PMID-sentid Pub_year Sent_text compound_name comp_offset prot_official_name organism prot_offset 29932882-9 2018 After treatment with Nutlin, increased nuclear localization of p53 (4.05%-80.56%) was observed in pterygium cells along with increasing Nutlin dosages (from 0 to 50 muM, p < 0.001). nutlin 21-27 tumor protein p53 Homo sapiens 63-66 33216890-2 2020 There is concern, however, that nutlin therapy might stimulate the emergence or expansion of TP53-mutated subclones. nutlin 32-38 tumor protein p53 Homo sapiens 93-97 31036564-8 2019 Further experiments suggested that MDM2 amplification increases histone methylation in Nutlin-treated cells by causing depletion of the histone demethylase Jumonji domain-containing protein 2B (JMJD2B). nutlin 87-93 MDM2 proto-oncogene Homo sapiens 35-39 31036564-8 2019 Further experiments suggested that MDM2 amplification increases histone methylation in Nutlin-treated cells by causing depletion of the histone demethylase Jumonji domain-containing protein 2B (JMJD2B). nutlin 87-93 lysine demethylase 4B Homo sapiens 156-192 31036564-8 2019 Further experiments suggested that MDM2 amplification increases histone methylation in Nutlin-treated cells by causing depletion of the histone demethylase Jumonji domain-containing protein 2B (JMJD2B). nutlin 87-93 lysine demethylase 4B Homo sapiens 194-200 30832755-0 2019 Nutlin-3-induced Sensitization of Non-Small Cell Lung Cancer Stem Cells to Axitinib-Induced Apoptosis through Repression of Akt1/Wnt Signaling. nutlin 0-6 AKT serine/threonine kinase 1 Homo sapiens 124-128 31607444-5 2019 In contrast, P53 induction by Nutlin and Hsp90 inhibitor AUY922 enhanced the BBB function. nutlin 30-36 tumor protein p53 Homo sapiens 13-16 30794402-6 2019 We extracted the binding pocket of Nutlin from the crystal structure of Nutlin bound MDM2. nutlin 35-41 MDM2 proto-oncogene Homo sapiens 85-89 29932882-10 2018 The expression of p21 was increased after Nutlin treatments in pterygium cells (2.49 folds in 20 muM Nutlin treated cells compared to control treated cells, p = 0.012). nutlin 42-48 H3 histone pseudogene 16 Homo sapiens 18-21 26046940-8 2015 By contrast, Nutlin or benzodiazepinedione inhibitors, that bind with similar affinity to full lid and lid-truncated MDM2 constructs, interact additionally through their solubilizing groups with N-terminal lid residues that are more disordered in apo MDM2. nutlin 13-19 MDM2 proto-oncogene Homo sapiens 117-121 26959882-6 2016 We compared its effect to MI-219 and Nutlin, which are less potent MDM2 antagonists than SAR405838. nutlin 37-43 MDM2 proto-oncogene Homo sapiens 67-71 26883108-7 2016 In addition, combined treatment with GSK2830371 and doxorubicin or nutlin-3 potentiated cell death through a strong induction of p53 pathway and activation of caspase 9. nutlin 67-73 tumor protein p53 Homo sapiens 129-132 26883108-7 2016 In addition, combined treatment with GSK2830371 and doxorubicin or nutlin-3 potentiated cell death through a strong induction of p53 pathway and activation of caspase 9. nutlin 67-73 caspase 9 Homo sapiens 159-168 26046940-8 2015 By contrast, Nutlin or benzodiazepinedione inhibitors, that bind with similar affinity to full lid and lid-truncated MDM2 constructs, interact additionally through their solubilizing groups with N-terminal lid residues that are more disordered in apo MDM2. nutlin 13-19 MDM2 proto-oncogene Homo sapiens 251-255 24885082-3 2014 In this study we aimed to investigate the functional role of this p53 acetylation in nutlin-sensitivity, and further to explore if nutlin-induced protein acetylation in general could indicate novel targets for the enhancement of nutlin-based therapy. nutlin 85-91 tumor protein p53 Homo sapiens 66-69 24366007-11 2014 Collectively, these results suggest that nutlin-3 induces HO-1 expression via the activation