 15896973-7 2005 L-DOPA treatment increased dopamine D3 receptor and glutamate transporter 1 (GLT1) mRNA expression in the lesioned striatum and that, specifically in an area overlapping one of Nur77 decrease and of NT/DYN induction. Levodopa 0-6 nuclear receptor subfamily 4 group A member 1 Homo sapiens 177-182 16009706-1 2005 A series of 30 N10-substituted phenoxazines were synthesized and screened as potential inhibitors of Akt. phenoxazine 31-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-18 16264271-2 2005 It has been shown that the Nur77 promoter is activated by at least two signaling pathways, one mediated by calcium and the other by protein kinase C (PKC). Calcium 107-114 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-32 16264271-3 2005 MEF2D has been known to regulate Nur77 expression in a calcium- dependent manner. Calcium 55-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-38 16140267-9 2005 This finding represents a novel crosstalk between ERK2 and RXR signaling pathways, and explains how two independent inhibitors of apoptosis (EGF and 9-cis-retinoic acid) may cooperate to regulate nuclear targeting of apoptosis inducer NGFI-B. Alitretinoin 149-168 nuclear receptor subfamily 4 group A member 1 Homo sapiens 235-241 16205597-6 2005 It is well established that tamoxifen (T), a selective estrogen receptor modulator (SERM), improves overall survival (OS) in women with hormone receptor (HR) positive breast cancer. Tamoxifen 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 136-152 16205597-6 2005 It is well established that tamoxifen (T), a selective estrogen receptor modulator (SERM), improves overall survival (OS) in women with hormone receptor (HR) positive breast cancer. Tamoxifen 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-156 16051191-0 2005 Nur77 nuclear import and its NBRE-binding activity in thymic lymphoma cells are regulated by different mechanisms sensitive to FK506 or HA1004. Tacrolimus 127-132 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 16009706-3 2005 Substitutions at the 2-position (Cl or CF3) did not alter inhibitory activity, whereas N10-substitutions with derivatives having acetyl (20B) or morpholino (12B) side chain lost activity compared with propyl or butyl substituents (7B and 14B). Cysteine 129-135 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-90 16051191-0 2005 Nur77 nuclear import and its NBRE-binding activity in thymic lymphoma cells are regulated by different mechanisms sensitive to FK506 or HA1004. N-(2-guanidinoethyl)-5-isoquinolinesulfonamide 136-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 16051191-2 2005 In apoptosis-resistant cells, ionomycin-induced Nur77 strongly binds DNA during the first 2 h of response, in contrast to lymphoma cells treated with ionomycin together with FK506 or HA1004, which undergo massive apoptosis. Ionomycin 30-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 16051191-3 2005 We show that Nur77 could discriminate between calcium signals sensitive to FK506 and those sensitive to HA1004, as the inhibitors differentially regulate the kinetics of Nur77 nuclear import, and FK506, unlike HA1004, inhibits Nur77 DNA-binding activity. Calcium 46-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 16051191-3 2005 We show that Nur77 could discriminate between calcium signals sensitive to FK506 and those sensitive to HA1004, as the inhibitors differentially regulate the kinetics of Nur77 nuclear import, and FK506, unlike HA1004, inhibits Nur77 DNA-binding activity. Tacrolimus 75-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 16051191-3 2005 We show that Nur77 could discriminate between calcium signals sensitive to FK506 and those sensitive to HA1004, as the inhibitors differentially regulate the kinetics of Nur77 nuclear import, and FK506, unlike HA1004, inhibits Nur77 DNA-binding activity. N-(2-guanidinoethyl)-5-isoquinolinesulfonamide 104-110 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 16009706-3 2005 Substitutions at the 2-position (Cl or CF3) did not alter inhibitory activity, whereas N10-substitutions with derivatives having acetyl (20B) or morpholino (12B) side chain lost activity compared with propyl or butyl substituents (7B and 14B). Morpholinos 145-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-90 16051191-3 2005 We show that Nur77 could discriminate between calcium signals sensitive to FK506 and those sensitive to HA1004, as the inhibitors differentially regulate the kinetics of Nur77 nuclear import, and FK506, unlike HA1004, inhibits Nur77 DNA-binding activity. Tacrolimus 196-201 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 16013898-5 2005 In the modafinil (N = 10) and placebo (N = 10) groups, fatigue improved significantly over time (p < .01), but there were no differences between groups on changes in fatigue, positive and negative symptoms, or cognition. Modafinil 7-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-24 15956351-3 2005 Recently, we found that the purine antimetabolite 6-Mercaptopurine (6-MP), which is widely used as an anti-neoplastic and anti-inflammatory drug, modulated the NR4A1-3 subfamily. purine 28-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-165 16002533-9 2005 The corepressor SMRT interacted with SF-1 in the presence of AII and with nur77 in cells treated with forskolin. Colforsin 102-111 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-79 16002533-6 2005 In the H295R adrenal tumour cell line, SF-1 and nur77 transcripts were increased in cells in the presence of forskolin, whereas nur77 mRNA was also induced with angiotensin II (AII). Colforsin 109-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-53 15956351-3 2005 Recently, we found that the purine antimetabolite 6-Mercaptopurine (6-MP), which is widely used as an anti-neoplastic and anti-inflammatory drug, modulated the NR4A1-3 subfamily. Mercaptopurine 50-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-165 15956351-3 2005 Recently, we found that the purine antimetabolite 6-Mercaptopurine (6-MP), which is widely used as an anti-neoplastic and anti-inflammatory drug, modulated the NR4A1-3 subfamily. Mercaptopurine 68-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-165 15896025-3 2005 In the mixed system, DM is identified to be the "active" component and NP-10 is the "passive" one for the process of adsorption on alumina, while their roles are reversed for silica. Aluminum Oxide 131-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-76 15984106-1 2005 (1) After surgical excision of hormone-receptor-positive non metastatic breast cancer in postmenopausal women, a meta-analysis of 55 trials has shown that adjuvant tamoxifen, 20 mg/day for 5 years, reduces the risk of relapse by 8% and the risk of death by 5% (absolute values). Tamoxifen 164-173 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-47 15984106-11 2005 (5) Pending results of further clinical trials, tamoxifen remains the first-line adjuvant hormone therapy for most postmenopausal women with hormone-receptor-positive non metastatic breast cancer. Tamoxifen 48-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 141-157 15865850-0 2005 Effectiveness and tolerability of fulvestrant in postmenopausal women with hormone receptor-positive breast cancer. Fulvestrant 34-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-91 16833683-7 2005 This provides a framework to interpret the differences observed in the TR3 spectral and triplet lifetime obtained in the neat MeCN solvent (attributed to the free MAP triplet state) and the 50% H2O/50% MeCN solvent (due to the triplet of the hydrogen-bond complex). acetonitrile 126-130 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-74 16833683-7 2005 This provides a framework to interpret the differences observed in the TR3 spectral and triplet lifetime obtained in the neat MeCN solvent (attributed to the free MAP triplet state) and the 50% H2O/50% MeCN solvent (due to the triplet of the hydrogen-bond complex). Water 194-197 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-74 16833683-7 2005 This provides a framework to interpret the differences observed in the TR3 spectral and triplet lifetime obtained in the neat MeCN solvent (attributed to the free MAP triplet state) and the 50% H2O/50% MeCN solvent (due to the triplet of the hydrogen-bond complex). acetonitrile 202-206 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-74 16833683-7 2005 This provides a framework to interpret the differences observed in the TR3 spectral and triplet lifetime obtained in the neat MeCN solvent (attributed to the free MAP triplet state) and the 50% H2O/50% MeCN solvent (due to the triplet of the hydrogen-bond complex). Hydrogen 242-250 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-74 15767262-3 2005 We show that Rb and the related proteins p107 and p130 enhance the activity of NRs related to NGFI-B (Nur factors) through direct interactions with NGFI-B and SRC-2. Rubidium 13-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-100 15767262-3 2005 We show that Rb and the related proteins p107 and p130 enhance the activity of NRs related to NGFI-B (Nur factors) through direct interactions with NGFI-B and SRC-2. Rubidium 13-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 148-154 15716272-6 2005 Similarly, mutation of Met414 in helix 3 to leucine or of Leu591 in helix 12 to isoleucine (the corresponding residues found in NGFI-B) significantly affects Nurr1 transactivation. Isoleucine 80-90 nuclear receptor subfamily 4 group A member 1 Homo sapiens 128-134 15865850-7 2005 In light of the results of comparative phase III trials, fulvestrant is effective and well tolerated in the treatment of postmenopausal women with hormone receptor-positive advanced-stage breast cancer. Fulvestrant 57-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 147-163 15615861-11 2005 Therefore, our data suggest that the NGFI-B may play a significant role in up-regulation of HSD3B2 that leads to the increase in progesterone production that is seen in granulosa cells at ovulation. Progesterone 129-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-43 15625237-7 2005 Nur77 and SHP competitively bound to cAMP response element-binding protein-binding protein and the expression of coactivators, such as cAMP response element-binding protein-binding protein and activating signal cointegrator-2, recovered the decreased function of Nur77 caused by SHP. Cyclic AMP 37-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 15625237-7 2005 Nur77 and SHP competitively bound to cAMP response element-binding protein-binding protein and the expression of coactivators, such as cAMP response element-binding protein-binding protein and activating signal cointegrator-2, recovered the decreased function of Nur77 caused by SHP. Cyclic AMP 37-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 263-268 15625237-7 2005 Nur77 and SHP competitively bound to cAMP response element-binding protein-binding protein and the expression of coactivators, such as cAMP response element-binding protein-binding protein and activating signal cointegrator-2, recovered the decreased function of Nur77 caused by SHP. Cyclic AMP 135-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 15625237-7 2005 Nur77 and SHP competitively bound to cAMP response element-binding protein-binding protein and the expression of coactivators, such as cAMP response element-binding protein-binding protein and activating signal cointegrator-2, recovered the decreased function of Nur77 caused by SHP. Cyclic AMP 135-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 263-268 15767916-12 2005 Hormone therapy with progestogens (hormone receptor expression of the tumor is 71% for estrogens and 95% for progesterone) is widely studied in the literature with a 46% response rate and 46% rate of disease stabilization. Progesterone 109-121 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-51 15615861-4 2005 Real-time RT-PCR was used to quantify mRNA expression levels of the NGFI-B family members in human ovarian follicles, corpora lutea and in human granulosa cells after FSH, phorbol ester (TPA) and forskolin treatment. Phorbol Esters 172-185 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-74 15615861-4 2005 Real-time RT-PCR was used to quantify mRNA expression levels of the NGFI-B family members in human ovarian follicles, corpora lutea and in human granulosa cells after FSH, phorbol ester (TPA) and forskolin treatment. Tetradecanoylphorbol Acetate 187-190 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-74 15615861-4 2005 Real-time RT-PCR was used to quantify mRNA expression levels of the NGFI-B family members in human ovarian follicles, corpora lutea and in human granulosa cells after FSH, phorbol ester (TPA) and forskolin treatment. Colforsin 196-205 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-74 15615861-6 2005 In human granulosa tumour (HGT) cells, the NGFI-B expression increased after TPA, and to a lesser extent, after forskolin treatment. Tetradecanoylphorbol Acetate 77-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-49 15615861-6 2005 In human granulosa tumour (HGT) cells, the NGFI-B expression increased after TPA, and to a lesser extent, after forskolin treatment. Colforsin 112-121 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-49 15615861-7 2005 Treatment of primary cultures of human granulosa cells with forskolin and FSH rapidly increased the NGFI-B mRNA levels followed by an increase in 3beta-hydroxysteroid dehydrogenase type 2 (HSD3B2). Colforsin 60-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 100-106 15668953-0 2005 Determination of threshold values for determining the size of the fraction of steroid hormone receptor-positive tumor cells in paraffin-embedded breast carcinomas. Paraffin 127-135 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-102 15668953-1 2005 BACKGROUND: For 4 years we used a multiparameter DNA flow cytometric (MP-FCM) technique to assess steroid hormone receptor expression in the diagnostic workup of routinely processed formalin-fixed, paraffin-embedded breast carcinomas as an alternative to immunohistochemistry (IHC) for the quantification of hormone receptor-positive cells. Formaldehyde 182-190 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-122 15668953-1 2005 BACKGROUND: For 4 years we used a multiparameter DNA flow cytometric (MP-FCM) technique to assess steroid hormone receptor expression in the diagnostic workup of routinely processed formalin-fixed, paraffin-embedded breast carcinomas as an alternative to immunohistochemistry (IHC) for the quantification of hormone receptor-positive cells. Paraffin 198-206 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-122 15713533-5 2005 Deletion studies of cells stably transfected with truncated hMR indicated that the N-terminal and the DNA binding domains of hMR are essential for enhancement of the catecholamine signal transduction pathway. Catecholamines 166-179 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-63 15713533-5 2005 Deletion studies of cells stably transfected with truncated hMR indicated that the N-terminal and the DNA binding domains of hMR are essential for enhancement of the catecholamine signal transduction pathway. Catecholamines 166-179 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-128 15713533-6 2005 In conclusion, our findings suggest a novel interplay between cAMP and MR signaling pathways. Cyclic AMP 62-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-73 15813510-0 2005 Preclinical and clinical experience with fulvestrant (Faslodex) in postmenopausal women with hormone receptor-positive advanced breast cancer. Fulvestrant 41-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-109 16198055-1 2005 This paper outlines the development of fulvestrant, the first in a new class of antioestrogen agents with no agonist effects, to be used for the treatment of hormone receptor-positive advanced breast cancer in postmenopausal women. Fulvestrant 39-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 158-174 15813510-0 2005 Preclinical and clinical experience with fulvestrant (Faslodex) in postmenopausal women with hormone receptor-positive advanced breast cancer. Fulvestrant 54-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-109 15586024-9 2005 Furthermore, recent studies demonstrating the effect of isoflavones on prostate-specific antigen, testosterone, estrogen, and hormone receptor expression in human subjects will be reviewed. Isoflavones 56-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-142 16203663-6 2005 It is well established that tamoxifen, a selective estrogen receptor modulator (SERM), improves overall survival (OS) in women with hormone receptor (HR) positive breast cancer. Tamoxifen 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-148 16203663-6 2005 It is well established that tamoxifen, a selective estrogen receptor modulator (SERM), improves overall survival (OS) in women with hormone receptor (HR) positive breast cancer. Tamoxifen 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-152 15632249-2 2005 Here we discuss the influence of clinical trial results from the Arimidex, Tamoxifen Alone or in Combination trial on the usage of tamoxifen and anastrozole in the treatment of postmenopausal women with hormone receptor-positive early breast cancer. Anastrozole 65-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 203-219 15486232-7 2005 Interestingly, ectopic expression of NURR1 or NGFI-B severely attenuated the cAMP-responsive activation of the ovary-specific aromatase promoter. Cyclic AMP 77-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-52 15486232-9 2005 The cis-elements responsible for NURR1/NGFI-B-mediated repression were mapped to the minimal aromatase promoter sequence that confers camp responsiveness. Cyclic AMP 134-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-45 15632249-2 2005 Here we discuss the influence of clinical trial results from the Arimidex, Tamoxifen Alone or in Combination trial on the usage of tamoxifen and anastrozole in the treatment of postmenopausal women with hormone receptor-positive early breast cancer. Tamoxifen 75-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 203-219 15632249-2 2005 Here we discuss the influence of clinical trial results from the Arimidex, Tamoxifen Alone or in Combination trial on the usage of tamoxifen and anastrozole in the treatment of postmenopausal women with hormone receptor-positive early breast cancer. Tamoxifen 131-140 nuclear receptor subfamily 4 group A member 1 Homo sapiens 203-219 15632249-2 2005 Here we discuss the influence of clinical trial results from the Arimidex, Tamoxifen Alone or in Combination trial on the usage of tamoxifen and anastrozole in the treatment of postmenopausal women with hormone receptor-positive early breast cancer. Anastrozole 145-156 nuclear receptor subfamily 4 group A member 1 Homo sapiens 203-219 15456750-6 2004 Intrinsic fluorescence of a tryptophan at residue 698 (Trp-698) in the most N-terminal motif was cooperatively quenched by the addition of Ca2+ to Asn-700 Tr2, Tr3, and Tr4 constructs. Tryptophan 28-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-163 15456750-6 2004 Intrinsic fluorescence of a tryptophan at residue 698 (Trp-698) in the most N-terminal motif was cooperatively quenched by the addition of Ca2+ to Asn-700 Tr2, Tr3, and Tr4 constructs. Tryptophan 55-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-163 15456750-7 2004 In Ser-700 constructs, quenching of Trp-698 was incomplete in the Tr2 and Tr3 constructs and complete only in the Tr4 construct. Tryptophan 36-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-77 15506748-7 2004 Our TR3 data reveal that upon ferrous cyt c photoexcitation, (i) distal Met side chain is instantly released, producing a five-coordinated domed heme structure, (ii) proximal His side chain, coupled to the heme, exhibits distortion due to strain exerted by the protein, and (iii) alteration in heme-cysteine coupling takes place along with the relaxation of the protein-induced deformations of the heme macrocycle. Cysteine 299-307 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 15601544-0 2004 [Translocation of orphan receptor TR3 from nuclei to mitochondria induced by staurosporine]. Staurosporine 77-90 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-37 15601544-4 2004 This study was to investigate the mechanism by which STS induces apoptosis of gastric cancer cell line BGC-823,and its correlation with translocation of TR3 in BGC-823 cells. Staurosporine 53-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-156 15319449-9 2004 Moreover, CREB-Nur77 interaction was increased by CREB phosphorylation at Ser-133 and the dominant-negative mutant CREB-M1 efficiently inhibited the synergistic LIF-CRH response. Serine 74-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-20 15319449-11 2004 We conclude that both CREB phosphorylation at Ser-133 and level of CREB expression are crucial in LIF-CRH synergism where CREB, without direct DNA binding, could improve the stability of Nur77 and STAT1-3 binding to POMC promoter and facilitate the recruitment of coactivators. Serine 46-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 187-192 15506748-5 2004 The Fe-His stretching mode at 216 cm-1 has been observed in photoproduct TR3 spectra for the first time for a c-type heme. fe-his 4-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 73-76 15506748-5 2004 The Fe-His stretching mode at 216 cm-1 has been observed in photoproduct TR3 spectra for the first time for a c-type heme. Heme 117-121 nuclear receptor subfamily 4 group A member 1 Homo sapiens 73-76 15506748-7 2004 Our TR3 data reveal that upon ferrous cyt c photoexcitation, (i) distal Met side chain is instantly released, producing a five-coordinated domed heme structure, (ii) proximal His side chain, coupled to the heme, exhibits distortion due to strain exerted by the protein, and (iii) alteration in heme-cysteine coupling takes place along with the relaxation of the protein-induced deformations of the heme macrocycle. Heme 145-149 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 15506748-7 2004 Our TR3 data reveal that upon ferrous cyt c photoexcitation, (i) distal Met side chain is instantly released, producing a five-coordinated domed heme structure, (ii) proximal His side chain, coupled to the heme, exhibits distortion due to strain exerted by the protein, and (iii) alteration in heme-cysteine coupling takes place along with the relaxation of the protein-induced deformations of the heme macrocycle. Heme 206-210 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 15506748-7 2004 Our TR3 data reveal that upon ferrous cyt c photoexcitation, (i) distal Met side chain is instantly released, producing a five-coordinated domed heme structure, (ii) proximal His side chain, coupled to the heme, exhibits distortion due to strain exerted by the protein, and (iii) alteration in heme-cysteine coupling takes place along with the relaxation of the protein-induced deformations of the heme macrocycle. Heme 206-210 nuclear receptor subfamily 4 group A member 1 Homo sapiens 4-7 15666798-0 2004 NGFI-B is important for induction of SF-1 dependent transcription in response to cAMP. Cyclic AMP 81-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-6 15317822-5 2004 The MLN944 molecule adopts a significantly unexpected conformation and side chain orientation in the DNA complex, with the N10 on the phenazine ring protonated at pH 7. phenazine 134-143 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-126 15378476-10 2004 CONCLUSIONS: Current data support anastrozole as first-line adjuvant hormonal therapy, or a change to AIs after 2-3 years of tamoxifen, or the use of letrozole at the end of a 5-year course of tamoxifen as first-choice treatment options for the management of hormone receptor-positive breast carcinoma in postmenopausal women. Anastrozole 34-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 259-275 15476902-11 2004 RESULTS: Anastrozole, letrozole, and exemestane are the 3 commercially available aromatase inhibitors approved by the US Food and Drug Administration for the treatment of hormone receptor-positive breast cancer in postmenopausal women. Anastrozole 9-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-187 15387586-1 2004 Pico- and nanosecond time-resolved resonance Raman (TR3) spectroscopy have been utilized to study the dynamics and structure of p-hydroxyacetophenone (HA) and the p-hydroxyphenacyl-caged phototrigger compound p-hydroxyphenacyl diethyl phosphate (HPDP) in acetonitrile solution. 