of both JNK which is dependent on ROS generated by p53 translocated to the mitochondria and p38 MAPK which appears to be stimulated by a ROS-independent mechanism, and this HO-1 induction may inhibit nutlin-3-induced apoptosis, constituting a negative feedback loop of p53-induced apoptosis. nutlin 41-47 mitogen-activated protein kinase 8 Homo sapiens 101-104 24366007-11 2014 Collectively, these results suggest that nutlin-3 induces HO-1 expression via the activation of both JNK which is dependent on ROS generated by p53 translocated to the mitochondria and p38 MAPK which appears to be stimulated by a ROS-independent mechanism, and this HO-1 induction may inhibit nutlin-3-induced apoptosis, constituting a negative feedback loop of p53-induced apoptosis. nutlin 41-47 tumor protein p53 Homo sapiens 144-147 24366007-11 2014 Collectively, these results suggest that nutlin-3 induces HO-1 expression via the activation of both JNK which is dependent on ROS generated by p53 translocated to the mitochondria and p38 MAPK which appears to be stimulated by a ROS-independent mechanism, and this HO-1 induction may inhibit nutlin-3-induced apoptosis, constituting a negative feedback loop of p53-induced apoptosis. nutlin 41-47 mitogen-activated protein kinase 1 Homo sapiens 185-188 24366007-11 2014 Collectively, these results suggest that nutlin-3 induces HO-1 expression via the activation of both JNK which is dependent on ROS generated by p53 translocated to the mitochondria and p38 MAPK which appears to be stimulated by a ROS-independent mechanism, and this HO-1 induction may inhibit nutlin-3-induced apoptosis, constituting a negative feedback loop of p53-induced apoptosis. nutlin 41-47 tumor protein p53 Homo sapiens 362-365 23114582-8 2012 Selective inhibition of these pathways may synergize with nutlin in the induction of p53 transcriptional activity. nutlin 58-64 transformation related protein 53, pseudogene Mus musculus 85-88 23856246-5 2013 Furthermore, we identify pharmacogenomic correlations between specific variants in genes such as TP53, BRAF, ERBBs, and ATAD5 and anticancer agents such as nutlin, vemurafenib, erlotinib, and bleomycin showing one of many ways the data could be used to validate and generate novel hypotheses for further investigation. nutlin 156-162 tumor protein p53 Homo sapiens 97-101 23856246-5 2013 Furthermore, we identify pharmacogenomic correlations between specific variants in genes such as TP53, BRAF, ERBBs, and ATAD5 and anticancer agents such as nutlin, vemurafenib, erlotinib, and bleomycin showing one of many ways the data could be used to validate and generate novel hypotheses for further investigation. nutlin 156-162 B-Raf proto-oncogene, serine/threonine kinase Homo sapiens 103-107 23856246-5 2013 Furthermore, we identify pharmacogenomic correlations between specific variants in genes such as TP53, BRAF, ERBBs, and ATAD5 and anticancer agents such as nutlin, vemurafenib, erlotinib, and bleomycin showing one of many ways the data could be used to validate and generate novel hypotheses for further investigation. nutlin 156-162 ATPase family AAA domain containing 5 Homo sapiens 120-125 22476102-7 2012 Furthermore, adaptation to RITA was associated with fewer changes at the expression level of antiapoptotic factors than observed with adaptation to nutlin-3. nutlin 148-154 zinc finger protein 331 Homo sapiens 27-31 22872685-0 2012 Combination treatment in vitro with Nutlin, a small-molecule antagonist of MDM2, and pegylated interferon-alpha 2a specifically targets JAK2V617F-positive polycythemia vera cells. nutlin 36-42 MDM2 proto-oncogene Homo sapiens 75-79 22578852-11 2012 From these results, we concluded that nutlin-3 has an antitumor effect on feline lymphoma cell lines harboring the wt-p53 gene through accumulation and activation of P53 leading to