4-hydroxyacetophenone 128-149 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-55 15208301-11 2004 Infection of cultured human adrenal cells with adenovirus-containing NGFIB increased cortisol production by 8-fold and increased expression of HSD3B2 mRNA 26-fold over that observed in mock-infected cells. Hydrocortisone 85-93 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-74 15347434-1 2004 Tamoxifen is currently a standard of care for postmenopausal patients with breast cancer with hormone receptor-positive tumors who are candidates for adjuvant endocrine therapy. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-110 15347435-6 2004 The results of 2 large adjuvant trials using AIs sequentially with tamoxifen in postmenopausal women with early-stage, HR-positive breast cancer have been reported. Tamoxifen 67-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-121 15387586-1 2004 Pico- and nanosecond time-resolved resonance Raman (TR3) spectroscopy have been utilized to study the dynamics and structure of p-hydroxyacetophenone (HA) and the p-hydroxyphenacyl-caged phototrigger compound p-hydroxyphenacyl diethyl phosphate (HPDP) in acetonitrile solution. 4-hydroxyacetophenone 151-153 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-55 15387586-1 2004 Pico- and nanosecond time-resolved resonance Raman (TR3) spectroscopy have been utilized to study the dynamics and structure of p-hydroxyacetophenone (HA) and the p-hydroxyphenacyl-caged phototrigger compound p-hydroxyphenacyl diethyl phosphate (HPDP) in acetonitrile solution. p-hydroxyphenacyl 163-180 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-55 15342804-7 2004 CONCLUSIONS: As compared with tamoxifen alone, radiotherapy plus tamoxifen significantly reduces the risk of breast and axillary recurrence after lumpectomy in women with small, node-negative, hormone-receptor-positive breast cancers. Tamoxifen 65-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 193-209 15016657-0 2004 Induction of orphan nuclear receptor Nur77 gene expression and its role in cadmium-induced apoptosis in lung. Cadmium 75-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-42 15016657-4 2004 In the present study, we characterized the induction of the Nur77 family genes in the lungs after cadmium exposure. Cadmium 98-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-65 15016657-5 2004 Nur77, Nor-1 and Nurr1 were all induced after cadmium treatment in a dose- and time-dependent manner in WI-38 and A549 lung cell lines. Cadmium 46-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 15016657-6 2004 Treatment with inhibitors of signaling pathways, such as PD98059 and H89, almost completely blocked the expression of Nur77, indicating that the extracellular signal-regulated kinase and protein kinase A signaling pathways are important in cadmium-induced Nur77 expression. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 57-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 15016657-6 2004 Treatment with inhibitors of signaling pathways, such as PD98059 and H89, almost completely blocked the expression of Nur77, indicating that the extracellular signal-regulated kinase and protein kinase A signaling pathways are important in cadmium-induced Nur77 expression. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 57-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 256-261 15016657-6 2004 Treatment with inhibitors of signaling pathways, such as PD98059 and H89, almost completely blocked the expression of Nur77, indicating that the extracellular signal-regulated kinase and protein kinase A signaling pathways are important in cadmium-induced Nur77 expression. Cadmium 240-247 nuclear receptor subfamily 4 group A member 1 Homo sapiens 118-123 15016657-6 2004 Treatment with inhibitors of signaling pathways, such as PD98059 and H89, almost completely blocked the expression of Nur77, indicating that the extracellular signal-regulated kinase and protein kinase A signaling pathways are important in cadmium-induced Nur77 expression. Cadmium 240-247 nuclear receptor subfamily 4 group A member 1 Homo sapiens 256-261 15016657-7 2004 When a plasmid encoding dominant-negative Nur77 was transfected into A549 cells, cadmium-induced apoptotic changes, such as chromosomal condensation and Bax expression, were significantly reduced, suggesting that the expression of Nur77 plays an important role in cadmium-induced apoptosis. Cadmium 81-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-47 15016657-7 2004 When a plasmid encoding dominant-negative Nur77 was transfected into A549 cells, cadmium-induced apoptotic changes, such as chromosomal condensation and Bax expression, were significantly reduced, suggesting that the expression of Nur77 plays an important role in cadmium-induced apoptosis. Cadmium 81-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 231-236 15016657-7 2004 When a plasmid encoding dominant-negative Nur77 was transfected into A549 cells, cadmium-induced apoptotic changes, such as chromosomal condensation and Bax expression, were significantly reduced, suggesting that the expression of Nur77 plays an important role in cadmium-induced apoptosis. Cadmium 264-271 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-47 15016657-7 2004 When a plasmid encoding dominant-negative Nur77 was transfected into A549 cells, cadmium-induced apoptotic changes, such as chromosomal condensation and Bax expression, were significantly reduced, suggesting that the expression of Nur77 plays an important role in cadmium-induced apoptosis. Cadmium 264-271 nuclear receptor subfamily 4 group A member 1 Homo sapiens 231-236 15016657-9 2004 Taken together, these results demonstrate that cadmium induces the expression of Nur77 family genes, leading to apoptosis in lung cells, which may cause pulmonary toxicity in response to cadmium exposure. Cadmium 47-54 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-86 15016657-9 2004 Taken together, these results demonstrate that cadmium induces the expression of Nur77 family genes, leading to apoptosis in lung cells, which may cause pulmonary toxicity in response to cadmium exposure. Cadmium 187-194 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-86 15476902-11 2004 RESULTS: Anastrozole, letrozole, and exemestane are the 3 commercially available aromatase inhibitors approved by the US Food and Drug Administration for the treatment of hormone receptor-positive breast cancer in postmenopausal women. Letrozole 22-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-187 15476902-11 2004 RESULTS: Anastrozole, letrozole, and exemestane are the 3 commercially available aromatase inhibitors approved by the US Food and Drug Administration for the treatment of hormone receptor-positive breast cancer in postmenopausal women. exemestane 37-47 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-187 15159280-0 2004 Upregulation of orphan nuclear receptor Nur77 following PGF(2alpha), Bimatoprost, and Butaprost treatments. Prostaglandins F 56-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-45 15159280-0 2004 Upregulation of orphan nuclear receptor Nur77 following PGF(2alpha), Bimatoprost, and Butaprost treatments. Bimatoprost 69-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-45 15159280-10 2004 We also used Nur77 as a marker gene to compare the effects of PGF(2alpha), Butaprost, and Bimatoprost (a prostamide) on Nur77 expression in human primary trabecular meshwork and ciliary smooth muscle (SM) cells, which are target cells for antiglaucoma drugs. Prostaglandins F 62-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-125 15159280-0 2004 Upregulation of orphan nuclear receptor Nur77 following PGF(2alpha), Bimatoprost, and Butaprost treatments. butaprost 86-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-45 15159280-10 2004 We also used Nur77 as a marker gene to compare the effects of PGF(2alpha), Butaprost, and Bimatoprost (a prostamide) on Nur77 expression in human primary trabecular meshwork and ciliary smooth muscle (SM) cells, which are target cells for antiglaucoma drugs. butaprost 75-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-125 15159280-10 2004 We also used Nur77 as a marker gene to compare the effects of PGF(2alpha), Butaprost, and Bimatoprost (a prostamide) on Nur77 expression in human primary trabecular meshwork and ciliary smooth muscle (SM) cells, which are target cells for antiglaucoma drugs. Bimatoprost 90-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-125 15159280-11 2004 The results showed that PGF(2alpha) and Butaprost, but not Bimatoprost, induced upregulation of Nur77 expression in human TM cells. Prostaglandins F 24-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-101 15159280-3 2004 Using gene chip technology, we first identified that PGF(2alpha) (FP agonist) and Butaprost (EP(2) agonist) induced about a five-fold upregulation of Nur77 mRNA expression in hFP-HEK 293/EBNA and hEP(2)-HEK293/EBNA cells. Prostaglandins F 53-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-155 15159280-11 2004 The results showed that PGF(2alpha) and Butaprost, but not Bimatoprost, induced upregulation of Nur77 expression in human TM cells. butaprost 40-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-101 15159280-3 2004 Using gene chip technology, we first identified that PGF(2alpha) (FP agonist) and Butaprost (EP(2) agonist) induced about a five-fold upregulation of Nur77 mRNA expression in hFP-HEK 293/EBNA and hEP(2)-HEK293/EBNA cells. butaprost 82-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-155 15159280-12 2004 PGF(2alpha), but not Bimatoprost, dramatically induced upregulation of Nur77 mRNA expression in human ciliary SM cells, whereas Butaprost slightly upregulated Nur77 mRNA expression in SM cells. Prostaglandins F 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-76 15159280-12 2004 PGF(2alpha), but not Bimatoprost, dramatically induced upregulation of Nur77 mRNA expression in human ciliary SM cells, whereas Butaprost slightly upregulated Nur77 mRNA expression in SM cells. butaprost 128-137 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-164 15159280-4 2004 Northern Blot analysis revealed that PGF(2alpha)- and Butaprost-induced upregulation of Nur77 expression are dose- and time-dependent. Prostaglandins F 37-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-93 15159280-14 2004 Nur77 promoter deletion analysis indicated that PGF(2alpha), but not Bimatoprost, activated Nur77 promoter-luciferase reporter in hFP-HEK 293/EBNA cells. Prostaglandins F 48-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 15159280-4 2004 Northern Blot analysis revealed that PGF(2alpha)- and Butaprost-induced upregulation of Nur77 expression are dose- and time-dependent. butaprost 54-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-93 15159280-14 2004 Nur77 promoter deletion analysis indicated that PGF(2alpha), but not Bimatoprost, activated Nur77 promoter-luciferase reporter in hFP-HEK 293/EBNA cells. Prostaglandins F 48-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-97 15159280-15 2004 Butaprost was less efficacious in inducing Nur77 promoter-luciferase reporter activity in hEP(2)-HEK293/EBNA cells relative to PGF(2alpha) in the comparable assay. butaprost 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-48 15159280-6 2004 Both PGF(2alpha) and Butaprost upregulated Nur77 gene expression through the protein kinase C (PKC) pathway. Prostaglandins F 5-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-48 15159280-18 2004 It appears that PGF(2alpha) and Butaprost activate Nur77 transcription mechanisms through the activation of FP and EP(2) receptor-coupled signaling pathways, whereas Bimatoprost stimulates neither FP nor EP(2) receptors. Prostaglandins F 16-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-56 15159280-6 2004 Both PGF(2alpha) and Butaprost upregulated Nur77 gene expression through the protein kinase C (PKC) pathway. butaprost 21-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-48 15159280-18 2004 It appears that PGF(2alpha) and Butaprost activate Nur77 transcription mechanisms through the activation of FP and EP(2) receptor-coupled signaling pathways, whereas Bimatoprost stimulates neither FP nor EP(2) receptors. butaprost 32-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-56 15193263-2 2004 Here, we generated gene expression profiles of hormone receptor-positive primary breast cancers in a set of 60 patients treated with adjuvant tamoxifen monotherapy. Tamoxifen 142-151 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-63 15159280-8 2004 Calcineurin was found to be involved downstream of the PKC pathway in PGF(2alpha)-induced Nur77 expression, but not in Butaprost-induced Nur77 expression. Prostaglandins F 70-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-95 15128284-10 2004 Increased protein expression of nur77 and the greatest binding of nur77 to its response element was seen when cells were stimulated with A-II in combination with forskolin. Colforsin 162-171 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-37 15125747-5 2004 A relationship between objective response rate (complete or partial response) or clinical benefit (complete or partial response or stabilization for > or =24 weeks) and hormone receptor status was apparent for anastrozole but not letrozole treatment. Anastrozole 213-224 nuclear receptor subfamily 4 group A member 1 Homo sapiens 172-188 15128284-10 2004 Increased protein expression of nur77 and the greatest binding of nur77 to its response element was seen when cells were stimulated with A-II in combination with forskolin. Colforsin 162-171 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-71 15128284-11 2004 These data indicate that nur77 may preferentially regulate steroid enzyme genes relevant to cortisol production and thereby regulate differential cortisol and adrenal androgen production. Steroids 59-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 25-30 15134811-1 2004 The human mineralocorticoid receptor (hMR), a ligand-dependent transcription factor (NR3C2) which belongs to the nuclear receptor superfamily, mediates most of the known effects of aldosterone. Aldosterone 181-192 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-41 14645496-0 2004 The orphan nuclear receptors NURR1 and NGFIB regulate adrenal aldosterone production. Aldosterone 62-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 14766275-3 2004 METHODS: Microarray-based expression profiling was performed on a series of tamoxifen-associated (N = 10) and matched sporadic cases (N = 29) of endometrial carcinoma. Tamoxifen 76-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 98-104 14729605-8 2004 The treatment of Nur77 antisense oligonucleotide reduces POMC transcription under hypoxic conditions. Oligonucleotides 33-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-22 14703069-6 2003 In patients with confirmed hormone receptor (HR)-positive tumors, the CB rate was 51.9 and 65.7%, respectively, for anastrozole and 41.6 and 58.7%, respectively, for tamoxifen. Anastrozole 116-127 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-43 14592536-0 2004 Distinct role and functional mode of TR3 and RARalpha in mediating ATRA-induced signalling pathway in breast and gastric cancer cells. Tretinoin 67-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-40 14592536-4 2004 In the present study, we found that formation of TR3/RXRalpha heterodimers in the nucleus and their subsequent translocation into the cytoplasm, in association with regulation of apoptosis-related proteins Bcl-2, Bcl-xl and Bax, was critical for apoptosis induction by ATRA in breast cancer cells MCF-7. Tretinoin 269-273 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-52 14592536-8 2004 Furthermore, we demonstrated that the effects of ATRA depend on the relative levels of TR3, RARalpha and RXRalpha expression in cancer cells. Tretinoin 49-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-90 14592536-9 2004 In ATRA-induced MCF-7 cells, highly expressed TR3 favours the formation of TR3/RXRalpha and promotes the TR3/RXRalpha signalling pathway causing apoptosis; while in ATRA-induced MGC80-3 cells, high expression of RARalpha favours the formation of RARalpha/RXRalpha and promotes the RXRalpha/RARalpha signalling pathway in mediating cell cycle regulation. Tretinoin 3-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-49 14592536-9 2004 In ATRA-induced MCF-7 cells, highly expressed TR3 favours the formation of TR3/RXRalpha and promotes the TR3/RXRalpha signalling pathway causing apoptosis; while in ATRA-induced MGC80-3 cells, high expression of RARalpha favours the formation of RARalpha/RXRalpha and promotes the RXRalpha/RARalpha signalling pathway in mediating cell cycle regulation. Tretinoin 3-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-78 14592536-9 2004 In ATRA-induced MCF-7 cells, highly expressed TR3 favours the formation of TR3/RXRalpha and promotes the TR3/RXRalpha signalling pathway causing apoptosis; while in ATRA-induced MGC80-3 cells, high expression of RARalpha favours the formation of RARalpha/RXRalpha and promotes the RXRalpha/RARalpha signalling pathway in mediating cell cycle regulation. Tretinoin 3-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-78 15033715-0 2003 Orphan nuclear receptor Nur77 translocates to mitochondria in the early phase of apoptosis induced by synthetic chenodeoxycholic acid derivatives in human stomach cancer cell line SNU-1. Chenodeoxycholic Acid 112-133 nuclear receptor subfamily 4 group A member 1 Homo sapiens 24-29 15033715-3 2003 Importantly, the orphan receptor Nur77 (TR3) was shown to translocate from the nucleus to mitochondria at the early time points after CDCA derivatives treatment. Chenodeoxycholic Acid 134-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 33-38 15033715-3 2003 Importantly, the orphan receptor Nur77 (TR3) was shown to translocate from the nucleus to mitochondria at the early time points after CDCA derivatives treatment. Chenodeoxycholic Acid 134-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-43 15033715-4 2003 These data support the theory that CDCA derivatives-induced apoptosis of SNU-1 gastric cancer cell lines is mediated by mitochondria and caspase, and, at least in part, by Nur77. Chenodeoxycholic Acid 35-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 172-177 14734491-9 2004 Anastrozole should, therefore, now be considered a valid alternative option to tamoxifen for adjuvant hormonal treatment in all postmenopausal women with hormone receptor-positive early breast cancer. Anastrozole 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 154-170 14703069-6 2003 In patients with confirmed hormone receptor (HR)-positive tumors, the CB rate was 51.9 and 65.7%, respectively, for anastrozole and 41.6 and 58.7%, respectively, for tamoxifen. Anastrozole 116-127 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-47 14703069-6 2003 In patients with confirmed hormone receptor (HR)-positive tumors, the CB rate was 51.9 and 65.7%, respectively, for anastrozole and 41.6 and 58.7%, respectively, for tamoxifen. Tamoxifen 166-175 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-43 14703069-6 2003 In patients with confirmed hormone receptor (HR)-positive tumors, the CB rate was 51.9 and 65.7%, respectively, for anastrozole and 41.6 and 58.7%, respectively, for tamoxifen. Tamoxifen 166-175 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-47 12947120-3 2003 Here we found that 12-O-tetradecanoylphorbol-13-acetate (TPA) could induce cell apoptosis via induction of TR3 and E2F1 expression in LNCaP prostate cancer cells. Tetradecanoylphorbol Acetate 19-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-110 14525795-8 2003 VEGF increased protein expression of Nurr1 and Nur77 and decreased Nur77 phosphorylation at the negative regulatory site serine 351. Serine 121-127 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-72 12947120-5 2003 These data suggest that TPA is able to induce LNCaP cell apoptosis via induction of TR3 resulting in the induction of E2F1. Tetradecanoylphorbol Acetate 24-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-87 12947120-3 2003 Here we found that 12-O-tetradecanoylphorbol-13-acetate (TPA) could induce cell apoptosis via induction of TR3 and E2F1 expression in LNCaP prostate cancer cells. Tetradecanoylphorbol Acetate 57-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 107-110 12947120-8 2003 Taken together, these data suggest that TPA is able to induce cell apoptosis via a TPA --> TR3 --> E2F1 --> apoptosis pathway in LNCaP cells. Tetradecanoylphorbol Acetate 40-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-97 12947120-8 2003 Taken together, these data suggest that TPA is able to induce cell apoptosis via a TPA --> TR3 --> E2F1 --> apoptosis pathway in LNCaP cells. Tetradecanoylphorbol Acetate 83-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-97 14535708-1 2003 [reaction: see text] Biotin was conjugated to chemiluminescent N-sulfonylacridinium-9-carboxamides at the N-10 or 9-position carboxamide. Biotin 21-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-110 14535708-1 2003 [reaction: see text] Biotin was conjugated to chemiluminescent N-sulfonylacridinium-9-carboxamides at the N-10 or 9-position carboxamide. n-sulfonylacridinium-9-carboxamides 63-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-110 14535708-1 2003 [reaction: see text] Biotin was conjugated to chemiluminescent N-sulfonylacridinium-9-carboxamides at the N-10 or 9-position carboxamide. carboxamide 86-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-110 14535708-2 2003 Upon binding to avidin, the light output of the N-10 derivative (8) was quenched up to 92% upon triggering with basic peroxide, while the 9-position carboxamide conjugate (9) was quenched only 33%. Peroxides 118-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 48-52 14587704-1 2003 Picosecond time-resolved resonance Raman spectroscopy, TR3, reveals an intense acetylenic band in the S1 state of the prototypical molecular wire 1,4-bis(phenylethynyl)benzene. 1,4-Bis(phenylethynyl)benzene 146-175 nuclear receptor subfamily 4 group A member 1 Homo sapiens 55-58 12974624-7 2003 The crystal structure suggests that a buried Lys(267) is transiently protonated during formyl transfer allowing for the stabilization of the oxyanion transition state and subsequent protonation of N10 on the tetrahydrofolate leaving group. Lysine 45-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 197-200 14578143-8 2003 Alcohol use appears to be more strongly associated with risk of lobular carcinomas and hormone receptor-positive tumors than it is with other types of breast cancer. Alcohols 0-7 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-103 12974624-7 2003 The crystal structure suggests that a buried Lys(267) is transiently protonated during formyl transfer allowing for the stabilization of the oxyanion transition state and subsequent protonation of N10 on the tetrahydrofolate leaving group. 