cell cycle arrest and apoptosis. nutlin 38-44 tumor protein p53 Homo sapiens 118-121 22578852-11 2012 From these results, we concluded that nutlin-3 has an antitumor effect on feline lymphoma cell lines harboring the wt-p53 gene through accumulation and activation of P53 leading to cell cycle arrest and apoptosis. nutlin 38-44 tumor protein p53 Homo sapiens 166-169 20871630-8 2011 p21 was found to mediate nutlin-induced p53-dependent downregulation of another antiapoptotic protein, survivin, without significantly affecting the apoptotic outcome. nutlin 25-31 cyclin dependent kinase inhibitor 1A Homo sapiens 0-3 20871630-8 2011 p21 was found to mediate nutlin-induced p53-dependent downregulation of another antiapoptotic protein, survivin, without significantly affecting the apoptotic outcome. nutlin 25-31 tumor protein p53 Homo sapiens 40-43 19737973-7 2009 Retinoblastoma family members (pRb, p107, and p130) previously implicated in gene silencing during fibroblasts senescence were found down-regulated in cells with nutlin-induced senescence-like phenotype, suggesting a mechanism for its reversibility. nutlin 162-168 RB transcriptional corepressor 1 Homo sapiens 31-34 20424123-10 2010 In contrast, doxorubicin or nutlin-3 treatment-both leading to p53-p21 activation-or CDK2 inhibition had no effect on SKP2 regulation in MYCN-amplified cells. nutlin 28-34 tumor protein p53 Homo sapiens 63-66 20424123-10 2010 In contrast, doxorubicin or nutlin-3 treatment-both leading to p53-p21 activation-or CDK2 inhibition had no effect on SKP2 regulation in MYCN-amplified cells. nutlin 28-34 H3 histone pseudogene 16 Homo sapiens 67-70 20371712-3 2010 Previous studies have reported that Nutlin promotes growth arrest and/or apoptosis in cancer cells that express wild-type p53. nutlin 36-42 tumor protein p53 Homo sapiens 122-125 20371712-9 2010 Taken together, these findings reveal that Nutlin treatment can inhibit the migration and invasion capacity of p53 wild-type cells, adding to the potential therapeutic benefit of Nutlin and other small molecule MDM2 inhibitors. nutlin 43-49 tumor protein p53 Homo sapiens 111-114 20371712-9 2010 Taken together, these findings reveal that Nutlin treatment can inhibit the migration and invasion capacity of p53 wild-type cells, adding to the potential therapeutic benefit of Nutlin and other small molecule MDM2 inhibitors. nutlin 43-49 MDM2 proto-oncogene Homo sapiens 211-215 19903807-0 2009 Antitumor activity of the selective MDM2 antagonist nutlin-3 against chemoresistant neuroblastoma with wild-type p53. nutlin 52-58 transformed mouse 3T3 cell double minute 2 Mus musculus 36-40 19903807-0 2009 Antitumor activity of the selective MDM2 antagonist nutlin-3 against chemoresistant neuroblastoma with wild-type p53. nutlin 52-58 transformation related protein 53, pseudogene Mus musculus 113-116 19723889-7 2009 miR-16 was also shown to augment apoptosis induction by nutlin, a mouse double minute 2 (MDM2) antagonist, and genistein, a tyrosine kinase inhibitor, when added to a B-1 cell line derived from multiple in vivo passages of malignant B-1 cells from New Zealand Black mice with CLL. nutlin 56-62 microRNA 16-1 Mus musculus 0-6 20850924-1 2010 This study demonstrated a pronounced synergistic growth-inhibitory effect of an MDM2 inhibitor Nutlin-3 and a proteasome inhibitor bortezomib in mantle cell lymphoma (MCL) cells regardless of TP53 mutant status and innate bortezomib sensitivity. nutlin 95-101 MDM2 proto-oncogene Homo sapiens 80-84 21062913-0 2010 RITA inhibits multiple myeloma cell growth through induction of p53-mediated caspase-dependent apoptosis and synergistically enhances nutlin-induced cytotoxic responses. nutlin 134-140 zinc finger protein 331 Homo sapiens 0-4 19737973-7 2009 Retinoblastoma family members (pRb, p107, and p130) previously implicated in