5,6,7,8-tetrahydrofolic acid 208-224 nuclear receptor subfamily 4 group A member 1 Homo sapiens 197-200 14500374-4 2003 Nucleus-to-cytoplasm translocation of a green fluorescent protein-TR3 construct, but not its direct mitochondrial targeting, was associated with apoptosis induced by the short-chain fatty acid, butyrate. Fatty Acids, Volatile 170-192 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-69 12842839-5 2003 Adenoviral overexpression of TR3 in cultured endothelial cells resulted in decreased [3H]thymidine incorporation, whereas a dominant-negative TR3 variant that inhibits the activity of endogenous TR3-like factors enhanced DNA synthesis. Tritium 86-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-32 12842839-5 2003 Adenoviral overexpression of TR3 in cultured endothelial cells resulted in decreased [3H]thymidine incorporation, whereas a dominant-negative TR3 variant that inhibits the activity of endogenous TR3-like factors enhanced DNA synthesis. Thymidine 89-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-32 14500374-4 2003 Nucleus-to-cytoplasm translocation of a green fluorescent protein-TR3 construct, but not its direct mitochondrial targeting, was associated with apoptosis induced by the short-chain fatty acid, butyrate. Butyrates 194-202 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-69 12791423-2 2003 The use of tamoxifen in women with hormone receptor-positive tumors is a relatively simple therapeutic option considering the favourable toxicity profile, whereas the administration of adjuvant chemotherapy is more complicated and a variety of aspects need to be considered. Tamoxifen 11-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-51 14659138-2 2003 Tamoxifen, a selective estrogen receptor modulator, is the standard endocrine treatment for hormone receptor-positive breast cancer, both in the adjuvant and metastatic settings. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-108 12429630-0 2002 Pattern of hormone receptor status of secondary contralateral breast cancers in patients receiving adjuvant tamoxifen. Tamoxifen 108-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-27 12770726-2 2003 In the rat ovary, the preovulatory surge of LH induces NGFI-B expression in granulosa cells of preovulatory follicles, reaching a peak within 1 h and declining to control levels at 6 h. The LH-stimulated NGFI-B expression is abolished by alpha-amanitin, but superinduced by cycloheximide. Luteinizing Hormone 44-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 204-210 12770726-2 2003 In the rat ovary, the preovulatory surge of LH induces NGFI-B expression in granulosa cells of preovulatory follicles, reaching a peak within 1 h and declining to control levels at 6 h. The LH-stimulated NGFI-B expression is abolished by alpha-amanitin, but superinduced by cycloheximide. Alpha-Amanitin 238-252 nuclear receptor subfamily 4 group A member 1 Homo sapiens 204-210 12770726-2 2003 In the rat ovary, the preovulatory surge of LH induces NGFI-B expression in granulosa cells of preovulatory follicles, reaching a peak within 1 h and declining to control levels at 6 h. The LH-stimulated NGFI-B expression is abolished by alpha-amanitin, but superinduced by cycloheximide. Cycloheximide 274-287 nuclear receptor subfamily 4 group A member 1 Homo sapiens 204-210 12770726-4 2003 Interestingly, the induction of NGFI-B expression in response to LH stimulation in preovulatory granulosa cells requires signaling through protein kinase Czeta. Luteinizing Hormone 65-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-38 12704790-9 2003 Finally, we were able to determine that CD437 treatment induced the translocation of TR3, a nuclear orphan receptor, whereas, 4-HPR did not. CD 437 40-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-88 12429630-2 2002 As a result, only limited data are available on the hormone receptor status of CBCs evolving in tamoxifen-treated patients. Tamoxifen 96-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 52-68 12429630-3 2002 The aim of our investigation was to evaluate the pattern of hormone receptor status of CBCs in patients treated with adjuvant tamoxifen at our institution. Tamoxifen 126-135 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-76 12376465-0 2002 Dual roles of Nur77 in selective regulation of apoptosis and cell cycle by TPA and ATRA in gastric cancer cells. Tetradecanoylphorbol Acetate 75-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-19 12376465-0 2002 Dual roles of Nur77 in selective regulation of apoptosis and cell cycle by TPA and ATRA in gastric cancer cells. Tretinoin 83-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-19 12376465-5 2002 The tetradecanoylphorbol-1,3-acetate (TPA) treatment not only resulted in up-regulation of the Nur77 mRNA level, but also led to translocation of Nur77 protein from the nucleus to the mitochondria, and caused the release of cytochrome c. tetradecanoylphorbol-1,3-acetate 4-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 95-100 12376515-0 2002 Interaction of dietary folate intake, alcohol, and risk of hormone receptor-defined breast cancer in a prospective study of postmenopausal women. Folic Acid 23-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-75 12376465-5 2002 The tetradecanoylphorbol-1,3-acetate (TPA) treatment not only resulted in up-regulation of the Nur77 mRNA level, but also led to translocation of Nur77 protein from the nucleus to the mitochondria, and caused the release of cytochrome c. tetradecanoylphorbol-1,3-acetate 4-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 146-151 12376465-5 2002 The tetradecanoylphorbol-1,3-acetate (TPA) treatment not only resulted in up-regulation of the Nur77 mRNA level, but also led to translocation of Nur77 protein from the nucleus to the mitochondria, and caused the release of cytochrome c. Tetradecanoylphorbol Acetate 38-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 95-100 12376465-5 2002 The tetradecanoylphorbol-1,3-acetate (TPA) treatment not only resulted in up-regulation of the Nur77 mRNA level, but also led to translocation of Nur77 protein from the nucleus to the mitochondria, and caused the release of cytochrome c. Tetradecanoylphorbol Acetate 38-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 146-151 12376465-6 2002 This TPA-induced translocation of Nur77 was in association with the initiation of apoptosis in gastric cancer cells. Tetradecanoylphorbol Acetate 5-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-39 12376465-7 2002 Although all-trans retinoic acid (ATRA) could not induce apoptosis in BGC-823 cells due to failure of stimulating Nur77 translocation, expression of Nur77 in the nucleus was required for cell growth inhibition by ATRA. Tretinoin 213-217 nuclear receptor subfamily 4 group A member 1 Homo sapiens 149-154 12376465-9 2002 Furthermore, the action of Nur77 in TPA-induced apoptosis was mediated through a protein kinase C signaling pathway, while mitogen-activated protein kinase and phosphatidylinositol 3-kinase signaling pathways were responsible for the regulation of Nur77 mRNA expression. Tetradecanoylphorbol Acetate 36-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-32 12376465-10 2002 Taken together, the data revealed the dual functioning mechanisms of Nur77 in gastric cancer cells in response to TPA and ATRA. Tetradecanoylphorbol Acetate 114-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-74 12376465-10 2002 Taken together, the data revealed the dual functioning mechanisms of Nur77 in gastric cancer cells in response to TPA and ATRA. Tretinoin 122-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-74 12401435-3 2002 An alteration in the fatty acid composition of membrane phospholipids could affect critical membrane-dependent enzymes and processes (e.g., ion and solute transport, hormone-receptor interactions, signal transduction pathways). Fatty Acids 21-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-182 12401435-3 2002 An alteration in the fatty acid composition of membrane phospholipids could affect critical membrane-dependent enzymes and processes (e.g., ion and solute transport, hormone-receptor interactions, signal transduction pathways). Phospholipids 56-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-182 12149306-10 2002 A 5-year course of adjuvant tamoxifen remains the standard therapy for women with hormone receptor-positive breast cancer. Tamoxifen 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-98 12071889-6 2002 This is in contrast to the increased sex hormone receptor expressions in all uterine cell types, observed in spontaneously occurring CEH. CEH 133-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 41-57 12089357-0 2002 Activation and induction of NUR77/NURR1 in corticotrophs by CRH/cAMP: involvement of calcium, protein kinase A, and MAPK pathways. Cyclic AMP 64-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 12089357-2 2002 In this study we show that in AtT-20 corticotrophs CRH and cAMP induce Nur77 and Nurr1 expression and transcription at the NurRE site by protein kinase A (PKA) and calcium-dependent and -independent mechanisms. Cyclic AMP 59-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-76 12089357-2 2002 In this study we show that in AtT-20 corticotrophs CRH and cAMP induce Nur77 and Nurr1 expression and transcription at the NurRE site by protein kinase A (PKA) and calcium-dependent and -independent mechanisms. Calcium 164-171 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-76 12089357-9 2002 In conclusion, in AtT-20 corticotrophs the CRH/cAMP signaling that leads to Nur77/Nurr1 mRNA induction and transcriptional activation, and thus POMC expression, is dependent on protein kinase A and involves calcium/calmodulin kinase II (Nur induction/activation) and MAPK calcium-dependent and -independent (Nur phosphorylation-activation) pathways. Cyclic AMP 47-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-81 12089357-9 2002 In conclusion, in AtT-20 corticotrophs the CRH/cAMP signaling that leads to Nur77/Nurr1 mRNA induction and transcriptional activation, and thus POMC expression, is dependent on protein kinase A and involves calcium/calmodulin kinase II (Nur induction/activation) and MAPK calcium-dependent and -independent (Nur phosphorylation-activation) pathways. Calcium 207-214 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-81 11884470-4 2002 Modulation by proinflammatory mediators in primary RA and normal synoviocytes shows that PGE(2), IL-1beta, and TNF-alpha markedly enhance NURR1 mRNA and protein levels in contrast to other subfamily members, NUR77 and NOR-1. Prostaglandins E 89-92 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 11954047-0 2002 Acute methamphetamine administration upregulates NGFI-B mRNA expression in the striatum: co-localization with c-Fos immunoreactivity. Methamphetamine 6-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-55 11954047-1 2002 In this study, the effects of acute methamphetamine administration on expression of the nuclear transcription factor NGFI-B mRNA and its co-localization with c-Fos immunoreactivity in the striatum were evaluated in animals receiving a single dose of methamphetamine (4 mg/kg) given at 2 or 6 h prior to perfusion. Methamphetamine 36-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 117-123 11954047-1 2002 In this study, the effects of acute methamphetamine administration on expression of the nuclear transcription factor NGFI-B mRNA and its co-localization with c-Fos immunoreactivity in the striatum were evaluated in animals receiving a single dose of methamphetamine (4 mg/kg) given at 2 or 6 h prior to perfusion. Methamphetamine 250-265 nuclear receptor subfamily 4 group A member 1 Homo sapiens 117-123 11954047-3 2002 We have found that, similar to c-fos activation, NGFI-B mRNA levels were significantly increased 2 h after methamphetamine treatment and returned to basal levels 6 h later. Methamphetamine 107-122 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-55 11954047-4 2002 Induction of NGFI-B mRNA levels by methamphetamine was highest in central striatum as compared to the dorsomedial distribution pattern observed in control animals. Methamphetamine 35-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-19 11954047-5 2002 After acute methamphetamine treatment, the distribution pattern of NGFI-B mRNA upregulation was very similar to that of methamphetamine induced c-Fos immunoreactivity. Methamphetamine 12-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-73 11954047-8 2002 This study provides a detailed description of the differential spatial and temporal modulation of NGFI-B and c-Fos expression in the striatum by acute methamphetamine treatment over time. Methamphetamine 151-166 nuclear receptor subfamily 4 group A member 1 Homo sapiens 98-104 12095685-4 2002 NGFI-B mRNA and protein expression were promptly (15 min) increased after 8-Br-cAMP treatment and precedes aldolase C mRNA increase (30 min). 8-Bromo Cyclic Adenosine Monophosphate 74-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-6 12095685-5 2002 After 4 h of 8-Br-cAMP treatment, the binding of NGFI-B protein to the distal element D in the distal promoter region was increased twofold and this correlates with the increased expression of the clone that contains distal element D. These results indicate that the distal element D in the promoter region of the human aldolase C gene is the target of a cAMP-dependent regulation pathway. 8-Bromo Cyclic Adenosine Monophosphate 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-55 12095685-5 2002 After 4 h of 8-Br-cAMP treatment, the binding of NGFI-B protein to the distal element D in the distal promoter region was increased twofold and this correlates with the increased expression of the clone that contains distal element D. These results indicate that the distal element D in the promoter region of the human aldolase C gene is the target of a cAMP-dependent regulation pathway. Cyclic AMP 18-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-55 12011136-9 2002 CONCLUSION: Vietnamese and Chinese women with hormone receptor-positive operable breast cancer benefit from adjuvant treatment with surgical oophorectomy and tamoxifen. Tamoxifen 158-167 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-62 11979430-5 2002 The inhibitory effect of nicotine was accompanied with induction of orphan receptor TR3. Nicotine 25-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 84-87 11979430-6 2002 Inhibition of TR3 expression by overexpression of TR3 anti-sense RNA in H460 lung cancer cells strongly prevented the suppressive effect of nicotine on trans-RA activity. Nicotine 140-148 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-17 11979430-6 2002 Inhibition of TR3 expression by overexpression of TR3 anti-sense RNA in H460 lung cancer cells strongly prevented the suppressive effect of nicotine on trans-RA activity. Nicotine 140-148 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-53 11979430-10 2002 Together, our results demonstrate that nicotine suppresses the growth inhibitory effects of trans-RA by inhibiting RAR beta expression through its induction of TR3 expression and suggest that RXR-selective retinoids may be more effective than classical retinoids for preventing and treating tobacco-associated cancers. Nicotine 39-47 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-163 11883936-3 2002 EGF stimulation of cells leads to phosphorylation of threonine in NGFI-B. Threonine 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-72 11883936-4 2002 Thr-142 of NGFI-B is comprised in a consensus MAP kinase site and was identified as a preferred substrate for ERK2 (but not ERK1) in vitro. Threonine 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 11-17 11895893-6 2002 In 1998, letrozole was approved by the United States Food and Drug Administration (FDA) for the treatment of advanced breast cancer in postmenopausal women, with hormone receptor positive or unknown breast cancer, who had failed one prior antiestrogen treatment (i.e., for "second-line" treatment). Letrozole 9-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 162-178 11895893-11 2002 In July 2000, a marketing application for first-line letrozole treatment of postmenopausal women with hormone receptor positive or hormone receptor unknown locally advanced or metastatic breast cancer was submitted to the FDA. Letrozole 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 131-147 11895893-11 2002 In July 2000, a marketing application for first-line letrozole treatment of postmenopausal women with hormone receptor positive or hormone receptor unknown locally advanced or metastatic breast cancer was submitted to the FDA. Letrozole 53-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-118 11895893-18 2002 On the basis of these results, the United States FDA approved letrozole tablets, 2.5 mg/day, for first-line treatment of postmenopausal women with hormone receptor-positive or hormone receptor-unknown locally advanced or metastatic breast cancer. Letrozole 62-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 147-163 11895893-18 2002 On the basis of these results, the United States FDA approved letrozole tablets, 2.5 mg/day, for first-line treatment of postmenopausal women with hormone receptor-positive or hormone receptor-unknown locally advanced or metastatic breast cancer. Letrozole 62-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 176-192 11700033-4 2001 When Chang X-34 expressing HBx under the control of a doxycycline-inducible promoter was examined, induction of Nur77 was observed following HBx expression. Doxycycline 54-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 112-117 11719525-0 2002 A calcium/calmodulin-dependent activation of ERK1/2 mediates JunD phosphorylation and induction of nur77 and 20alpha-hsd genes by prostaglandin F2alpha in ovarian cells. Dinoprost 130-151 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-104 11719525-1 2002 We have previously demonstrated that prostaglandin F(2alpha) (PGF(2alpha)) induces a rapid and transient expression of Nur77 in luteal cells. Prostaglandins F 37-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-124 11719525-1 2002 We have previously demonstrated that prostaglandin F(2alpha) (PGF(2alpha)) induces a rapid and transient expression of Nur77 in luteal cells. Prostaglandins F 62-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-124 11719525-2 2002 We have shown that Nur77 plays an important role in ovarian physiology by mediating the PGF(2alpha) induction of 20alpha-HSD, a steroidogenic enzyme involved in the catabolism of progesterone. Prostaglandins F 88-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-24 11719525-2 2002 We have shown that Nur77 plays an important role in ovarian physiology by mediating the PGF(2alpha) induction of 20alpha-HSD, a steroidogenic enzyme involved in the catabolism of progesterone. Progesterone 179-191 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-24 11719525-3 2002 In this report we established, using luteinized granulosa cells, that PGF(2alpha) stimulates in vitro nur77 expression in a time- and dose-dependent manner. Prostaglandins F 70-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-107 11719525-4 2002 Serial 5"-deletion of the nur77 promoter revealed that the necessary and sufficient elements for PGF(2alpha) induction of Nur77 promoter activity are located between the nucleotides -86 and -33 upstream of the transcription start site, this region containing two AP1 elements. Prostaglandins F 97-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 26-31 11719525-4 2002 Serial 5"-deletion of the nur77 promoter revealed that the necessary and sufficient elements for PGF(2alpha) induction of Nur77 promoter activity are located between the nucleotides -86 and -33 upstream of the transcription start site, this region containing two AP1 elements. Prostaglandins F 97-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-127 11719525-6 2002 However, mutation of the AP1 sites as well as a dominant-negative JunD abolished nur77 induction by PGF(2alpha). Prostaglandins F 100-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-86 11719525-7 2002 PGF(2alpha) induces phosphorylation of JunD bound to the nur77 promoter. Prostaglandins F 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-62 11719525-10 2002 We conclude that activation of JunD through a calmodulim-dependent activation of ERK1/2 mediates nur77 induction by PGF(2alpha). Prostaglandins F 116-119 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-102 12490735-16 2002 On April 25, 2002, fulvestrant 250 mg by monthly intramuscular injection was approved by the U.S. Food and Drug Administration for the treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following antiestrogen therapy. Fulvestrant 19-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 148-164 12421108-1 2002 Anastrozole, a nonsteroidal selective aromatase inhibitor, has recently been approved in the US and several other countries for the adjuvant treatment of postmenopausal women with hormone receptor-positive early breast cancer. Anastrozole 0-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 180-196 11559707-0 2001 Silencing mediator of retinoid and thyroid hormone receptors and activating signal cointegrator-2 as transcriptional coregulators of the orphan nuclear receptor Nur77. Retinoids 22-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 161-166 11559707-5 2001 Surprisingly, histone deacetylase inhibitor trichostatin A was unable to block the repressive effect of SMRT while dramatically stimulating the Nur77 transactivation. trichostatin A 44-58 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-149 11697120-4 2001 Time-resolved resonance Raman (TR3) spectra of the radical from 4-hydroxycinnamate were measured using a probe laser wavelength of 600 nm, to be in resonance with the long wavelength absorption band of the radical. Coumaric Acids 64-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-34 11605012-2 2001 The survival benefit differs considerably between hormone receptor-positive and -negative patients, and it is believed that the effectiveness of adjuvant chemotherapy can be increased by hormonal therapy with tamoxifen. Tamoxifen 209-218 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-66 11761324-2 2001 Reduced lumiflavin was found to be bent along the N5-N10 axis, 25 degrees from planarity, which is nearly the same as previously reported restricted Hartree-Fock (RHF) calculations, which predict a bending angle of 27 degrees. lumiflavin 8-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 53-56 11761324-3 2001 The major difference in the DFT calculation is that the N10 methyl group adopts a more pseudoequatorial disposition and is only bent 13 degrees above the plane of the isoalloxazine ring system as opposed to 59 degrees in the RHF calculations. isoalloxazine 167-180 nuclear receptor subfamily 4 group A member 1 Homo sapiens 56-59 11761324-3 2001 The major difference in the DFT calculation is that the N10 methyl group adopts a more pseudoequatorial disposition and is only bent 13 degrees above the plane of the isoalloxazine ring system as opposed to 59 degrees in the RHF calculations. rhf 225-228 nuclear receptor subfamily 4 group A member 1 Homo sapiens 56-59 11761324-6 2001 This indicates that both electronic and steric interactions of the N10 methyl group of reduced lumiflavin contribute to the bent geometry. lumiflavin 95-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-70 11602619-2 2001 We found that retinoic acid inhibits the transcriptional activity of AP-1 and the orphan receptors Nur77 and Nurr1 in ACTH-secreting tumor cells. Tretinoin 14-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-104 11579340-7 2001 In those with hormone receptor-rich tumors, adjuvant chemotherapy is beneficial for HER2-positive tumors, and the regimen should contain an anthracycline. Anthracyclines 140-153 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-30 11385620-0 2001 Thapsigargin-induced apoptosis involves Cabin1-MEF2-mediated induction of Nur77. Thapsigargin 0-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-79 11385620-4 2001 The expression of Nur77 in response to TG treatment is sensitive to cyclosporin A, implicating that activation of calcineurin is necessary for Nur77 expression. Thapsigargin 39-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-23 11385620-4 2001 The expression of Nur77 in response to TG treatment is sensitive to cyclosporin A, implicating that activation of calcineurin is necessary for Nur77 expression. Thapsigargin 39-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 143-148 11385620-4 2001 The expression of Nur77 in response to TG treatment is sensitive to cyclosporin A, implicating that activation of calcineurin is necessary for Nur77 expression. Cyclosporine 68-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 18-23 11465095-3 2001 Both processes are dependent on new mRNA and protein synthesis, involve up-regulation of nur77, and can be inhibited by retinoic acids (RA). Tretinoin 136-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 11465095-8 2001 Our data suggest a complex interaction between the various isoforms of retinoid receptors in regulating T cell death and demonstrate that the target through which retinoids regulate TCR-mediated apoptosis is nur77. Retinoids 163-172 nuclear receptor subfamily 4 group A member 1 Homo sapiens 208-213 11550093-9 2001 However, inhibition of the ERK1/2 signaling pathway by PD98059 blocked the induction of Egr-1 and Nur77 mRNA while the p38 MAPK inhibitor PD169316 had little effect. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 55-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 98-103 11250200-5 2001 The structure of this 1:1 complex was determined and the hormone-receptor interface shown to be characterized by a number of hydrophilic interactions mediated by several highly ordered water networks. Water 185-190 nuclear receptor subfamily 4 group A member 1 Homo sapiens 57-73 11274386-3 2001 Because Nur77 has a putative Akt phosphorylation site at Ser-350, and phosphorylation of this residue is critical for the transactivation activity of Nur77, we investigated whether Akt regulates Nur77. Serine 57-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 8-13 11274386-5 2001 We further show that Akt specifically phosphorylates Ser-350 of the Nur77 protein within its DNA-binding domain in vitro and in vivo in 293 and NIH 3T3 cells. Serine 53-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-73 11274386-6 2001 Because phosphorylation of Ser-350 of Nur77 is critical for its function as a transcription factor, we examined the effect of Akt on this function. Serine 27-30 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 11274386-8 2001 Thus, we show that Akt interacts with Nur77 and inactivates Nur77 by phosphorylation at Ser-350 in a phosphatidylinositol 3-kinase-dependent manner, connecting the phosphatidylinositol 3-kinase-dependent Akt pathway and a nuclear receptor pathway. Serine 88-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 11274386-8 2001 Thus, we show that Akt interacts with Nur77 and inactivates Nur77 by phosphorylation at Ser-350 in a phosphatidylinositol 3-kinase-dependent manner, connecting the phosphatidylinositol 3-kinase-dependent Akt pathway and a nuclear receptor pathway. Serine 88-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-65 11134831-4 2001 A novel constant 17beta-oestradiol, intermittent norgestimate regimen has been developed based on theoretical hormone receptor dynamics in an attempt to minimise the hormonal doses needed, thereby potentially reducing the occurrence of adverse effects associated with higher oestrogen and progestogen doses. Estradiol 17-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-126 11174853-8 2001 Treatment of transfected cells with dexamethasone resulted in suppression of forskolin- or Nak1-stimulated POMC-reporter gene expression in the presence of co-transfected GR but not with GRDelta. Dexamethasone 36-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-95 11791121-4 2001 (2) Tamoxifen, administered for 5 years, significantly improves long-term survival for women of all age groups with hormone receptor-positive tumors. Tamoxifen 4-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 116-132 11205023-3 2001 This study shows that flavins, which bear electron-donating groups on the aromatic ring and/or the N-10 position, are less active and are deactivated during the course of the reaction. Flavins 22-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-103 11205023-4 2001 Moreover, flavins that are alkylated at the N-1 position instead of the N-10 position and having either no substituents or electron-withdrawing groups on the aromatic ring, remain the most active and stable. Flavins 10-17 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-76 11134831-4 2001 A novel constant 17beta-oestradiol, intermittent norgestimate regimen has been developed based on theoretical hormone receptor dynamics in an attempt to minimise the hormonal doses needed, thereby potentially reducing the occurrence of adverse effects associated with higher oestrogen and progestogen doses. norgestimate 49-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-126 11128295-12 2000 (2) The nocturnal level of salivary melatonin measured at 03:30 was 115.2 +/- 40.4 pg/mL (mean +/- SEM, N = 10) without and 51.3 +/- 18.4 pg/mL (mean +/- SEM, N = 10) with foundation garments. Melatonin 36-45 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-110 11292179-6 2000 Increasing intracellular Ca2+ concentration ([Ca2+]i) by thapsgargin and A23187 induced the expression of both c-fos and nur77 mRNA expression, and synergistic effects were observed when cells were incubated with sodium butyrate plus thapsgargin and A23187. thapsgargin 57-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-126 11292179-6 2000 Increasing intracellular Ca2+ concentration ([Ca2+]i) by thapsgargin and A23187 induced the expression of both c-fos and nur77 mRNA expression, and synergistic effects were observed when cells were incubated with sodium butyrate plus thapsgargin and A23187. Calcimycin 73-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-126 11292179-6 2000 Increasing intracellular Ca2+ concentration ([Ca2+]i) by thapsgargin and A23187 induced the expression of both c-fos and nur77 mRNA expression, and synergistic effects were observed when cells were incubated with sodium butyrate plus thapsgargin and A23187. Butyric Acid 213-228 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-126 11292179-6 2000 Increasing intracellular Ca2+ concentration ([Ca2+]i) by thapsgargin and A23187 induced the expression of both c-fos and nur77 mRNA expression, and synergistic effects were observed when cells were incubated with sodium butyrate plus thapsgargin and A23187. thapsgargin 234-245 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-126 11292179-6 2000 Increasing intracellular Ca2+ concentration ([Ca2+]i) by thapsgargin and A23187 induced the expression of both c-fos and nur77 mRNA expression, and synergistic effects were observed when cells were incubated with sodium butyrate plus thapsgargin and A23187. Calcimycin 250-256 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-126 11292179-8 2000 These results suggest that although sodium butyrate altered Ca2+ signaling which is an important regulatory mechanism for c-fos and nur77 expression, nevertheless the sodium butyrate-induced c-fos and nur77 expression may be not in fact mediated through Ca2+ signaling. Butyric Acid 36-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-137 11292179-8 2000 These results suggest that although sodium butyrate altered Ca2+ signaling which is an important regulatory mechanism for c-fos and nur77 expression, nevertheless the sodium butyrate-induced c-fos and nur77 expression may be not in fact mediated through Ca2+ signaling. Butyric Acid 167-182 nuclear receptor subfamily 4 group A member 1 Homo sapiens 201-206 11292179-0 2000 Alterations in Ca2+ signaling, and c-fos and nur77 expression are associated with sodium butyrate-induced differentiation of C6 glioma cell. Butyric Acid 82-97 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-50 11292179-5 2000 Sodium butyrate per se enhanced the expression of c-fos mRNA, and the enhanced levels were maintained for 24 h, but over the same time period, the initially increased levels of nur77 expression tailed off, while c-myc expression was slightly reduced. Butyric Acid 0-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 177-182 12057165-10 2000 Adjuvant hormonal therapy with tamoxifen improves DFS and OS in patients with hormone receptor (HR)-positive tumors, and ovarian ablation should be considered in premenopausal patients with HR-positive tumors and multiple involved nodes or stage IIIB disease. Tamoxifen 31-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 78-94 10944115-1 2000 T-cell antigen receptor (TCR)-induced thymocyte apoptosis is mediated by calcium-dependent signal transduction pathways leading to the transcriptional activation of members of the Nur77 family. Calcium 73-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 180-185 10944115-2 2000 The major calcium- and calcineurin-responsive elements in the Nur77 promoter are binding sites for myocyte enhancer factor-2 (MEF2). Calcium 10-17 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 12057165-10 2000 Adjuvant hormonal therapy with tamoxifen improves DFS and OS in patients with hormone receptor (HR)-positive tumors, and ovarian ablation should be considered in premenopausal patients with HR-positive tumors and multiple involved nodes or stage IIIB disease. Tamoxifen 31-40 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-98 10933397-2 2000 MEF2 has been shown to be the major transcription factor responsible for calcium-dependent Nur77 transcription. Calcium 73-80 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-96 10945021-2 2000 Recent development in the field of adjuvant chemo/endocrine therapy is an usage of LH-RH analogue with tamoxifen for premenopausal hormone receptor positive women, and also an emerging role of taxans. Tamoxifen 103-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 131-147 10919358-0 2000 Transcriptional induction of Nur77 by indomethacin that results in apoptosis of colon cancer cells. Indomethacin 38-50 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-34 10919358-2 2000 Here, we report that indomethacin induced the expression of Nur77 which has been implicated in activation-induced apoptosis of T-lymphocytes, in a colon cancer cell line, HCT-15. Indomethacin 21-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-65 10919358-3 2000 The transcript- and protein-level, the transcriptional activity of Nur77 promoter, and the DNA binding of Nur77 were significantly induced following indomethacin treatment. Indomethacin 149-161 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-72 10919358-3 2000 The transcript- and protein-level, the transcriptional activity of Nur77 promoter, and the DNA binding of Nur77 were significantly induced following indomethacin treatment. Indomethacin 149-161 nuclear receptor subfamily 4 group A member 1 Homo sapiens 106-111 10933397-7 2000 Thus, activation of MEF2 and the consequent transcription of Nur77 are controlled by the association of MEF2 with the histone deacetylases via the calcium-dependent repressor Cabin1. Calcium 147-154 nuclear receptor subfamily 4 group A member 1 Homo sapiens 61-66 10773199-0 2000 Differential patterns of induction of NGFI-B, Nor1 and c-fos mRNAs in striatal subregions by haloperidol and clozapine. Haloperidol 93-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-44 10772826-0 2000 Retinoic acid and its receptors repress the expression and transactivation functions of Nur77: a possible mechanism for the inhibition of apoptosis by retinoic acid. Tretinoin 0-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-93 10772826-0 2000 Retinoic acid and its receptors repress the expression and transactivation functions of Nur77: a possible mechanism for the inhibition of apoptosis by retinoic acid. Tretinoin 151-164 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-93 10772826-3 2000 To illustrate the mechanism of the inhibition, we examined the effects of retinoic acid (RA) on the expression and transactivation functions of Nur77 in the human peripheral blood mononuclear cells and the human T-cell leukemia, Jurkat. Tretinoin 74-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-149 10772826-3 2000 To illustrate the mechanism of the inhibition, we examined the effects of retinoic acid (RA) on the expression and transactivation functions of Nur77 in the human peripheral blood mononuclear cells and the human T-cell leukemia, Jurkat. Tretinoin 89-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 144-149 10772826-8 2000 Taken all together, we demonstrated that RA repressed Nur77 function through multiple mechanisms that may provide the basis for RA inhibition on the apoptosis of activated T-lymphocytes. Tretinoin 41-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-59 10772826-8 2000 Taken all together, we demonstrated that RA repressed Nur77 function through multiple mechanisms that may provide the basis for RA inhibition on the apoptosis of activated T-lymphocytes. Tretinoin 128-130 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-59 10773199-2 2000 In this study we have compared the regulation of mRNAs for the nuclear orphan receptor NGFI-B, which forms a functional heterodimer with the retinoid x receptor and the related orphan nuclear receptor Nor1 with c-fos mRNA after acute and chronic treatments with haloperidol and clozapine. Clozapine 278-287 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-93 10773199-5 2000 Acute haloperidol treatment increased NGFI-B, Nor1 and c-fos mRNAs in nucleus accumbens shell and core as well as medial and lateral caudate putamen. Haloperidol 6-17 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-44 10939640-0 2000 Etoposide stimulates 1,25-dihydroxyvitamin D3 differentiation activity, hormone binding and hormone receptor expression in HL-60 human promyelocytic cells. Etoposide 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-108 10773199-0 2000 Differential patterns of induction of NGFI-B, Nor1 and c-fos mRNAs in striatal subregions by haloperidol and clozapine. Clozapine 109-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-44 10773199-6 2000 In contrast, clozapine lead to an increase of NGFI-B, Nor1 and c-fos only in the accumbens shell. Clozapine 13-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-52 10773199-2 2000 In this study we have compared the regulation of mRNAs for the nuclear orphan receptor NGFI-B, which forms a functional heterodimer with the retinoid x receptor and the related orphan nuclear receptor Nor1 with c-fos mRNA after acute and chronic treatments with haloperidol and clozapine. Haloperidol 262-273 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-93 10773199-8 2000 Chronic haloperidol lead to an increase of NGFI-B mRNA in the accumbens core. Haloperidol 8-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-49 11556039-7 2000 However, the response elicited in a case of the ER-/PR- phenotype justified the randomized use of tamoxifen among patients in Iraq where the necessary requirements for hormone receptor assessment are almost unavailable. Tamoxifen 98-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 168-184 10773199-10 2000 Also, the increased levels of NGFI-B, which is an important component in retinoid signaling, both after acute and chronic treatments of haloperidol suggests altered sensitivity to retinoids which could be an important component for the beneficial antipsychotic effect. Retinoids 73-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-36 10773199-10 2000 Also, the increased levels of NGFI-B, which is an important component in retinoid signaling, both after acute and chronic treatments of haloperidol suggests altered sensitivity to retinoids which could be an important component for the beneficial antipsychotic effect. Haloperidol 136-147 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-36 10773199-10 2000 Also, the increased levels of NGFI-B, which is an important component in retinoid signaling, both after acute and chronic treatments of haloperidol suggests altered sensitivity to retinoids which could be an important component for the beneficial antipsychotic effect. Retinoids 180-189 nuclear receptor subfamily 4 group A member 1 Homo sapiens 30-36 10745271-0 2000 Ceramide-induced cell death is independent of the Fas/Fas ligand pathway and is prevented by Nur77 overexpression in A20 B cells. Ceramides 0-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 93-98 10745271-6 2000 We also found that overexpression of Nur77, a zinc-finger transcription factor described to upregulate FasL, antagonizes ceramide-induced apoptosis, but not Fas-induced apoptosis. Ceramides 121-129 nuclear receptor subfamily 4 group A member 1 Homo sapiens 37-42 10745271-8 2000 Ceramide-induced cell death was associated with increased c-myc, p53, Bax and p27kip1 levels; in contrast, cells transfected with Nur77 (A20Nur77), resistant to ceramide-induced apoptosis, showed a marked downregulation of p53 after ceramide treatment, with neither Bax nor p27kip1 induction. Ceramides 161-169 nuclear receptor subfamily 4 group A member 1 Homo sapiens 130-135 10745271-8 2000 Ceramide-induced cell death was associated with increased c-myc, p53, Bax and p27kip1 levels; in contrast, cells transfected with Nur77 (A20Nur77), resistant to ceramide-induced apoptosis, showed a marked downregulation of p53 after ceramide treatment, with neither Bax nor p27kip1 induction. Ceramides 233-241 nuclear receptor subfamily 4 group A member 1 Homo sapiens 130-135 10745271-9 2000 In conclusion, our results suggest that, in the A20 B cell line, Fas and ceramide trigger two distinct pathways and that Nur77 overexpression confers protection against ceramide-mediated apoptosis which correlates with inhibition of p53, Bax and p27kip1 induction. Ceramides 169-177 nuclear receptor subfamily 4 group A member 1 Homo sapiens 121-126 9987007-1 1999 In the present study in situ hybridization was used to study the effect of kainic acid induced seizures on the expression of the zinc finger immediate-early genes (IEGs) NGFI-A, NGFI-B, NGFI-C, egr-2; egr-3 and Nurr1. Kainic Acid 75-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 178-184 10531067-1 1999 T cell receptor (TCR)-induced apoptosis of thymocytes is mediated by calcium-dependent expression of the steroid receptors Nur77 and Nor1. Calcium 69-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 123-128 10895028-0 2000 Endometrial response to sexual steroids as assessed by prostaglandin F(2alpha) output in explant culture and hormone receptor expression. Steroids 31-39 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-125 9818284-0 1998 Association between [18F]fluorodeoxyglucose uptake and postoperative histopathology, hormone receptor status, thymidine labelling index and p53 in primary breast cancer: a preliminary observation. Fluorodeoxyglucose F18 20-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 9885901-6 1998 Both the transgenic Bcl-2 and zVAD-fmk, an inhibitor of caspases, affected all features of Dex-induced apoptosis in a similar fashion, by inhibiting cell death and PARP cleavage, and by stabilizing AP-1, NF-kappaB p50-p50 and NUR-77 levels. benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone 30-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 226-232 9885901-6 1998 Both the transgenic Bcl-2 and zVAD-fmk, an inhibitor of caspases, affected all features of Dex-induced apoptosis in a similar fashion, by inhibiting cell death and PARP cleavage, and by stabilizing AP-1, NF-kappaB p50-p50 and NUR-77 levels. Dexamethasone 91-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 226-232 9885901-4 1998 Dex-induced apoptotic commitment was preceded by the rapid (3 h) cleavage of both a typical caspase substrate, poly(ADP-ribose) polymerase (PARP), and of nuclear transcription factors AP-1, NF-kappaB p50-p50 and NUR-77. Dexamethasone 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 212-218 9885901-5 1998 By contrast, phorbol myristate acetate (PMA) and/or ionomycin-induced apoptosis had much slower kinetics, were preceded by an early increase of NF-kappaB/RelA-p50, AP-1 and NUR-77 activities, and were insensitive to proteasome inhibition. Tetradecanoylphorbol Acetate 13-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 173-179 9885901-5 1998 By contrast, phorbol myristate acetate (PMA) and/or ionomycin-induced apoptosis had much slower kinetics, were preceded by an early increase of NF-kappaB/RelA-p50, AP-1 and NUR-77 activities, and were insensitive to proteasome inhibition. Tetradecanoylphorbol Acetate 40-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 173-179 9885901-5 1998 By contrast, phorbol myristate acetate (PMA) and/or ionomycin-induced apoptosis had much slower kinetics, were preceded by an early increase of NF-kappaB/RelA-p50, AP-1 and NUR-77 activities, and were insensitive to proteasome inhibition. Ionomycin 52-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 173-179 9564841-0 1998 Antisense TR3 orphan receptor can increase prostate cancer cell viability with etoposide treatment. Etoposide 79-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-29 9747867-0 1998 erbB-2 and response to doxorubicin in patients with axillary lymph node-positive, hormone receptor-negative breast cancer. Doxorubicin 23-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-98 9564841-4 1998 Northern blot analysis shows that human TR3 orphan receptor expression can be induced rapidly after treatment of LNCaP and PC-3 prostate cancer cells with calcium ionophore or etoposide. Calcium 155-162 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-59 9564841-4 1998 Northern blot analysis shows that human TR3 orphan receptor expression can be induced rapidly after treatment of LNCaP and PC-3 prostate cancer cells with calcium ionophore or etoposide. Etoposide 176-185 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-59 9564841-5 1998 Our data further demonstrate that a much higher concentration of etoposide was needed to kill the same number of cells in LNCaP and PC-3 cells transfected stably with antisense TR3 orphan receptor compared with that in control vector transfectants. Etoposide 65-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 177-196 9341769-6 1997 The expression of c-myc and nur77, two immediate-early genes implicated in FasL gene activation, was blocked by lactacystin. lactacystin 112-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 9353409-11 1997 These benzophenone-containing CT analogs should facilitate studies of hormone-receptor interactions and allow the direct identification of a CT binding domain(s) within the receptor by the analysis of photochemically cross-linked conjugates. benzophenone 6-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-86 9439682-4 1997 In addition, N10 had a 1.65-fold higher GSH level than did KB and became radiosensitive on treatment with buthionine sulfoximine, an inhibitor of GSH. Glutathione 40-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-16 9439682-4 1997 In addition, N10 had a 1.65-fold higher GSH level than did KB and became radiosensitive on treatment with buthionine sulfoximine, an inhibitor of GSH. Buthionine Sulfoximine 106-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-16 9439682-4 1997 In addition, N10 had a 1.65-fold higher GSH level than did KB and became radiosensitive on treatment with buthionine sulfoximine, an inhibitor of GSH. Glutathione 146-149 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-16 9439682-8 1997 X-Irradiation caused a rapid induction of PARP activity within 1 h in both cell lines, but treatment of cells with nicotinamide, a PARP inhibitor, markedly reduced the enzyme induction in N10, but not in KB, and potentiated the radiosensitivity in N10. Niacinamide 115-127 nuclear receptor subfamily 4 group A member 1 Homo sapiens 188-191 9439682-8 1997 X-Irradiation caused a rapid induction of PARP