gene silencing during fibroblasts senescence were found down-regulated in cells with nutlin-induced senescence-like phenotype, suggesting a mechanism for its reversibility. nutlin 162-168 RB transcriptional corepressor like 1 Homo sapiens 36-40 19723889-7 2009 miR-16 was also shown to augment apoptosis induction by nutlin, a mouse double minute 2 (MDM2) antagonist, and genistein, a tyrosine kinase inhibitor, when added to a B-1 cell line derived from multiple in vivo passages of malignant B-1 cells from New Zealand Black mice with CLL. nutlin 56-62 transformed mouse 3T3 cell double minute 2 Mus musculus 89-93 19737973-7 2009 Retinoblastoma family members (pRb, p107, and p130) previously implicated in gene silencing during fibroblasts senescence were found down-regulated in cells with nutlin-induced senescence-like phenotype, suggesting a mechanism for its reversibility. nutlin 162-168 RB transcriptional corepressor like 2 Homo sapiens 46-50 19509161-12 2009 A combination of vincristine or actinomycin D with nutlin-3 enhanced the antitumor activity in RMS cell lines with wild-type p53. nutlin 51-57 tumor protein p53 Homo sapiens 125-128 19190243-4 2009 Of note, Nutlin-3 up-regulated Notch1 expression also in primary TP53(wild-type) B-chronic lymphocytic leukemia (B-CLL) cells and the combined use of Nutlin-3 plus pharmacological gamma-secretase inhibitors of the Notch signaling showed a synergistic cytotoxicity in both TP53(wild-type) leukemic cell lines and primary B-CLL cells. nutlin 9-15 notch receptor 1 Homo sapiens 31-37 19190243-4 2009 Of note, Nutlin-3 up-regulated Notch1 expression also in primary TP53(wild-type) B-chronic lymphocytic leukemia (B-CLL) cells and the combined use of Nutlin-3 plus pharmacological gamma-secretase inhibitors of the Notch signaling showed a synergistic cytotoxicity in both TP53(wild-type) leukemic cell lines and primary B-CLL cells. nutlin 9-15 tumor protein p53 Homo sapiens 65-69 19190243-4 2009 Of note, Nutlin-3 up-regulated Notch1 expression also in primary TP53(wild-type) B-chronic lymphocytic leukemia (B-CLL) cells and the combined use of Nutlin-3 plus pharmacological gamma-secretase inhibitors of the Notch signaling showed a synergistic cytotoxicity in both TP53(wild-type) leukemic cell lines and primary B-CLL cells. nutlin 9-15 notch receptor 1 Homo sapiens 31-36 19190243-4 2009 Of note, Nutlin-3 up-regulated Notch1 expression also in primary TP53(wild-type) B-chronic lymphocytic leukemia (B-CLL) cells and the combined use of Nutlin-3 plus pharmacological gamma-secretase inhibitors of the Notch signaling showed a synergistic cytotoxicity in both TP53(wild-type) leukemic cell lines and primary B-CLL cells. nutlin 9-15 tumor protein p53 Homo sapiens 272-276 16505116-12 2006 Our data suggest that nutlin is an effective radiosensitizer of p53 wild-type cells. nutlin 22-28 transformation related protein 53, pseudogene Mus musculus 64-67 19411846-10 2009 Surprisingly, blocking the transcriptional arm of p53, either via alpha-Amanitin or the p53-specific transcriptional inhibitor Pifithrin alpha, not only fails to inhibit, but greatly potentiates Nutlin-induced apoptosis. nutlin 195-201 tumor protein p53 Homo sapiens 50-53 19411846-10 2009 Surprisingly, blocking the transcriptional arm of p53, either via alpha-Amanitin or the p53-specific transcriptional inhibitor Pifithrin alpha, not only fails to inhibit, but greatly potentiates Nutlin-induced apoptosis. nutlin 195-201 tumor protein p53 Homo sapiens 88-91 16014563-8 2005 Mechanistic studies suggested that Nutlin-induced apoptosis was mediated by both transcriptional activation of proapoptotic Bcl-2 family proteins, and transcription-independent mitochondrial permeabilization resulting from mitochondrial p53 translocation. nutlin 35-41 transformation related protein 53 Mus musculus 237-240