activity within 1 h in both cell lines, but treatment of cells with nicotinamide, a PARP inhibitor, markedly reduced the enzyme induction in N10, but not in KB, and potentiated the radiosensitivity in N10. Niacinamide 115-127 nuclear receptor subfamily 4 group A member 1 Homo sapiens 248-251 9322922-6 1997 Substitutions of Ser354 with negatively charged amino acids, such as Asp or Glu, dramatically decreased Nur77 DNA-binding and trans-activation activities, whereas mutation to the neutral Ala had no effect. Aspartic Acid 69-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-109 9322922-6 1997 Substitutions of Ser354 with negatively charged amino acids, such as Asp or Glu, dramatically decreased Nur77 DNA-binding and trans-activation activities, whereas mutation to the neutral Ala had no effect. Glutamic Acid 76-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 104-109 9130711-0 1997 Modulation of retinoic acid sensitivity in lung cancer cells through dynamic balance of orphan receptors nur77 and COUP-TF and their heterodimerization. Tretinoin 14-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-110 9130711-4 1997 Here, we present evidence that nur77, another orphan receptor whose expression is highly induced by phorbol esters and growth factors, is involved in modulation of the RA response. Phorbol Esters 100-114 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-36 9130711-5 1997 Expression of nur77 enhances ligand-independent transactivation of RA response elements (RAREs) and desensitizes their RA responsiveness. Tretinoin 67-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-19 9130711-12 1997 These observations demonstrate that a dynamic equilibrium between orphan receptors nur77 and COUP-TF, through their heterodimerization that regulates COUP-TF RARE binding, is critical for RA responsiveness of human lung cancer cells. Tretinoin 158-160 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-88 11243104-4 1997 Of the 308 cases, tumor specimens in 130 patients were subjected to hormone receptor analysis by a dextran-coated charcoal technique. Dextrans 99-106 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-84 8943276-10 1996 Trp-104 in the receptor, a key residue in the hormone-receptor interaction, has an altered conformation in the low affinity site enabling a favorable hydrogen bond to be formed with Asp-116 of the hormone. Tryptophan 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-62 9070291-5 1997 In the presence of cycloheximide, all-trans retinoic acid superinduced NOR-1 mRNA, whereas all-trans and 9-cis retinoic acids strongly suppressed the NGFI-B mRNA accumulation. Tretinoin 111-125 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-156 8943276-10 1996 Trp-104 in the receptor, a key residue in the hormone-receptor interaction, has an altered conformation in the low affinity site enabling a favorable hydrogen bond to be formed with Asp-116 of the hormone. Hydrogen 150-158 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-62 8943276-10 1996 Trp-104 in the receptor, a key residue in the hormone-receptor interaction, has an altered conformation in the low affinity site enabling a favorable hydrogen bond to be formed with Asp-116 of the hormone. Aspartic Acid 182-185 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-62 8621434-5 1996 Both TrkC and TrkA mediate qualitatively similar increases in the tyrosine phosphorylation of phospholipase C (PLC)-gamma1, Shc, SNT, and MAPK and the transcription of the c-fos, c-jun, NGFI-A, and NGFI-B immediate early genes. Tyrosine 66-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 198-204 11666896-6 1996 The D(2)(d)() symmetric bispentazole (21) is the lowest energy N(10) minimum but is 260 kcal/mol higher in energy than five N(2) molecules. ispentazole 25-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-69 8702665-5 1996 Hormone receptor-dependent stimulation of cAMP accumulation in cells expressing alphas-R231H is reduced by approximately 75% in comparison to cAMP accumulation in cells expressing alphas-WT. Cyclic AMP 42-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 8702665-5 1996 Hormone receptor-dependent stimulation of cAMP accumulation in cells expressing alphas-R231H is reduced by approximately 75% in comparison to cAMP accumulation in cells expressing alphas-WT. Cyclic AMP 142-146 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 8702665-8 1996 In three-dimensional structures of G protein heterotrimers, Arg-231 is located in a region, switch 2, that is thought to interact with the betagamma subunit rather than with the hormone receptor. Arginine 60-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 178-194 8640701-3 1996 Additional chemotherapy and tamoxifen, in hormone receptor-positive tumors, was used after mastectomy. Tamoxifen 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 42-58 8883941-0 1996 Cellular expression of the immediate early transcription factors Nurr1 and NGFI-B suggests a gene regulatory role in several brain regions including the nigrostriatal dopamine system. Dopamine 167-175 nuclear receptor subfamily 4 group A member 1 Homo sapiens 75-81 8883941-1 1996 Nurr1 and NGFI-B are closely related orphan members of the steroid-thyroid hormone receptor family involved in immediate early responses to stimuli such as growth factors. Steroids 59-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 10-16 8647183-4 1996 Furthermore, studies with thymocytes demonstrated that the induction of nur77, a gene shown to be involved in thymocyte apoptosis signaled through the TCR or its surrogates, is not inhibited by NAC or dependent upon molecular oxygen. Oxygen 226-232 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-77 7499374-0 1995 Chemical modification of the N-10 ribityl side chain of flavins. Flavins 56-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-33 8613792-5 1996 After ether exposure, c-fos and NGFI-B mRNA induction were maximal at 30--60 min, whereas Fos protein peaked at 60--120 min. Ether 6-11 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-38 7499374-2 1995 Three flavin derivatives modified at the 2"-position of the flavin N-10 ribityl side chain were synthesized: arabinoflavin, 2"-F-2"-deoxyarabinoflavin, and 2"-deoxyriboflavin. 4,6-dinitro-o-cresol 6-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-71 7499374-2 1995 Three flavin derivatives modified at the 2"-position of the flavin N-10 ribityl side chain were synthesized: arabinoflavin, 2"-F-2"-deoxyarabinoflavin, and 2"-deoxyriboflavin. 4,6-dinitro-o-cresol 60-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 67-71 7579652-3 1995 Some encouraging results have been obtained using designed metal-binding sites in such diverse applications as the stabilization of artificial peptide assembly, regulation of membrane channels, control of enzyme activity and enhancement of hormone-receptor interactions. Metals 59-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 240-256 7565789-4 1995 We show that the major control of Nur77 induction is mediated by the calcium signaling pathway. Calcium 69-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-39 7565789-7 1995 CsA decreases both Nur77 protein levels and promoter activity, and the kinetics of CsA inhibition of apoptosis correlates with a decrease in Nur77 protein levels. Cyclosporine 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-24 7565789-7 1995 CsA decreases both Nur77 protein levels and promoter activity, and the kinetics of CsA inhibition of apoptosis correlates with a decrease in Nur77 protein levels. Cyclosporine 83-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 141-146 7565789-9 1995 In addition, Nur77 promoter deletion analysis revealed two RSRF (related to serum-responsive factor) binding sites, which can confer calcium and CsA sensitivity on a heterologous promoter. Calcium 133-140 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 7565789-9 1995 In addition, Nur77 promoter deletion analysis revealed two RSRF (related to serum-responsive factor) binding sites, which can confer calcium and CsA sensitivity on a heterologous promoter. Cyclosporine 145-148 nuclear receptor subfamily 4 group A member 1 Homo sapiens 13-18 7565789-10 1995 Taken together, our data suggest that the levels of transcriptional induction of Nur77 play an important role during activation-induced apoptosis and that calcium signals regulate a novel CsA-sensitive nuclear factor required for Nur77 transcription in T cells. Calcium 155-162 nuclear receptor subfamily 4 group A member 1 Homo sapiens 230-235 8544841-5 1995 The normal response to cAMP could probably be attributed to equal activation of both genes by a transcription factor Nur77. Cyclic AMP 23-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 117-122 7705655-0 1995 A novel pathway for vitamin A signaling mediated by RXR heterodimerization with NGFI-B and NURR1. Vitamin A 20-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-86 7705655-7 1995 Because expression of both NGFI-B and NURR1 is rapidly induced by various growth factors, these findings also suggest a novel mechanism for convergence between vitamin A or retinoid and growth factor signaling pathways. Vitamin A 160-169 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-33 7705655-7 1995 Because expression of both NGFI-B and NURR1 is rapidly induced by various growth factors, these findings also suggest a novel mechanism for convergence between vitamin A or retinoid and growth factor signaling pathways. Retinoids 173-181 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-33 7579504-1 1995 In pre-clinical and limited clinical studies, high doses ( > or = 200 mg/day) of the triphenylethylene derivative toremifene showed activity in estrogen receptor (ER) negative and ER-unknown metastatic breast cancer after progression on tamoxifen, and a mechanism of action independent of hormone receptor binding was speculated. triphenylethylene 88-105 nuclear receptor subfamily 4 group A member 1 Homo sapiens 292-308 7831306-6 1995 We report here that CsA inhibits the TCR-mediated activation of Nur77 protein in T-cell hybridomas by blocking the DNA binding activity of Nur77 protein rather than its de novo synthesis. Cyclosporine 20-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-69 7831306-6 1995 We report here that CsA inhibits the TCR-mediated activation of Nur77 protein in T-cell hybridomas by blocking the DNA binding activity of Nur77 protein rather than its de novo synthesis. Cyclosporine 20-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 7831306-7 1995 We also show that CsA mediates its negative effects on the Nur77 DNA binding activity through the N-terminal region of the protein. Cyclosporine 18-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-64 7831306-8 1995 This complete inhibition of Nur77 protein DNA binding activity may explain how CsA interferes with TCR-mediated apoptosis. Cyclosporine 79-82 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 7579504-1 1995 In pre-clinical and limited clinical studies, high doses ( > or = 200 mg/day) of the triphenylethylene derivative toremifene showed activity in estrogen receptor (ER) negative and ER-unknown metastatic breast cancer after progression on tamoxifen, and a mechanism of action independent of hormone receptor binding was speculated. Toremifene 117-127 nuclear receptor subfamily 4 group A member 1 Homo sapiens 292-308 7579504-2 1995 The CALGB conducted a Phase II trial (CALGB 8945) to test the efficacy of high dose toremifene in a population of patients who had hormone receptor-negative, metastatic breast cancer with limited prior chemotherapy exposure, good performance status, and measurable disease. Toremifene 84-94 nuclear receptor subfamily 4 group A member 1 Homo sapiens 131-147 7930567-8 1994 Con A-induced activation of NGFI-B gene expression was not overcome by cyclosporin A or by 8Br-cAMP, but was partially prevented by dexamethasone. Dexamethasone 132-145 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-34 7981602-5 1994 Various inhibitors of TCR-mediated apoptosis, including cyclosporin A down-regulate the Nur77 DNA binding activity. Cyclosporine 56-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-93 7930567-9 1994 In lymphoblasts, okadaic acid caused the induction of NGFI-B gene expression, indicating a role for the serine/threonine protein phosphatases PP1 and PP2A in the regulation of this gene in resting cells. Okadaic Acid 17-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-60 7930567-3 1994 After stimulation of T lymphocytes with Con A or phorbol 12,13 dibutyrate (PDBu), NGFI-B gene expression showed an induction of at least sevenfold within 3 h of stimulation. Phorbol 12,13-Dibutyrate 49-73 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-88 7930567-3 1994 After stimulation of T lymphocytes with Con A or phorbol 12,13 dibutyrate (PDBu), NGFI-B gene expression showed an induction of at least sevenfold within 3 h of stimulation. Phorbol 12,13-Dibutyrate 75-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-88 7930567-7 1994 However, the induction of NGFI-B by IL-2 is dependent on the presence of cycloheximide. Cycloheximide 73-86 nuclear receptor subfamily 4 group A member 1 Homo sapiens 26-32 7930567-8 1994 Con A-induced activation of NGFI-B gene expression was not overcome by cyclosporin A or by 8Br-cAMP, but was partially prevented by dexamethasone. Cyclosporine 71-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-34 7930567-10 1994 Okadaic acid-induced NGFI-B transcripts were significantly more stable than PDBu-induced NGFI-B mRNA. Okadaic Acid 0-12 nuclear receptor subfamily 4 group A member 1 Homo sapiens 21-27 8405432-0 1993 Solvent oxygen is not incorporated into N10-formyltetrahydrofolate in the reaction catalyzed by N10-formyltetrahydrofolate synthetase. Oxygen 8-14 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-99 7706656-5 1994 Positive hormone receptor assays on the surgical specimen favoured ovarian steroid hormone involvement in the aetiopathology of this strange disease. Steroids 75-90 nuclear receptor subfamily 4 group A member 1 Homo sapiens 9-25 8405432-1 1993 The mechanism of the reaction catalyzed by N10-formyltetrahydrofolate synthetase involves the formation of formyl phosphate as an intermediate which then formylates tetrahydrofolate at the N-10 position. formyl phosphate 107-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-46 8405432-1 1993 The mechanism of the reaction catalyzed by N10-formyltetrahydrofolate synthetase involves the formation of formyl phosphate as an intermediate which then formylates tetrahydrofolate at the N-10 position. formyl phosphate 107-123 nuclear receptor subfamily 4 group A member 1 Homo sapiens 189-193 8405432-1 1993 The mechanism of the reaction catalyzed by N10-formyltetrahydrofolate synthetase involves the formation of formyl phosphate as an intermediate which then formylates tetrahydrofolate at the N-10 position. formylates tetrahydrofolate 154-181 nuclear receptor subfamily 4 group A member 1 Homo sapiens 43-46 8405432-1 1993 The mechanism of the reaction catalyzed by N10-formyltetrahydrofolate synthetase involves the formation of formyl phosphate as an intermediate which then formylates tetrahydrofolate at the N-10 position. formylates tetrahydrofolate 154-181 nuclear receptor subfamily 4 group A member 1 Homo sapiens 189-193 8405432-4 1993 If this were the case, oxygen from solvent H2O would be incorporated into the formyl group of the N10-derivative. Oxygen 23-29 nuclear receptor subfamily 4 group A member 1 Homo sapiens 98-101 8405432-4 1993 If this were the case, oxygen from solvent H2O would be incorporated into the formyl group of the N10-derivative. Water 43-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 98-101 8405432-5 1993 By conducting the reaction in a 1:1 mixture of [16O]H2O and [18O]H2O and using 13C NMR spectroscopy we show that no 18O is incorporated into the product and conclude that the reaction proceeds via a direct formylation of the N-10 position by formyl phosphate. formyl phosphate 242-258 nuclear receptor subfamily 4 group A member 1 Homo sapiens 225-229 8395013-5 1993 The key features that distinguished the NGFI-B and SF-1 interactions were an amino group in the minor groove of the SF-1 binding sequence and an asparagine in the SF-1 A box. Asparagine 145-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-46 1419299-5 1992 In this series of relapsing patients, [3H]dT LI was unrelated to hormone receptor status in the primary tumour, but it was higher in the metachronous lesions from patients with hormone receptor-negative primary tumours. Tritium 39-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 177-193 1323288-0 1992 ABA-induced "lipid melting" and its reversal by umbelliferone in the plasmalemma of guard cell protoplasts: a breakthrough in plant hormone-receptor binding and hormone action. alisol B 23-acetate 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-148 1323288-0 1992 ABA-induced "lipid melting" and its reversal by umbelliferone in the plasmalemma of guard cell protoplasts: a breakthrough in plant hormone-receptor binding and hormone action. 7-hydroxycoumarin 48-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 132-148 1326675-3 1992 The treatment with the ACE inhibitor captopril led to activation of hormone-receptor interactions. Captopril 37-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-84 8247024-7 1993 To ascertain that this phenomenon was not unique to insect cells, aldosterone induced MR nuclear translocation in mouse macrophage cells was also demonstrated immunocytochemically, clearly indicating a role for nuclear translocation in MR function. Aldosterone 66-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-88 8247024-7 1993 To ascertain that this phenomenon was not unique to insect cells, aldosterone induced MR nuclear translocation in mouse macrophage cells was also demonstrated immunocytochemically, clearly indicating a role for nuclear translocation in MR function. Aldosterone 66-77 nuclear receptor subfamily 4 group A member 1 Homo sapiens 236-238 8095544-1 1993 Chlorpromazine N-oxide, fluphenazine N4"-oxide, prochlorperazine N4"-oxide, sulforidazine N-oxide, and trifluoperazine N4"-oxide were synthesized by oxidation of the designated nitrogen atom in the N-10 side chain of the respective parent drug with 3-chloroperoxybenzoic acid. trifluoperazine N(4')-oxide 103-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 198-202 8095544-1 1993 Chlorpromazine N-oxide, fluphenazine N4"-oxide, prochlorperazine N4"-oxide, sulforidazine N-oxide, and trifluoperazine N4"-oxide were synthesized by oxidation of the designated nitrogen atom in the N-10 side chain of the respective parent drug with 3-chloroperoxybenzoic acid. Nitrogen 177-185 nuclear receptor subfamily 4 group A member 1 Homo sapiens 198-202 1644831-3 1992 However, the ligand for NGFI-B does not appear to be a component of cell culture medium, as NGFI-B remained active when expressed in cells grown in medium lacking phenol red, serum, essential vitamins, or essential amino acids. Phenolsulfonphthalein 163-173 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-98 1644831-3 1992 However, the ligand for NGFI-B does not appear to be a component of cell culture medium, as NGFI-B remained active when expressed in cells grown in medium lacking phenol red, serum, essential vitamins, or essential amino acids. essential vitamins 182-200 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-98 1644831-3 1992 However, the ligand for NGFI-B does not appear to be a component of cell culture medium, as NGFI-B remained active when expressed in cells grown in medium lacking phenol red, serum, essential vitamins, or essential amino acids. Amino Acids, Essential 205-226 nuclear receptor subfamily 4 group A member 1 Homo sapiens 92-98 1644831-5 1992 The mutation of two adjacent serine and threonine residues within TAB-1 significantly decreased transactivation by NGFI-B. Serine 29-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-121 1644831-5 1992 The mutation of two adjacent serine and threonine residues within TAB-1 significantly decreased transactivation by NGFI-B. Threonine 40-49 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-121 1314418-3 1992 A domain separate from the NGFI-B zinc fingers, termed the A box, was identified and is required for recognition of the two adenine-thymidine (A-T) base pairs at the 5" end of the NGFI-B DNA binding element. adenine-thymidine 124-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-33 1314418-3 1992 A domain separate from the NGFI-B zinc fingers, termed the A box, was identified and is required for recognition of the two adenine-thymidine (A-T) base pairs at the 5" end of the NGFI-B DNA binding element. adenine-thymidine 124-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 180-186 1558805-7 1992 A negative association emerged which was also observed in vitro in the human breast cancer line MCF-7 treated with Sodium Butyrate, a differentiation inducer, which reduced hormone-receptor levels and increased CaMBr8 expression. Butyric Acid 115-130 nuclear receptor subfamily 4 group A member 1 Homo sapiens 173-189 1651101-0 1991 Phorbol ester, forskolin, and serum induction of a human colon nuclear hormone receptor gene related to the NUR 77/NGFI-B genes. Phorbol Esters 0-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-114 1655735-2 1991 The overproduced hMR binds aldosterone with high affinity (Kd = 1.36 nM) and has high affinity for cortisol, cortexolone, and progesterone. Aldosterone 27-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-20 1655735-2 1991 The overproduced hMR binds aldosterone with high affinity (Kd = 1.36 nM) and has high affinity for cortisol, cortexolone, and progesterone. Hydrocortisone 99-107 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-20 1655735-2 1991 The overproduced hMR binds aldosterone with high affinity (Kd = 1.36 nM) and has high affinity for cortisol, cortexolone, and progesterone. Cortodoxone 109-120 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-20 1655735-2 1991 The overproduced hMR binds aldosterone with high affinity (Kd = 1.36 nM) and has high affinity for cortisol, cortexolone, and progesterone. Progesterone 126-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 17-20 1655735-10 1991 Unlike the glucocorticoid receptor, the oligomeric hMR complex can bind DNA-cellulose without prior activation. Cellulose 76-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-54 1895294-5 1991 The bridge-extended analogues isohomo-PDDF (7) and isohomo-DMPDDF (8) contain an additional methylene group interposed between N10 and the phenyl ring of 1 and 3, respectively. isohomo-pddf 30-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 127-130 1895294-5 1991 The bridge-extended analogues isohomo-PDDF (7) and isohomo-DMPDDF (8) contain an additional methylene group interposed between N10 and the phenyl ring of 1 and 3, respectively. isohomo-dmpddf 51-65 nuclear receptor subfamily 4 group A member 1 Homo sapiens 127-130 1651101-0 1991 Phorbol ester, forskolin, and serum induction of a human colon nuclear hormone receptor gene related to the NUR 77/NGFI-B genes. Phorbol Esters 0-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-121 1651101-0 1991 Phorbol ester, forskolin, and serum induction of a human colon nuclear hormone receptor gene related to the NUR 77/NGFI-B genes. Colforsin 15-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-114 1651101-0 1991 Phorbol ester, forskolin, and serum induction of a human colon nuclear hormone receptor gene related to the NUR 77/NGFI-B genes. Colforsin 15-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 115-121 1651101-5 1991 ST-59 receptor induction by serum was greatly amplified by cycloheximide and could be detected in actively growing LS-180 cells. Cycloheximide 59-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 2283997-7 1990 The mRNA of NAK1 was induced rapidly and transiently by growth-stimulating agents, such as adenosine diphosphate, in monkey kidney cells (BSC-1), by phytohemagglutinin in human lymphocytes, and by serum stimulation of arrested fibroblasts. Adenosine Diphosphate 91-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 12-16 1809075-4 1991 The standardized DCC method is the most common and recognized (Food and Drug Administration) procedure for quantifying hormone receptor in human cancer. DICYCLOHEXYLCARBODIIMIDE 17-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-135 1874033-6 1991 However, since modification of either the hormone or the carbohydrate moiety of the receptor can selectively attenuate either the insulin-like or the lipolytic response, more than one hormone receptor interaction is likely. Carbohydrates 57-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 184-200 33760860-1 2021 Letrozole, an aromatase inhibitor (AI), is the first-line adjuvant drug for treating hormone receptor-positive (HR+) breast cancer in postmenopausal women. Letrozole 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 2358463-7 1990 The down-regulation of the hormone receptor was also induced with another phorbol diester, phorbol 12,13-didecanoate, but not with the phorbol or phorbol monoesters phorbol 12-myristate and phorbol 13-acetate. Phorbol Esters 74-89 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-43 2358463-7 1990 The down-regulation of the hormone receptor was also induced with another phorbol diester, phorbol 12,13-didecanoate, but not with the phorbol or phorbol monoesters phorbol 12-myristate and phorbol 13-acetate. phorbol-12,13-didecanoate 91-116 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-43 2358463-7 1990 The down-regulation of the hormone receptor was also induced with another phorbol diester, phorbol 12,13-didecanoate, but not with the phorbol or phorbol monoesters phorbol 12-myristate and phorbol 13-acetate. phorbol 74-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-43 2358463-7 1990 The down-regulation of the hormone receptor was also induced with another phorbol diester, phorbol 12,13-didecanoate, but not with the phorbol or phorbol monoesters phorbol 12-myristate and phorbol 13-acetate. phorbol 91-98 nuclear receptor subfamily 4 group A member 1 Homo sapiens 27-43 33818022-1 2021 PURPOSE: In this trial, we investigated the efficacy and safety of adjuvant letrozole for hormone receptor (HR)-positive breast cancer. Letrozole 76-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-106 33818022-1 2021 PURPOSE: In this trial, we investigated the efficacy and safety of adjuvant letrozole for hormone receptor (HR)-positive breast cancer. Letrozole 76-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-110 1696136-0 1990 [Interaction of hormone-receptor complexes of triiodothyronine with DNA and RNA]. Triiodothyronine 46-62 nuclear receptor subfamily 4 group A member 1 Homo sapiens 16-32 33971386-1 2021 BACKGROUND: Neratinib is approved in the European Union for extended adjuvant treatment of human epidermal growth factor receptor 2-positive/hormone receptor-positive (copositive) early breast cancer <=1 year of completion of prior trastuzumab-based therapy. neratinib 12-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 141-157 33822619-7 2021 The dominant initiation paths for N4, N8, and N10 occur in the heterocycle and in the bond between the heterocycle and azo group, while that for N11 is ring elimination. anthrone 119-122 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-49 33237560-5 2021 In the research, PTE accumulation was determined in the samples of N1 (Pb, As, and Hg), N9 (Cd, As), and N10 (Cd and As) and N8 (Pb) in wheat. pte 17-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-108 33805613-1 2021 Tamoxifen is an endocrine treatment for hormone receptor positive breast cancer. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-56 33796150-1 2021 Background: The CDK4/6 inhibitor palbociclib combined with endocrine therapy (ET) has proven to prolong progression-free survival (PFS) in women with hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer (MBC). palbociclib 33-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-166 33237560-5 2021 In the research, PTE accumulation was determined in the samples of N1 (Pb, As, and Hg), N9 (Cd, As), and N10 (Cd and As) and N8 (Pb) in wheat. Cadmium 110-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 105-108 33034801-8 2021 RESULTS: Equol showed bi-phasic protumor and antitumor effects; at a low concentration, it promoted the tumor growth in hormone receptor-positive cell lines, whereas antitumor effects were generally observed when an excessive amount of dose unexpected in the blood and the tissue was administered. Equol 9-14 nuclear receptor subfamily 4 group A member 1 Homo sapiens 120-136 33235235-9 2020 Dexamethasone upregulated TGFBR1, and TGFBR2 in the presence of TGF-beta1 and increased active NR4A1. Dexamethasone 0-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 95-100 33235235-12 2020 Dexamethasone exhibited diverse regulation of gene expression including NR4A1 upregulation consistent with the anti-fibrotic potential of GCs. Dexamethasone 0-13 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-77 34558047-3 2022 In this work, the interaction quantitative model between resonance light scattering intensity and the concentration of binary surfactant mixtures NP-10+SDBS and NP-10+CTAB was established, and the mechanism of binary surfactant interaction was explored through the model by the resonance light scattering method. Cetrimonium 167-171 nuclear receptor subfamily 4 group A member 1 Homo sapiens 146-151 34558047-3 2022 In this work, the interaction quantitative model between resonance light scattering intensity and the concentration of binary surfactant mixtures NP-10+SDBS and NP-10+CTAB was established, and the mechanism of binary surfactant interaction was explored through the model by the resonance light scattering method. Cetrimonium 167-171 nuclear receptor subfamily 4 group A member 1 Homo sapiens 161-166 34868362-13 2022 ALC is a strong and easy-to-use dosage with prognostic factor for patients with HR+/HER2- mBC treated with palbociclib and endocrine therapy. palbociclib 107-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-82 34463889-0 2022 Successful treatment of a case of hormone receptor-positive metastatic extramammary Paget disease with tamoxifen. Tamoxifen 103-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 34-50 34699643-3 2022 Similar results were observed in these same cell lines after treatment with bisindole-derived (CDIMs) NR4A1 antagonists. bisindole 76-85 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-107 34773204-6 2022 Through decidualization induction of the human endometrial stromal cells (hESCs) cultured in vitro and additional P treatment, the results of chromatin immunoprecipitation and other experiments show that the P treatment could upregulate the expression of NR4A1 in hESCs, and this process was mediated under the direct effect of progesterone receptor (PR) and NR4A1. Progesterone 114-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 255-260 34773204-6 2022 Through decidualization induction of the human endometrial stromal cells (hESCs) cultured in vitro and additional P treatment, the results of chromatin immunoprecipitation and other experiments show that the P treatment could upregulate the expression of NR4A1 in hESCs, and this process was mediated under the direct effect of progesterone receptor (PR) and NR4A1. Progesterone 114-115 nuclear receptor subfamily 4 group A member 1 Homo sapiens 359-364 34773204-6 2022 Through decidualization induction of the human endometrial stromal cells (hESCs) cultured in vitro and additional P treatment, the results of chromatin immunoprecipitation and other experiments show that the P treatment could upregulate the expression of NR4A1 in hESCs, and this process was mediated under the direct effect of progesterone receptor (PR) and NR4A1. Progesterone 208-209 nuclear receptor subfamily 4 group A member 1 Homo sapiens 255-260 34773204-6 2022 Through decidualization induction of the human endometrial stromal cells (hESCs) cultured in vitro and additional P treatment, the results of chromatin immunoprecipitation and other experiments show that the P treatment could upregulate the expression of NR4A1 in hESCs, and this process was mediated under the direct effect of progesterone receptor (PR) and NR4A1. Progesterone 208-209 nuclear receptor subfamily 4 group A member 1 Homo sapiens 359-364 34773204-7 2022 When the NR4A1 in hESCs was silenced, the promotion of hESC proliferation by P was inhibited. Progesterone 77-78 nuclear receptor subfamily 4 group A member 1 Homo sapiens 9-14 34773204-9 2022 The results of spheroid adhesion assay show that the silent NR4A1 had reduced the adhesion of decidual hESCs induced in vitro to embryo. hescs 103-108 nuclear receptor subfamily 4 group A member 1 Homo sapiens 60-65 34931843-1 2021 The dynamics of exciton and free-carrier relaxation of low-dimensional tin iodide perovskites, BA2FAn-1SnnI3n+1, where n = 1 (N1), 2 (N2), 5 (N5), and 10 (N10), were investigated with femtosecond transient absorption spectra (TAS). tin iodide perovskites 71-93 nuclear receptor subfamily 4 group A member 1 Homo sapiens 155-158 34965945-1 2022 PURPOSE: Ribociclib plus endocrine therapy (ET) demonstrated a statistically significant progression-free survival and overall survival (OS) benefit in the phase 3 MONALEESA-7 trial of pre-/perimenopausal patients with hormone-receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer (ABC). ribociclib 9-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 219-235 34965945-1 2022 PURPOSE: Ribociclib plus endocrine therapy (ET) demonstrated a statistically significant progression-free survival and overall survival (OS) benefit in the phase 3 MONALEESA-7 trial of pre-/perimenopausal patients with hormone-receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer (ABC). ribociclib 9-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 237-239 34953442-0 2022 Treatment with ribociclib shows favourable immunomodulatory effects in patients with hormone receptor-positive breast cancer-findings from the RIBECCA trial. ribociclib 15-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 34906197-2 2021 Based on some of their functional and gene modifying activities as anticancer agents, we hypothesized that kaempferol and quercetin were nuclear receptor 4A1 (NR4A1, Nur77) ligands and confirmed that both compounds directly bound NR4A1 with KD values of 3.1 and 0.93 muM, respectively. kaempferol 107-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-171 34906197-2 2021 Based on some of their functional and gene modifying activities as anticancer agents, we hypothesized that kaempferol and quercetin were nuclear receptor 4A1 (NR4A1, Nur77) ligands and confirmed that both compounds directly bound NR4A1 with KD values of 3.1 and 0.93 muM, respectively. kaempferol 107-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 230-235 34906197-0 2021 Flavonoids kaempferol and quercetin are nuclear receptor 4A1 (NR4A1, Nur77) ligands and inhibit rhabdomyosarcoma cell and tumor growth. Flavonoids 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-60 34906197-2 2021 Based on some of their functional and gene modifying activities as anticancer agents, we hypothesized that kaempferol and quercetin were nuclear receptor 4A1 (NR4A1, Nur77) ligands and confirmed that both compounds directly bound NR4A1 with KD values of 3.1 and 0.93 muM, respectively. Quercetin 122-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-157 34906197-0 2021 Flavonoids kaempferol and quercetin are nuclear receptor 4A1 (NR4A1, Nur77) ligands and inhibit rhabdomyosarcoma cell and tumor growth. Flavonoids 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 34906197-0 2021 Flavonoids kaempferol and quercetin are nuclear receptor 4A1 (NR4A1, Nur77) ligands and inhibit rhabdomyosarcoma cell and tumor growth. Flavonoids 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-74 34906197-2 2021 Based on some of their functional and gene modifying activities as anticancer agents, we hypothesized that kaempferol and quercetin were nuclear receptor 4A1 (NR4A1, Nur77) ligands and confirmed that both compounds directly bound NR4A1 with KD values of 3.1 and 0.93 muM, respectively. Quercetin 122-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-164 34906197-0 2021 Flavonoids kaempferol and quercetin are nuclear receptor 4A1 (NR4A1, Nur77) ligands and inhibit rhabdomyosarcoma cell and tumor growth. kaempferol 11-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-60 34906197-0 2021 Flavonoids kaempferol and quercetin are nuclear receptor 4A1 (NR4A1, Nur77) ligands and inhibit rhabdomyosarcoma cell and tumor growth. kaempferol 11-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 34906197-2 2021 Based on some of their functional and gene modifying activities as anticancer agents, we hypothesized that kaempferol and quercetin were nuclear receptor 4A1 (NR4A1, Nur77) ligands and confirmed that both compounds directly bound NR4A1 with KD values of 3.1 and 0.93 muM, respectively. Quercetin 122-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-171 34906197-0 2021 Flavonoids kaempferol and quercetin are nuclear receptor 4A1 (NR4A1, Nur77) ligands and inhibit rhabdomyosarcoma cell and tumor growth. kaempferol 11-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-74 34906197-2 2021 Based on some of their functional and gene modifying activities as anticancer agents, we hypothesized that kaempferol and quercetin were nuclear receptor 4A1 (NR4A1, Nur77) ligands and confirmed that both compounds directly bound NR4A1 with KD values of 3.1 and 0.93 muM, respectively. Quercetin 122-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 230-235 34906197-0 2021 Flavonoids kaempferol and quercetin are nuclear receptor 4A1 (NR4A1, Nur77) ligands and inhibit rhabdomyosarcoma cell and tumor growth. Quercetin 26-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-60 34906197-3 2021 METHODS: The activities of kaempferol and quercetin were determined in direct binding to NR4A1 protein and in NR4A1-dependent transactivation assays in Rh30 and Rh41 rhabdomyosarcoma (RMS) cells. kaempferol 27-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 34906197-0 2021 Flavonoids kaempferol and quercetin are nuclear receptor 4A1 (NR4A1, Nur77) ligands and inhibit rhabdomyosarcoma cell and tumor growth. Quercetin 26-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-67 34906197-0 2021 Flavonoids kaempferol and quercetin are nuclear receptor 4A1 (NR4A1, Nur77) ligands and inhibit rhabdomyosarcoma cell and tumor growth. Quercetin 26-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 69-74 34906197-3 2021 METHODS: The activities of kaempferol and quercetin were determined in direct binding to NR4A1 protein and in NR4A1-dependent transactivation assays in Rh30 and Rh41 rhabdomyosarcoma (RMS) cells. kaempferol 27-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-115 34906197-2 2021 Based on some of their functional and gene modifying activities as anticancer agents, we hypothesized that kaempferol and quercetin were nuclear receptor 4A1 (NR4A1, Nur77) ligands and confirmed that both compounds directly bound NR4A1 with KD values of 3.1 and 0.93 muM, respectively. kaempferol 107-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-157 34906197-3 2021 METHODS: The activities of kaempferol and quercetin were determined in direct binding to NR4A1 protein and in NR4A1-dependent transactivation assays in Rh30 and Rh41 rhabdomyosarcoma (RMS) cells. Quercetin 42-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 89-94 34906197-2 2021 Based on some of their functional and gene modifying activities as anticancer agents, we hypothesized that kaempferol and quercetin were nuclear receptor 4A1 (NR4A1, Nur77) ligands and confirmed that both compounds directly bound NR4A1 with KD values of 3.1 and 0.93 muM, respectively. kaempferol 107-117 nuclear receptor subfamily 4 group A member 1 Homo sapiens 159-164 34906197-3 2021 METHODS: The activities of kaempferol and quercetin were determined in direct binding to NR4A1 protein and in NR4A1-dependent transactivation assays in Rh30 and Rh41 rhabdomyosarcoma (RMS) cells. Quercetin 42-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-115 34906197-6 2021 RESULTS: Kaempferol and quercetin bind NR4A1 protein and inhibit NR4A1-dependent transactivation in RMS cells. kaempferol 9-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 34906197-6 2021 RESULTS: Kaempferol and quercetin bind NR4A1 protein and inhibit NR4A1-dependent transactivation in RMS cells. kaempferol 9-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 65-70 34906197-6 2021 RESULTS: Kaempferol and quercetin bind NR4A1 protein and inhibit NR4A1-dependent transactivation in RMS cells. Quercetin 24-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 34906197-6 2021 RESULTS: Kaempferol and quercetin bind NR4A1 protein and inhibit NR4A1-dependent transactivation in RMS cells. Quercetin 24-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 65-70 34906197-8 2021 The pro-oncogenic PAX3-FOXO1 and G9a genes are also regulated by NR4A1 and, these pathways and genes are all inhibited by kaempferol and quercetin. kaempferol 122-132 nuclear receptor subfamily 4 group A member 1 Homo sapiens 65-70 34906197-8 2021 The pro-oncogenic PAX3-FOXO1 and G9a genes are also regulated by NR4A1 and, these pathways and genes are all inhibited by kaempferol and quercetin. Quercetin 137-146 nuclear receptor subfamily 4 group A member 1 Homo sapiens 65-70 34906197-10 2021 CONCLUSION: These results demonstrate the clinical potential for repurposing kaempferol and quercetin for clinical applications as precision medicine for treating RMS patients that express NR4A1 in order to increase the efficacy and decrease dosages of currently used cytotoxic drugs. kaempferol 77-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 189-194 34906197-10 2021 CONCLUSION: These results demonstrate the clinical potential for repurposing kaempferol and quercetin for clinical applications as precision medicine for treating RMS patients that express NR4A1 in order to increase the efficacy and decrease dosages of currently used cytotoxic drugs. Quercetin 92-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 189-194 34324367-1 2021 PURPOSE: To update recommendations of the ASCO systemic therapy for hormone receptor (HR)-positive metastatic breast cancer (MBC) guideline. asco 42-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 68-84 34324367-1 2021 PURPOSE: To update recommendations of the ASCO systemic therapy for hormone receptor (HR)-positive metastatic breast cancer (MBC) guideline. asco 42-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-88 34324367-4 2021 RECOMMENDATIONS: Alpelisib in combination with endocrine therapy (ET) should be offered to postmenopausal patients, and to male patients, with HR-positive, human epidermal growth factor receptor 2 (HER2)-negative, PIK3CA-mutated, ABC, or MBC following prior endocrine therapy with or without a cyclin-dependent kinase (CDK) 4/6 inhibitor. Alpelisib 17-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 143-145 34880407-5 2021 Hormone receptor negative breast cancers are highly aggressive, and are thought to originate from a subtype of epithelial cells called the luminal progenitor. Phenobarbital 139-146 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 34803903-0 2021 The Role of Ki67 in Evaluating Neoadjuvant Endocrine Therapy of Hormone Receptor-Positive Breast Cancer. ki67 12-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 64-80 34480554-4 2021 In phase I/II clinical studies, the efficacy of Z-endoxifen, the active isomer of endoxifen, was evaluated in patients with endocrine-refractory metastatic breast cancer as well as in patients with gynecologic, desmoid and hormone-receptor positive solid tumors, and demonstrated substantial oral bioavailability and promising antitumor activity. 4-hydroxy-N-desmethyltamoxifen 48-59 nuclear receptor subfamily 4 group A member 1 Homo sapiens 223-239 34480554-4 2021 In phase I/II clinical studies, the efficacy of Z-endoxifen, the active isomer of endoxifen, was evaluated in patients with endocrine-refractory metastatic breast cancer as well as in patients with gynecologic, desmoid and hormone-receptor positive solid tumors, and demonstrated substantial oral bioavailability and promising antitumor activity. 4-hydroxy-N-desmethyltamoxifen 82-91 nuclear receptor subfamily 4 group A member 1 Homo sapiens 223-239 34617955-1 2021 Importance: The cyclin-dependent kinase 4 and 6 inhibitor palbociclib in combination with letrozole has become a standard first-line treatment for patients with endocrine-sensitive, hormone receptor-positive, ERBB2-negative advanced breast cancer. palbociclib 58-69 nuclear receptor subfamily 4 group A member 1 Homo sapiens 182-198 34617955-1 2021 Importance: The cyclin-dependent kinase 4 and 6 inhibitor palbociclib in combination with letrozole has become a standard first-line treatment for patients with endocrine-sensitive, hormone receptor-positive, ERBB2-negative advanced breast cancer. Letrozole 90-99 nuclear receptor subfamily 4 group A member 1 Homo sapiens 182-198 34819039-1 2021 BACKGROUND: Entinostat is an oral inhibitor of class I histone deacetylases intended for endocrine therapy-resistant patients with hormone receptor-positive (HR+) advanced or metastatic breast cancer (BC). entinostat 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 131-147 34844978-0 2022 A randomized trial of fulvestrant, everolimus and anastrozole for the front-line treatment of patients with advanced hormone receptor-positive breast cancer, SWOG S1222. Anastrozole 50-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 117-133 34868931-1 2021 Tamoxifen (TAM) is the most commonly used adjuvant endocrine drug for hormone receptor-positive (HR+) breast cancer patients. Tamoxifen 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-86 34868931-1 2021 Tamoxifen (TAM) is the most commonly used adjuvant endocrine drug for hormone receptor-positive (HR+) breast cancer patients. Tamoxifen 11-14 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-86 34830790-4 2021 We report that PGRMC1 overexpression resulted in increased proliferation of hormone receptor positive breast cancer cell lines upon treatment with a subgroup of progestins including norethisterone and dydrogesterone that promote PGRMC1-phosphorylation on S181. Norethindrone 182-196 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-92 34830790-4 2021 We report that PGRMC1 overexpression resulted in increased proliferation of hormone receptor positive breast cancer cell lines upon treatment with a subgroup of progestins including norethisterone and dydrogesterone that promote PGRMC1-phosphorylation on S181. Dydrogesterone 201-215 nuclear receptor subfamily 4 group A member 1 Homo sapiens 76-92 34830800-3 2021 RECENT FINDINGS: Tamoxifen, aromatase inhibitors, and fulvestrant are the main drugs that have been used for decades in the therapy of hormone-receptor-positive breast cancer patients. Tamoxifen 17-26 nuclear receptor subfamily 4 group A member 1 Homo sapiens 135-151 34754095-1 2022 BACKGROUND: The benefit of alpelisib in hormone-receptor-positive (HR+) metastatic breast cancer patients provided clinical evidence for the increasing importance of PIK3CA testing. Alpelisib 27-36 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-56 34402131-15 2021 IMPLICATIONS FOR PRACTICE: The hormone receptor (HRc) subtype was an independent prognostic factor and the estrogen receptor (ER)+/progesterone receptor (PR)+ subtype showed a better survival in ductal carcinoma in situ (DCIS) patients who received tamoxifen therapy. Tamoxifen 249-258 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-47 34452975-0 2021 Metformin prevents hyperglycaemia-associated, oxidative stress-induced vascular endothelial dysfunction: essential role for the orphan nuclear receptor, Nr4a1 (Nur77). Metformin 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-158 34452975-0 2021 Metformin prevents hyperglycaemia-associated, oxidative stress-induced vascular endothelial dysfunction: essential role for the orphan nuclear receptor, Nr4a1 (Nur77). Metformin 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 160-165 34452975-5 2021 Using in silico modelling of metformin-NR4A1 interactions, Nr4a1-mutagenesis and a transfected HEK 293T cell functional assay for metformin-activated Nr4a1, we identified two Nr4a1 prolines, P505/P549 (mouse sequences corresponding to human P501/P546), as key residues for enabling metformin to affect mitochondrial function. Metformin 29-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 34452975-5 2021 Using in silico modelling of metformin-NR4A1 interactions, Nr4a1-mutagenesis and a transfected HEK 293T cell functional assay for metformin-activated Nr4a1, we identified two Nr4a1 prolines, P505/P549 (mouse sequences corresponding to human P501/P546), as key residues for enabling metformin to affect mitochondrial function. Metformin 130-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-155 34452975-5 2021 Using in silico modelling of metformin-NR4A1 interactions, Nr4a1-mutagenesis and a transfected HEK 293T cell functional assay for metformin-activated Nr4a1, we identified two Nr4a1 prolines, P505/P549 (mouse sequences corresponding to human P501/P546), as key residues for enabling metformin to affect mitochondrial function. Metformin 130-139 nuclear receptor subfamily 4 group A member 1 Homo sapiens 175-180 34452975-5 2021 Using in silico modelling of metformin-NR4A1 interactions, Nr4a1-mutagenesis and a transfected HEK 293T cell functional assay for metformin-activated Nr4a1, we identified two Nr4a1 prolines, P505/P549 (mouse sequences corresponding to human P501/P546), as key residues for enabling metformin to affect mitochondrial function. Metformin 282-291 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-44 34452975-5 2021 Using in silico modelling of metformin-NR4A1 interactions, Nr4a1-mutagenesis and a transfected HEK 293T cell functional assay for metformin-activated Nr4a1, we identified two Nr4a1 prolines, P505/P549 (mouse sequences corresponding to human P501/P546), as key residues for enabling metformin to affect mitochondrial function. Metformin 282-291 nuclear receptor subfamily 4 group A member 1 Homo sapiens 59-64 34452975-5 2021 Using in silico modelling of metformin-NR4A1 interactions, Nr4a1-mutagenesis and a transfected HEK 293T cell functional assay for metformin-activated Nr4a1, we identified two Nr4a1 prolines, P505/P549 (mouse sequences corresponding to human P501/P546), as key residues for enabling metformin to affect mitochondrial function. Metformin 282-291 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-155 34452975-5 2021 Using in silico modelling of metformin-NR4A1 interactions, Nr4a1-mutagenesis and a transfected HEK 293T cell functional assay for metformin-activated Nr4a1, we identified two Nr4a1 prolines, P505/P549 (mouse sequences corresponding to human P501/P546), as key residues for enabling metformin to affect mitochondrial function. Metformin 282-291 nuclear receptor subfamily 4 group A member 1 Homo sapiens 175-180 34452975-6 2021 Our data indicate a critical role for Nr4a1 in metformin"s endothelial-protective effects, observed at micromolar concentrations, which activate AMPKinase but do not affect mitochondrial complex-I or complex-III oxygen consumption rates, as does 0.5 mM metformin. Metformin 47-56 nuclear receptor subfamily 4 group A member 1 Homo sapiens 38-43 34452975-7 2021 Thus, therapeutic metformin concentrations, requiring the expression of Nr4a1, protect the vasculature from hyperglycaemia-induced dysfunction in addition to metformin"s action to enhance insulin action in diabetics. Metformin 18-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 72-77 34452975-10 2021 However, this action of metformin requires the expression of the orphan nuclear receptor, NR4A1/Nur77. Metformin 24-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-95 34452975-10 2021 However, this action of metformin requires the expression of the orphan nuclear receptor, NR4A1/Nur77. Metformin 24-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 96-101 34383180-5 2021 Hormone receptor positivity was defined as estrogen receptor-positive, progesterone-positive and HER 2-negative cancer. Progesterone 71-83 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 34529000-12 2021 Investigational treatments significantly lowered RCB in HR-negative/ERBB2-negative (graduated and nongraduated treatments) and ERBB2-positive subtypes (graduated treatments), with improved EFS (HZR, 0.61; 95% CI, 0.41-0.93) in the exploratory analysis. rcb 49-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 56-58 34402131-15 2021 IMPLICATIONS FOR PRACTICE: The hormone receptor (HRc) subtype was an independent prognostic factor and the estrogen receptor (ER)+/progesterone receptor (PR)+ subtype showed a better survival in ductal carcinoma in situ (DCIS) patients who received tamoxifen therapy. Tamoxifen 249-258 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-52 34745997-0 2021 Which Clinicopathologic Parameters Suggest Primary Resistance to Palbociclib in Combination With Letrozole as the First-Line Treatment for Hormone Receptor-Positive, HER2-Negative Advanced Breast Cancer? palbociclib 65-76 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-155 34745997-0 2021 Which Clinicopathologic Parameters Suggest Primary Resistance to Palbociclib in Combination With Letrozole as the First-Line Treatment for Hormone Receptor-Positive, HER2-Negative Advanced Breast Cancer? Letrozole 97-106 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-155 34745997-1 2021 In this study, we evaluated clinical parameters to predict the primary resistance of palbociclib in combination with endocrine therapy as the first-line treatment in patients with hormone receptor (HR)+, human epidermal growth factor receptor 2 (HER2)- metastatic breast cancer (MBC). palbociclib 85-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 180-202 34720808-7 2021 However, 15 of the HR+ patients died before tamoxifen became available in 2013. Tamoxifen 44-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 19-21 34077833-4 2021 Both PGE2 release and nitric oxide production in macrophage cells were significantly suppressed by the N8 and N10 treatment groups. Dinoprostone 5-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-113 34077833-4 2021 Both PGE2 release and nitric oxide production in macrophage cells were significantly suppressed by the N8 and N10 treatment groups. Nitric Oxide 22-34 nuclear receptor subfamily 4 group A member 1 Homo sapiens 110-113 34629883-0 2021 Ethyl 2-(2,3,4-Trimethoxy-6-(1-Octanoyl)Phenyl) Acetate (TMPA) Ameliorates Lipid Accumulation by Disturbing the Combination of LKB1 with Nur77 and Activating the AMPK Pathway in HepG2 Cells and Mice Primary Hepatocytes. tmpa 57-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-142 34629883-2 2021 Ethyl 2-(2,3,4-trimethoxy-6-(1-octanoyl)phenyl) acetate (TMPA) is a novel AMPK agonist, which influences the stability of Nuclear Receptor Subfamily 4, Group A, Member 1 (Nur77)-serine-threonine kinase 11 (LKB1) in the nucleus. ethyl 2-(2,3,4-trimethoxy-6-(1-octanoyl)phenyl)acetate 0-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-169 34629883-2 2021 Ethyl 2-(2,3,4-trimethoxy-6-(1-octanoyl)phenyl) acetate (TMPA) is a novel AMPK agonist, which influences the stability of Nuclear Receptor Subfamily 4, Group A, Member 1 (Nur77)-serine-threonine kinase 11 (LKB1) in the nucleus. ethyl 2-(2,3,4-trimethoxy-6-(1-octanoyl)phenyl)acetate 0-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-176 34629883-2 2021 Ethyl 2-(2,3,4-trimethoxy-6-(1-octanoyl)phenyl) acetate (TMPA) is a novel AMPK agonist, which influences the stability of Nuclear Receptor Subfamily 4, Group A, Member 1 (Nur77)-serine-threonine kinase 11 (LKB1) in the nucleus. tmpa 57-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 122-169 34629883-2 2021 Ethyl 2-(2,3,4-trimethoxy-6-(1-octanoyl)phenyl) acetate (TMPA) is a novel AMPK agonist, which influences the stability of Nuclear Receptor Subfamily 4, Group A, Member 1 (Nur77)-serine-threonine kinase 11 (LKB1) in the nucleus. tmpa 57-61 nuclear receptor subfamily 4 group A member 1 Homo sapiens 171-176 34629883-14 2021 Conclusion: TMPA ameliorated lipid accumulation by influencing the stability of Nur77-LKB1 in vitro. tmpa 12-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 80-85 34720529-5 2021 Several studies show that drugs targeting Sp downregulation or NR4A1 antagonists are highly effective inhibitors of Sp/NR4A1-regulated pathways and genes in pancreatic and other cancer cells, and the triterpenoid celastrol is a novel dual-acting agent that targets both Sp TFs and NR4A1. sp 42-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-124 34720529-5 2021 Several studies show that drugs targeting Sp downregulation or NR4A1 antagonists are highly effective inhibitors of Sp/NR4A1-regulated pathways and genes in pancreatic and other cancer cells, and the triterpenoid celastrol is a novel dual-acting agent that targets both Sp TFs and NR4A1. sp 116-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 34720529-5 2021 Several studies show that drugs targeting Sp downregulation or NR4A1 antagonists are highly effective inhibitors of Sp/NR4A1-regulated pathways and genes in pancreatic and other cancer cells, and the triterpenoid celastrol is a novel dual-acting agent that targets both Sp TFs and NR4A1. sp 116-118 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-124 34720529-5 2021 Several studies show that drugs targeting Sp downregulation or NR4A1 antagonists are highly effective inhibitors of Sp/NR4A1-regulated pathways and genes in pancreatic and other cancer cells, and the triterpenoid celastrol is a novel dual-acting agent that targets both Sp TFs and NR4A1. Triterpenes 200-212 nuclear receptor subfamily 4 group A member 1 Homo sapiens 281-286 34720529-5 2021 Several studies show that drugs targeting Sp downregulation or NR4A1 antagonists are highly effective inhibitors of Sp/NR4A1-regulated pathways and genes in pancreatic and other cancer cells, and the triterpenoid celastrol is a novel dual-acting agent that targets both Sp TFs and NR4A1. celastrol 213-222 nuclear receptor subfamily 4 group A member 1 Homo sapiens 63-68 34720529-5 2021 Several studies show that drugs targeting Sp downregulation or NR4A1 antagonists are highly effective inhibitors of Sp/NR4A1-regulated pathways and genes in pancreatic and other cancer cells, and the triterpenoid celastrol is a novel dual-acting agent that targets both Sp TFs and NR4A1. celastrol 213-222 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-124 34720529-5 2021 Several studies show that drugs targeting Sp downregulation or NR4A1 antagonists are highly effective inhibitors of Sp/NR4A1-regulated pathways and genes in pancreatic and other cancer cells, and the triterpenoid celastrol is a novel dual-acting agent that targets both Sp TFs and NR4A1. celastrol 213-222 nuclear receptor subfamily 4 group A member 1 Homo sapiens 281-286 34645818-0 2021 Phase separation of Nur77 mediates celastrol-induced mitophagy by promoting the liquidity of p62/SQSTM1 condensates. celastrol 35-44 nuclear receptor subfamily 4 group A member 1 Homo sapiens 20-25 34645818-3 2021 We previously discovered that nuclear receptor Nur77 (also called TR3, NGFI-B, or NR4A1) translocates from the nucleus to mitochondria to mediate celastrol-induced mitophagy through interaction with p62/SQSTM1. celastrol 146-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 47-52 34645818-3 2021 We previously discovered that nuclear receptor Nur77 (also called TR3, NGFI-B, or NR4A1) translocates from the nucleus to mitochondria to mediate celastrol-induced mitophagy through interaction with p62/SQSTM1. celastrol 146-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 66-69 34645818-3 2021 We previously discovered that nuclear receptor Nur77 (also called TR3, NGFI-B, or NR4A1) translocates from the nucleus to mitochondria to mediate celastrol-induced mitophagy through interaction with p62/SQSTM1. celastrol 146-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 71-77 34645818-3 2021 We previously discovered that nuclear receptor Nur77 (also called TR3, NGFI-B, or NR4A1) translocates from the nucleus to mitochondria to mediate celastrol-induced mitophagy through interaction with p62/SQSTM1. celastrol 146-155 nuclear receptor subfamily 4 group A member 1 Homo sapiens 82-87 34645818-4 2021 Here, we show that the ubiquitinated mitochondrial Nur77 forms membraneless condensates capable of sequestrating damaged mitochondria by interacting with the UBA domain of p62/SQSTM1. UBP 310 158-161 nuclear receptor subfamily 4 group A member 1 Homo sapiens 51-56 34740541-0 2022 Real-World Outcomes of Everolimus and Exemestane for the Treatment of Metastatic Hormone Receptor-Positive Breast Cancer in Patients Previously Treated With CDK4/6 Inhibitors. Everolimus 23-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 34740541-0 2022 Real-World Outcomes of Everolimus and Exemestane for the Treatment of Metastatic Hormone Receptor-Positive Breast Cancer in Patients Previously Treated With CDK4/6 Inhibitors. exemestane 38-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 34740541-1 2022 PURPOSE: Everolimus with exemestane (EVE+EXE) was FDA-approved to treat metastatic hormone receptor-positive breast cancer (mHRBC) based on BOLERO-2. Everolimus 9-19 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-99 34740541-1 2022 PURPOSE: Everolimus with exemestane (EVE+EXE) was FDA-approved to treat metastatic hormone receptor-positive breast cancer (mHRBC) based on BOLERO-2. exemestane 25-35 nuclear receptor subfamily 4 group A member 1 Homo sapiens 83-99 34692469-5 2021 Herein, we report the clinical history of a young woman with HR-positive HER2-negative metastatic BC and a pancytopenia due to carcinomatosis of the bone marrow receiving letrozole and leuprorelin plus the CDK4/6 inhibitor palbociclib, who significantly derived clinical benefit from treatment. Letrozole 171-180 nuclear receptor subfamily 4 group A member 1 Homo sapiens 61-63 34692469-5 2021 Herein, we report the clinical history of a young woman with HR-positive HER2-negative metastatic BC and a pancytopenia due to carcinomatosis of the bone marrow receiving letrozole and leuprorelin plus the CDK4/6 inhibitor palbociclib, who significantly derived clinical benefit from treatment. palbociclib 223-234 nuclear receptor subfamily 4 group A member 1 Homo sapiens 61-63 34629883-0 2021 Ethyl 2-(2,3,4-Trimethoxy-6-(1-Octanoyl)Phenyl) Acetate (TMPA) Ameliorates Lipid Accumulation by Disturbing the Combination of LKB1 with Nur77 and Activating the AMPK Pathway in HepG2 Cells and Mice Primary Hepatocytes. ethyl 2-(2,3,4-trimethoxy-6-(1-octanoyl)phenyl)acetate 0-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-142 34805355-0 2021 Efficacy and safety of low-dose everolimus combined with endocrine drugs for patients with hormone receptor-positive, human epidermal growth factor receptor 2-negative metastatic breast cancer. Everolimus 32-42 nuclear receptor subfamily 4 group A member 1 Homo sapiens 91-107 34805355-1 2021 Background: To analyze the efficacy and safety of everolimus 5 mg/day in combination with endocrine drugs in the treatment of hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer using real-world clinical data. Everolimus 50-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 126-142 34805355-2 2021 Methods: Clinical data of hormone receptor (HR)-positive and HER2-negative patients with advanced breast cancer treated with everolimus combined with endocrine drugs in our center between August 2012 and May 2017 were retrospectively analyzed. Everolimus 125-135 nuclear receptor subfamily 4 group A member 1 Homo sapiens 26-48 34805355-11 2021 Conclusions: Our results showed that everolimus (5 mg/day) combined with endocrine therapy was effective and relatively safe for patients with hormone receptor-positive, HER2-negative metastatic breast cancer. Everolimus 37-47 nuclear receptor subfamily 4 group A member 1 Homo sapiens 143-159 34486957-0 2022 From clinical trials to clinical practice: the use of everolimus and exemestane in the treatment of hormone receptor-positive metastatic breast cancer: real-world data. Everolimus 54-64 nuclear receptor subfamily 4 group A member 1 Homo sapiens 100-116 34657059-0 2021 (A Case of Advanced Late Recurrence of Hormone Receptor Positive Breast Cancer Successfully Treated with Abemaciclib and Anastrozole). abemaciclib 105-116 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-55 34657059-0 2021 (A Case of Advanced Late Recurrence of Hormone Receptor Positive Breast Cancer Successfully Treated with Abemaciclib and Anastrozole). Anastrozole 121-132 nuclear receptor subfamily 4 group A member 1 Homo sapiens 39-55 34357781-0 2021 E2112: Randomized Phase III Trial of Endocrine Therapy Plus Entinostat or Placebo in Hormone Receptor-Positive Advanced Breast Cancer. e2112 0-5 nuclear receptor subfamily 4 group A member 1 Homo sapiens 85-101 34436536-2 2021 Objective: To compare the effectiveness of everolimus plus letrozole vs letrozole alone in premenopausal women with HR-positive/ERBB2-negative advanced breast cancer who experienced disease progression while receiving SERMs. Everolimus 43-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 116-118 34436536-2 2021 Objective: To compare the effectiveness of everolimus plus letrozole vs letrozole alone in premenopausal women with HR-positive/ERBB2-negative advanced breast cancer who experienced disease progression while receiving SERMs. Letrozole 59-68 nuclear receptor subfamily 4 group A member 1 Homo sapiens 116-118 34436536-2 2021 Objective: To compare the effectiveness of everolimus plus letrozole vs letrozole alone in premenopausal women with HR-positive/ERBB2-negative advanced breast cancer who experienced disease progression while receiving SERMs. Letrozole 72-81 nuclear receptor subfamily 4 group A member 1 Homo sapiens 116-118 34436536-14 2021 Conclusions and Relevance: In this randomized clinical trial, PFS was significantly longer among premenopausal patients with HR-positive/ERBB2-negative advanced breast cancer who received everolimus plus letrozole than among those who received letrozole alone. Everolimus 188-198 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-127 34436536-14 2021 Conclusions and Relevance: In this randomized clinical trial, PFS was significantly longer among premenopausal patients with HR-positive/ERBB2-negative advanced breast cancer who received everolimus plus letrozole than among those who received letrozole alone. Letrozole 204-213 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-127 34543613-18 2021 Sequential endocrine therapy with tamoxifen for 2-3 years followed by letrozole for 5 years should be considered as one of the optimal standard endocrine treatments for postmenopausal patients with hormone receptor-positive breast cancer. Tamoxifen 34-43 nuclear receptor subfamily 4 group A member 1 Homo sapiens 198-214 34543613-18 2021 Sequential endocrine therapy with tamoxifen for 2-3 years followed by letrozole for 5 years should be considered as one of the optimal standard endocrine treatments for postmenopausal patients with hormone receptor-positive breast cancer. Letrozole 70-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 198-214 34753632-0 2022 A Retrospective Analysis of Metronomic Cyclophosphamide, Methotrexate, and Fluorouracil (CMF) Versus Docetaxel and Cyclophosphamide (TC) as Adjuvant Treatment in Early Stage, Hormone Receptor Positive, HER2 Negative Breast Cancer. Cyclophosphamide 115-131 nuclear receptor subfamily 4 group A member 1 Homo sapiens 175-191 34753632-0 2022 A Retrospective Analysis of Metronomic Cyclophosphamide, Methotrexate, and Fluorouracil (CMF) Versus Docetaxel and Cyclophosphamide (TC) as Adjuvant Treatment in Early Stage, Hormone Receptor Positive, HER2 Negative Breast Cancer. Technetium 133-135 nuclear receptor subfamily 4 group A member 1 Homo sapiens 175-191 34514415-0 2021 CPT1A and fatty acid beta-oxidation are essential for tumor cell growth and survival in hormone receptor-positive breast cancer. Fatty Acids 10-20 nuclear receptor subfamily 4 group A member 1 Homo sapiens 88-104 34486957-0 2022 From clinical trials to clinical practice: the use of everolimus and exemestane in the treatment of hormone receptor-positive metastatic breast cancer: real-world data. exemestane 69-79 nuclear receptor subfamily 4 group A member 1 Homo sapiens 100-116 34217908-2 2021 This phase I/II trial was designed to test the safety and efficacy of palbociclib, pembrolizumab and letrozole in women with hormone receptor positive (HR+) human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer (MBC). Letrozole 101-110 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 34628933-0 2021 Significant response to the combination of pyrotinib and letrozole in a patient with metastatic HER2-positive and hormone receptor-positive breast cancer: a case report. pyrotinib 43-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-130 34628933-0 2021 Significant response to the combination of pyrotinib and letrozole in a patient with metastatic HER2-positive and hormone receptor-positive breast cancer: a case report. Letrozole 57-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 114-130 34416161-0 2021 A bacterial bile acid metabolite modulates Treg activity through the nuclear hormone receptor NR4A1. Bile Acids and Salts 12-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 34414958-1 2021 BACKGROUND: Ovarian function suppressor (OFS) plus either tamoxifen (TAM) or aromatase inhibitor (AI) could improve the survival outcome for premenopausal hormone receptor-positive (HR+) breast cancer. Tamoxifen 58-67 nuclear receptor subfamily 4 group A member 1 Homo sapiens 155-171 34196874-0 2021 Phase I Study and Pilot Efficacy Analysis of Entinostat, a Novel Histone Deacetylase Inhibitor, in Chinese Postmenopausal Women with Hormone Receptor-Positive Metastatic Breast Cancer. entinostat 45-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-149 34196874-1 2021 BACKGROUND: Previous clinical trials have demonstrated that entinostat in combination with exemestane had good tolerability and significant clinical efficacy in patients with advanced hormone receptor positive (HR+) and HER2 negative (HER2-) metastatic breast cancer (MBC) in the USA. entinostat 60-70 nuclear receptor subfamily 4 group A member 1 Homo sapiens 184-200 34196874-1 2021 BACKGROUND: Previous clinical trials have demonstrated that entinostat in combination with exemestane had good tolerability and significant clinical efficacy in patients with advanced hormone receptor positive (HR+) and HER2 negative (HER2-) metastatic breast cancer (MBC) in the USA. exemestane 91-101 nuclear receptor subfamily 4 group A member 1 Homo sapiens 184-200 34414958-1 2021 BACKGROUND: Ovarian function suppressor (OFS) plus either tamoxifen (TAM) or aromatase inhibitor (AI) could improve the survival outcome for premenopausal hormone receptor-positive (HR+) breast cancer. Tamoxifen 69-72 nuclear receptor subfamily 4 group A member 1 Homo sapiens 155-171 34146662-9 2021 Atrazine altered genes expression levels of PAX6, TUBB3, NCAM1, GFAP, TH, NR4A1, and GRIA1. Atrazine 0-8 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-79 34602942-1 2021 Background: Fulvestrant 500 mg monotherapy is recommended as the first-line endocrine treatment in postmenopausal women with hormone receptor-positive metastatic breast cancer (MBC). Fulvestrant 12-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 125-141 34323462-9 2021 Molecules such as decazapentacene (N10) exhibit multistability of oxidation state, and this is predicted to promote the redox catalytic properties of the compounds. decazapentacene 18-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 35-38 34532493-6 2021 Here, we present a case of a 50-year-old postmenopausal HER2-positive/HR-positive breast cancer patient who received pyrotinib plus letrozole as a first-line treatment following a diagnosis of left axillary lymph node and double lung metastases after modified radical mastectomy for left breast cancer. pyrotinib 117-126 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-72 34532493-6 2021 Here, we present a case of a 50-year-old postmenopausal HER2-positive/HR-positive breast cancer patient who received pyrotinib plus letrozole as a first-line treatment following a diagnosis of left axillary lymph node and double lung metastases after modified radical mastectomy for left breast cancer. Letrozole 132-141 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-72 34532493-10 2021 Our case indicates that the combined therapy of pyrotinib plus letrozole may/can be a promising treatment option for patients with HER2-positive/HR-positive MBC. pyrotinib 48-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 145-147 34143979-3 2021 DOP increased pathologic complete response (pCR) rates in all HER2-negative (20%-37%), hormone receptor (HR)-positive/HER2-negative (14%-28%), and triple-negative breast cancer (TNBC) (27%-47%). Diethylhexyl Phthalate 0-3 nuclear receptor subfamily 4 group A member 1 Homo sapiens 87-109 34359587-6 2021 In this review, we will discuss the current state of knowledge on the roles of microRNAs and lncRNAs in the main mechanisms of tamoxifen resistance in hormone receptor positive breast cancer. Tamoxifen 127-136 nuclear receptor subfamily 4 group A member 1 Homo sapiens 151-167 34109683-15 2021 We propose that the suppression of the calcium-NFATc3-NR4A1 cascade by these three drugs plays a role in the development of DIGO. digo 124-128 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-59 34109683-14 2021 We confirmed that CsA, NIF, and PHT reduced cytosolic calcium levels increased by TGF-beta, while CaCl2 enhanced the TGF-beta-up-regulated NR4A1 expression. Cyclosporine 18-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 34109683-14 2021 We confirmed that CsA, NIF, and PHT reduced cytosolic calcium levels increased by TGF-beta, while CaCl2 enhanced the TGF-beta-up-regulated NR4A1 expression. Calcium Chloride 98-103 nuclear receptor subfamily 4 group A member 1 Homo sapiens 139-144 34221179-9 2021 The HER2-specific tyrosine kinase inhibitor tucatinib when added to trastuzumab and capecitabine was shown to improve PFS and overall survival (OS) over trastuzumab and capecitabine alone in pretreated patients in the randomized HER2CLIMB trial; this benefit was apparently independent of hormone-receptor expression. Irbinitinib 44-53 nuclear receptor subfamily 4 group A member 1 Homo sapiens 289-305 34109683-15 2021 We propose that the suppression of the calcium-NFATc3-NR4A1 cascade by these three drugs plays a role in the development of DIGO. Calcium 39-46 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-59 34182489-7 2021 RESULTS: A substitution in the NR4A1 gene at codon 293 resulting in an amino acid change from arginine to serine was identified only in the affected sisters. Arginine 94-102 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-36 34182489-7 2021 RESULTS: A substitution in the NR4A1 gene at codon 293 resulting in an amino acid change from arginine to serine was identified only in the affected sisters. Serine 106-112 nuclear receptor subfamily 4 group A member 1 Homo sapiens 31-36 34209871-0 2021 NR4A1 Regulates Tamoxifen Resistance by Suppressing ERK Signaling in ER-Positive Breast Cancer. Tamoxifen 16-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 34096894-1 2021 OBJECTIVES: Letrozole is a nonsteroidal aromatase inhibitor used to treat hormone-receptor-positive breast cancer. Letrozole 12-21 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-90 34096894-4 2021 METHODS: The Exemestane and Letrozole Pharmacogenetics (ELPh) Study randomized postmenopausal patients with hormone-receptor-positive nonmetastatic breast cancer to letrozole or exemestane treatment. exemestane 13-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-124 34096894-4 2021 METHODS: The Exemestane and Letrozole Pharmacogenetics (ELPh) Study randomized postmenopausal patients with hormone-receptor-positive nonmetastatic breast cancer to letrozole or exemestane treatment. Letrozole 28-37 nuclear receptor subfamily 4 group A member 1 Homo sapiens 108-124 34209871-6 2021 Here, we propose that NR4A1 is a promising target to overcome tamoxifen resistance. Tamoxifen 62-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 22-27 34209871-7 2021 NR4A1 gene expression was downregulated in tamoxifen-resistant MCF7 (TamR) cells compared to that in MCF7 cells. Tamoxifen 43-52 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-5 34209871-8 2021 Kaplan-Meier plots were used to identify high NR4A1 expression correlated with increased survival rates in patients with ER-positive breast cancer following tamoxifen treatment. Tamoxifen 157-166 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-51 34209871-9 2021 Gain and loss of function experiments showed that NR4A1 restores sensitivity to tamoxifen by regulating cell proliferation, migration, invasion, and apoptosis. Tamoxifen 80-89 nuclear receptor subfamily 4 group A member 1 Homo sapiens 50-55 34209871-11 2021 In silico and in vitro analyses revealed that NR4A1 enhanced responsiveness to tamoxifen by suppressing ERK signaling in ER-positive breast cancer, suggesting that the NR4A1/ERK signaling axis modulates tamoxifen resistance. Tamoxifen 79-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-51 34209871-11 2021 In silico and in vitro analyses revealed that NR4A1 enhanced responsiveness to tamoxifen by suppressing ERK signaling in ER-positive breast cancer, suggesting that the NR4A1/ERK signaling axis modulates tamoxifen resistance. Tamoxifen 79-88 nuclear receptor subfamily 4 group A member 1 Homo sapiens 168-173 34209871-11 2021 In silico and in vitro analyses revealed that NR4A1 enhanced responsiveness to tamoxifen by suppressing ERK signaling in ER-positive breast cancer, suggesting that the NR4A1/ERK signaling axis modulates tamoxifen resistance. Tamoxifen 203-212 nuclear receptor subfamily 4 group A member 1 Homo sapiens 46-51 34209871-11 2021 In silico and in vitro analyses revealed that NR4A1 enhanced responsiveness to tamoxifen by suppressing ERK signaling in ER-positive breast cancer, suggesting that the NR4A1/ERK signaling axis modulates tamoxifen resistance. Tamoxifen 203-212 nuclear receptor subfamily 4 group A member 1 Homo sapiens 168-173 34209871-12 2021 These results indicate that NR4A1 could be a potential therapeutic target to overcome tamoxifen resistance in ER-positive breast cancer. Tamoxifen 86-95 nuclear receptor subfamily 4 group A member 1 Homo sapiens 28-33 34392523-10 2021 Water-related disasters accounted for nearly three-fourths of the natural disasters (hurricanes 40 percent, N = 12; floods, 33.3 percent, N = 10; total 73.3 percent, N = 22), then snow/ice storms (13.3 percent, N = 4). Water 0-5 nuclear receptor subfamily 4 group A member 1 Homo sapiens 138-144 34248473-5 2021 Case Presentation: Here, we describe a female patient with metastatic hormone receptor-positive/human epidermal growth factor 2-negative breast cancer who developed lung toxicity while on ribociclib. ribociclib 188-198 nuclear receptor subfamily 4 group A member 1 Homo sapiens 70-86 34128985-3 2021 Lama5 loss in the keratin 8-expressing cells results in reduced frequency and differentiation of hormone receptor expressing (HR+) luminal cells. Phenobarbital 131-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-113 34150608-12 2021 Conclusions: Our data provide evidence that the emergence of CTC-WBC clusters underwent EMT before treatment is associated with significantly poorer PFS in HR-positive/HER2-negative metastatic breast cancer patients receiving docetaxel plus capecitabine, which may be used as a parameter to predict the clinical outcomes and a potential target for individualized therapy. Docetaxel 226-235 nuclear receptor subfamily 4 group A member 1 Homo sapiens 156-158 34150608-12 2021 Conclusions: Our data provide evidence that the emergence of CTC-WBC clusters underwent EMT before treatment is associated with significantly poorer PFS in HR-positive/HER2-negative metastatic breast cancer patients receiving docetaxel plus capecitabine, which may be used as a parameter to predict the clinical outcomes and a potential target for individualized therapy. Capecitabine 241-253 nuclear receptor subfamily 4 group A member 1 Homo sapiens 156-158 34102639-0 2021 (18F)-Fluorodeoxyglucose Positron Emission Tomography/CT to Assess the Early Metabolic Response in Patients with Hormone Receptor-Positive HER2-Negative Metastasized Breast Cancer Treated with Cyclin-Dependent 4/6 Kinase Inhibitors. Fluorodeoxyglucose F18 0-24 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-129 34259084-1 2021 Alpelisib is a alpha-selective phosphatidylinositol 3-kinase (PI3K) inhibitor approved for treatment of postmenopausal women, and men, with hormone receptor positive (HR+), human epidermal growth factor receptor 2 negative (HER2-), PIK3CA-mutated, advanced breast cancer (ABC). Alpelisib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 140-156 35605174-0 2022 Everolimus Added to Adjuvant Endocrine Therapy in Patients With High-Risk Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Primary Breast Cancer. Everolimus 0-10 nuclear receptor subfamily 4 group A member 1 Homo sapiens 74-90 35597619-0 2022 Everolimus and exemestane in hormone receptor positive advanced breast cancer: A comprehensive cancer center"s experience. exemestane 15-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 29-45 35636320-0 2022 Hormone receptor binding, selectivity and cytotoxicity of steroid D-homo lactone loaded chitosan nanoparticles for the treatment of breast and prostate cancer cells. Chitosan 88-96 nuclear receptor subfamily 4 group A member 1 Homo sapiens 0-16 35398754-5 2022 Phase I/II studies demonstrated greater efficacy when capivasertib was co-administered with paclitaxel, fulvestrant in hormone receptor (HR)-positive, HER2-negative breast cancer or olaparib. capivasertib 54-66 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-141 35567914-2 2022 The CDK 4/6 inhibitor palbociclib has demonstrated efficacy in clinical studies in patients with hormone receptor-positive (HR+), human epidermal growth factor 2 (HER2)-negative advanced/metastatic breast cancer (ABC/MBC). palbociclib 22-33 nuclear receptor subfamily 4 group A member 1 Homo sapiens 97-113 35577139-8 2022 The proliferation index of the luminal B group was significantly (p < 0.001) higher in the low HR (hormone receptor) group than in the HR group. Phenobarbital 31-38 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-115 35579777-1 2022 Patients with hormone receptor (HR)-positive tumors breast cancer usually experience a relatively low pathological complete response (pCR) to neoadjuvant chemotherapy (NAC). nac 168-171 nuclear receptor subfamily 4 group A member 1 Homo sapiens 14-30 35579777-1 2022 Patients with hormone receptor (HR)-positive tumors breast cancer usually experience a relatively low pathological complete response (pCR) to neoadjuvant chemotherapy (NAC). nac 168-171 nuclear receptor subfamily 4 group A member 1 Homo sapiens 32-34 35534752-0 2022 Cost Effectiveness of Ribociclib and Palbociclib in the Second-Line Treatment of Hormone Receptor-Positive, HER2-Negative Metastatic Breast Cancer in Post-Menopausal Indian Women. palbociclib 37-48 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-97 35563670-2 2022 In a previous study, we demonstrated that fangchinoline (FCN), a natural inhibitor of nuclear NR4A1, induces NR4A1-dependent apoptosis in human pancreatic cancer cells. fangchinoline 42-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 35563670-2 2022 In a previous study, we demonstrated that fangchinoline (FCN), a natural inhibitor of nuclear NR4A1, induces NR4A1-dependent apoptosis in human pancreatic cancer cells. fangchinoline 42-55 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-114 35563670-2 2022 In a previous study, we demonstrated that fangchinoline (FCN), a natural inhibitor of nuclear NR4A1, induces NR4A1-dependent apoptosis in human pancreatic cancer cells. fangchinoline 57-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 94-99 35563670-2 2022 In a previous study, we demonstrated that fangchinoline (FCN), a natural inhibitor of nuclear NR4A1, induces NR4A1-dependent apoptosis in human pancreatic cancer cells. fangchinoline 57-60 nuclear receptor subfamily 4 group A member 1 Homo sapiens 109-114 35563670-3 2022 In this study, we evaluated FCN and its structural analogs (berbamine, isotetrandrine, tetrandrine, and tubocurarine) for their inhibitory effects on NR4A1 transactivity, and confirmed that tetrandrine (TTD) showed the highest inhibitory effect in pancreatic cancer cells. fangchinoline 28-31 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-155 35563670-3 2022 In this study, we evaluated FCN and its structural analogs (berbamine, isotetrandrine, tetrandrine, and tubocurarine) for their inhibitory effects on NR4A1 transactivity, and confirmed that tetrandrine (TTD) showed the highest inhibitory effect in pancreatic cancer cells. tetrandrine 190-201 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-155 35563670-3 2022 In this study, we evaluated FCN and its structural analogs (berbamine, isotetrandrine, tetrandrine, and tubocurarine) for their inhibitory effects on NR4A1 transactivity, and confirmed that tetrandrine (TTD) showed the highest inhibitory effect in pancreatic cancer cells. tetrandrine 203-206 nuclear receptor subfamily 4 group A member 1 Homo sapiens 150-155 35563670-4 2022 Moreover, in a tryptophan fluorescence quenching assay, TTD directly bound to the ligand binding domain (LBD) of NR4A1 with a KD value of 10.60 muM. Tryptophan 15-25 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-118 35563670-5 2022 Treatment with TTD decreased proliferation and induced apoptosis in Panc-1 human pancreatic cancer cells in part through the reduced expression of the Sp1-dependent anti-apoptotic gene survivin and induction of ROS-mediated endoplasmic reticulum stress, which are the well-known NR4A1-dependent proapoptotic pathways. tetrandrine 15-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 279-284 35563670-5 2022 Treatment with TTD decreased proliferation and induced apoptosis in Panc-1 human pancreatic cancer cells in part through the reduced expression of the Sp1-dependent anti-apoptotic gene survivin and induction of ROS-mediated endoplasmic reticulum stress, which are the well-known NR4A1-dependent proapoptotic pathways. ros 211-214 nuclear receptor subfamily 4 group A member 1 Homo sapiens 279-284 35530963-13 2022 We also explored the relationship between Celastrol and the nuclear receptor Nur77 and found that it could up-regulate the expression of Nur77. celastrol 42-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 77-82 35478061-3 2022 County-level data from the US national datasets were analyzed for the association between emissions of various metals including arsenic, cadmium, chromium VI, lead, and mercury, and the annual age-adjusted incidence of hormone receptor-dependent breast cancer for 1990-2016 and HER2-dependent breast cancer for 2010-2016 using adjusted linear regression models. Mercury 169-176 nuclear receptor subfamily 4 group A member 1 Homo sapiens 219-235 35530963-13 2022 We also explored the relationship between Celastrol and the nuclear receptor Nur77 and found that it could up-regulate the expression of Nur77. celastrol 42-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 137-142 35000092-0 2022 Factors leading to alpelisib discontinuation in patients with hormone receptor positive, human epidermal growth factor receptor-2 negative breast cancer. Alpelisib 19-28 nuclear receptor subfamily 4 group A member 1 Homo sapiens 62-78 35182885-0 2022 Discovery of a Nur77-mediated cytoplasmic vacuolation and paraptosis inducer (4-PQBH) for the treatment of hepatocellular carcinoma. 4-PQBH 78-84 nuclear receptor subfamily 4 group A member 1 Homo sapiens 15-20 35182885-3 2022 Our recent work demonstrated that certain quinoline-Schiff-base derivatives were good Nur77 mediators that exerted excellent anti-HCC activities in vitro and in vivo. quinoline 42-51 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-91 35182885-3 2022 Our recent work demonstrated that certain quinoline-Schiff-base derivatives were good Nur77 mediators that exerted excellent anti-HCC activities in vitro and in vivo. Schiff Bases 52-63 nuclear receptor subfamily 4 group A member 1 Homo sapiens 86-91 35182885-5 2022 As a continuous work, we synthesized a series of 4-(quinoline-4-amino) benzoylhydrazide derivatives and evaluated their anti-HCC activity and binding affinity to Nur77 in vitro. 4-(quinoline-4-amino) benzoylhydrazide 49-87 nuclear receptor subfamily 4 group A member 1 Homo sapiens 162-167 35182885-6 2022 Compound 4-PQBH emerged as the best Nur77 binder (KD = 1.17 muM) and has potentially selective cytotoxicity to HCC cells. 4-PQBH 9-15 nuclear receptor subfamily 4 group A member 1 Homo sapiens 36-41 35182885-7 2022 Mechanistically, 4-PQBH extensively induced caspase-independent cytoplasmic vacuolization and paraptosis through Nur77-mediated ER stress and autophagy. 4-PQBH 17-23 nuclear receptor subfamily 4 group A member 1 Homo sapiens 113-118 35182885-8 2022 Moreover, 4-PQBH exhibited an effective xenograft tumor inhibition by modulating Nur77-dependent cytoplasmic vacuolation and paraptosis. 4-PQBH 10-16 nuclear receptor subfamily 4 group A member 1 Homo sapiens 81-86 35000092-1 2022 PURPOSE: Alpelisib is a phosphoinositide-3-kinase inhibitor approved for hormone-receptor-positive, PIK3CA-mutated metastatic breast cancer. Alpelisib 9-18 nuclear receptor subfamily 4 group A member 1 Homo sapiens 73-89 35406370-1 2022 Alpelisib is an alpha-selective phosphatidylinositol 3-kinase inhibitor used for treating hormone receptor-positive (HR+), human epidermal growth receptor 2-negative (HER2-), PIK3CA-mutated locally advanced or metastatic breast cancer following disease progression on or after endocrine therapy. Alpelisib 0-9 nuclear receptor subfamily 4 group A member 1 Homo sapiens 90-106 35351974-0 2022 Retraction Note: The nuclear orphan receptor Nur77 alleviates palmitate-induced fat accumulation by down-regulating G0S2 in HepG2 cells. Palmitates 62-71 nuclear receptor subfamily 4 group A member 1 Homo sapiens 45-50 35268797-3 2022 Our previous studies have found that the introduction of bicyclic aromatic rings, such as naphthalyl and quinoline groups, into the N"-methylene position of indoles" Nur77 modulators can effectively improve the anti-tumor activity of the target compounds. naphthalyl 90-100 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-171 35300061-0 2022 Thromboembolic Events in Patients with HER2-Negative, Hormone Receptor-Positive, Metastatic Breast Cancer Treated with Ribociclib Combined with Letrozole or Fulvestrant: A Real-World Data. ribociclib 119-129 nuclear receptor subfamily 4 group A member 1 Homo sapiens 54-70 35268797-3 2022 Our previous studies have found that the introduction of bicyclic aromatic rings, such as naphthalyl and quinoline groups, into the N"-methylene position of indoles" Nur77 modulators can effectively improve the anti-tumor activity of the target compounds. quinoline 105-114 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-171 35268797-3 2022 Our previous studies have found that the introduction of bicyclic aromatic rings, such as naphthalyl and quinoline groups, into the N"-methylene position of indoles" Nur77 modulators can effectively improve the anti-tumor activity of the target compounds. n"-methylene 132-144 nuclear receptor subfamily 4 group A member 1 Homo sapiens 166-171 35268797-0 2022 Synthesis and Biological Evaluation of 1-(2-(6-Methoxynaphthalen-2-yl)-6-methylnicotinoyl)-4-Substituted Semicarbazides/Thiosemicarbazides as Anti-Tumor Nur77 Modulators. 1-(2-(6-methoxynaphthalen-2-yl)-6-methylnicotinoyl)-4-substituted semicarbazides 39-119 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-158 35091347-11 2022 Moreover, we observed that the virulent ST59 and ST22 can resist killing by human antimicrobial peptides (AMPs). Peptides 96-104 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-44 35268797-0 2022 Synthesis and Biological Evaluation of 1-(2-(6-Methoxynaphthalen-2-yl)-6-methylnicotinoyl)-4-Substituted Semicarbazides/Thiosemicarbazides as Anti-Tumor Nur77 Modulators. thiosemicarbazide 120-138 nuclear receptor subfamily 4 group A member 1 Homo sapiens 153-158 35172272-0 2022 Serum thymidine kinase activity in patients with hormone receptor-positive and HER2-negative metastatic breast cancer treated with palbociclib and fulvestrant. palbociclib 131-142 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-65 35172272-0 2022 Serum thymidine kinase activity in patients with hormone receptor-positive and HER2-negative metastatic breast cancer treated with palbociclib and fulvestrant. Fulvestrant 147-158 nuclear receptor subfamily 4 group A member 1 Homo sapiens 49-65 35268797-9 2022 We initially explored the mechanism of 9h-induced apoptosis and found that compound 9h can upregulate Nur77 expression and triggered Nur77 nuclear export, indicating the occurrence of Nur77-mediated apoptosis. 9h 39-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 102-107 35268797-9 2022 We initially explored the mechanism of 9h-induced apoptosis and found that compound 9h can upregulate Nur77 expression and triggered Nur77 nuclear export, indicating the occurrence of Nur77-mediated apoptosis. 9h 39-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 133-138 35268797-9 2022 We initially explored the mechanism of 9h-induced apoptosis and found that compound 9h can upregulate Nur77 expression and triggered Nur77 nuclear export, indicating the occurrence of Nur77-mediated apoptosis. 9h 39-41 nuclear receptor subfamily 4 group A member 1 Homo sapiens 184-189 35220235-6 2022 RESULTS: The disease-free survival (DFS) period after NAC for the high-FF-TIL group was found to be significantly longer than that for the low-FF-TIL group for all cases (p<0.001) and for all subtypes of triple-negative breast cancer (TNBC) (p=0.001), human epidermal growth factor receptor 2-enriched breast cancer (HER2BC) (p=0.010), and hormone receptor-positive breast cancer (HRBC) (p=0.003). nac 54-57 nuclear receptor subfamily 4 group A member 1 Homo sapiens 340-356 34995105-1 2022 PURPOSE: The PALLAS study investigated whether the addition of palbociclib, an oral CDK4/6 inhibitor, to adjuvant endocrine therapy (ET) improves invasive disease-free survival (iDFS) in early hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2-) breast cancer. palbociclib 63-74 nuclear receptor subfamily 4 group A member 1 Homo sapiens 193-209 35091347-11 2022 Moreover, we observed that the virulent ST59 and ST22 can resist killing by human antimicrobial peptides (AMPs). Adenylyl sulfate 106-110 nuclear receptor subfamily 4 group A member 1 Homo sapiens 40-44 35089453-1 2022 BACKGROUND: Everolimus is a mechanistic-target-of-rapamycin (mTOR) inhibitor bearing a potent antitumor effect against hormone receptor-positive breast cancer. Everolimus 12-22 nuclear receptor subfamily 4 group A member 1 Homo sapiens 119-135 34983437-0 2022 Trastuzumab and fulvestrant combination therapy for women with advanced breast cancer positive for hormone receptor and human epidermal growth factor receptor 2: a retrospective single-center study. Fulvestrant 16-27 nuclear receptor subfamily 4 group A member 1 Homo sapiens 99-115