PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 26220174-2 2015 This metabolic switch activates mechanistic target of rapamycin complex 1 (mTORC1), which initiates growth by increasing protein and RNA synthesis and fatty acid metabolism, while decreasing autophagy. Fatty Acids 151-161 CREB regulated transcription coactivator 1 Mus musculus 75-81 34685712-0 2021 Activation of mTORC1 by Free Fatty Acids Suppresses LAMP2 and Autophagy Function via ER Stress in Alcohol-Related Liver Disease. Fatty Acids 29-40 CREB regulated transcription coactivator 1 Mus musculus 14-20 34267188-8 2021 The pathological effect of sustained mTORC1 activity in ALD may be attributed to the suppression of peroxisome proliferator activated receptor alpha (PPARalpha), the master regulator of fatty acid oxidation in hepatocytes, because fenofibrate (PPARalpha agonist) treatment reverses ethanol-induced liver steatosis and inflammation in Depdc5-LKO mice. Fatty Acids 186-196 CREB regulated transcription coactivator 1 Mus musculus 37-43 34146544-6 2021 Further, we examined whether the activation of the anabolic program mediated by mTORC1 complex activation in the fasted state could suppress the robust catabolic programming and enhanced PPARalpha transcriptional response of mice with a liver-specific defect in mitochondrial long-chain fatty acid oxidation using Cpt2L-/- mice. Fatty Acids 287-297 CREB regulated transcription coactivator 1 Mus musculus 80-86 33401933-14 2021 Conclusions: TSC2-S1365 phosphorylation status regulates myocardial substrate utilization, and its decline activates mTORC1 biasing metabolism away from fatty acid oxidation to glycolysis to confer protection against IR. Fatty Acids 153-163 CREB regulated transcription coactivator 1 Mus musculus 117-123 33303821-0 2020 Saturated fatty acids induce insulin resistance in podocytes through inhibition of IRS1 via activation of both IKKbeta and mTORC1. Fatty Acids 0-21 CREB regulated transcription coactivator 1 Mus musculus 123-129 31673045-10 2019 In addition, the activation of mTORC1 by SCD1 deficiency reveals an important function of fatty acids in regulating different cellular processes through mTORC1 signaling. Fatty Acids 90-101 CREB regulated transcription coactivator 1 Mus musculus 31-37 33219129-7 2021 Interestingly, ABHD5-dependent suppression of mTORC1 was abrogated by pharmacological inhibition of DGAT1 or DGAT2, isoenzymes that re-esterify fatty acids in a process that consumes ATP. Fatty Acids 144-155 CREB regulated transcription coactivator 1 Mus musculus 46-52 31394165-5 2019 The investigation of molecular mechanisms responsible for the sexual dimorphisms delineated the selective activation of the ERK/mTORc1 signaling pathway leading to an increased biosynthesis and elongation of fatty acids in VLCAD-/- females. Fatty Acids 208-219 CREB regulated transcription coactivator 1 Mus musculus 128-134 31673045-10 2019 In addition, the activation of mTORC1 by SCD1 deficiency reveals an important function of fatty acids in regulating different cellular processes through mTORC1 signaling. Fatty Acids 90-101 CREB regulated transcription coactivator 1 Mus musculus 153-159 29457836-8 2018 DEPTOR-dependent inhibition of mTORC1 also attenuated alcohol-induced cytoplasmic accumulation of the lipogenic regulator lipin 1 and prevented alcohol-mediated inhibition of fatty acid oxidation. Fatty Acids 175-185 CREB regulated transcription coactivator 1 Mus musculus 31-37 31338091-5 2019 These enhanced TORC1 pathway activities may culminate in increased expression of the nuclear receptor peroxisome proliferator-activated receptor gamma (Ppargamma) that regulates fatty acid storage, and the transcription factor sterol regulatory element-binding transcription factor 1 (Srebf1). Fatty Acids 178-188 CREB regulated transcription coactivator 1 Mus musculus 15-20 30909319-7 2019 Decreased mTORC1 activity in turn mediates an elevation of fatty acid oxidation (FAO) by indirectly upregulating the expression of carnitine palmitoyltransferase 1a (Cpt1a) that mediates the rate-limiting step of beta-oxidation. Fatty Acids 59-69 CREB regulated transcription coactivator 1 Mus musculus 10-16 30298052-7 2018 Here, we show that under the physiological condition of acute lipogenesis, lobeglitazone inhibits hepatic lipid synthesis, the subsequent ER stress, and omega-oxidation of fatty acids by inhibiting the mTORC1 pathway. Fatty Acids 172-183 CREB regulated transcription coactivator 1 Mus musculus 202-208 27901044-3 2016 Here, we show that the mTORC1-PPARgamma pathway is crucial for the fatty acid uptake programme in activated CD4+ T cells. Fatty Acids 67-77 CREB regulated transcription coactivator 1 Mus musculus 23-29 28223357-3 2017 We report here that mTORC1 and mTORC2 are activated in response to exogenously supplied fatty acids via the de novo synthesis of PA, a central metabolite for membrane phospholipid biosynthesis. Fatty Acids 88-99 CREB regulated transcription coactivator 1 Mus musculus 20-26 26204830-0 2015 Inhibition of Mammalian Target of Rapamycin Complex 1 (mTORC1) Downregulates ELOVL1 Gene Expression and Fatty Acid Synthesis in Goat Fetal Fibroblasts. Fatty Acids 104-114 CREB regulated transcription coactivator 1 Mus musculus 55-61 26204830-2 2015 Mammalian target of rapamycin complex 1 (mTORC1) is a central regulator of cell metabolism and is associated with fatty acids synthesis. Fatty Acids 114-125 CREB regulated transcription coactivator 1 Mus musculus 41-47 26204830-5 2015 Inhibition of mTORC1 by rapamycin decreased ELOVL1 expression and fatty acids synthesis in Cashmere goat fetal fibroblasts. Fatty Acids 66-77 CREB regulated transcription coactivator 1 Mus musculus 14-20 26204830-6 2015 These data show that ELOVL1 expression is regulated by mTORC1 and that mTORC1 has significant function in fatty acids synthesis in Cashmere goat. Fatty Acids 106-117 CREB regulated transcription coactivator 1 Mus musculus 71-77 25985629-3 2015 mTOR complex 1 (mTORC1) controls multiple cellular processes, including protein synthesis, glucose metabolism, fatty acid and sterol synthesis, mitochondrial biogenesis, and autophagy. Fatty Acids 111-121 CREB regulated transcription coactivator 1 Mus musculus 16-22 26112996-7 2015 CONCLUSION: High levels of AAs up-regulate hepatic fatty acid biosynthetic gene expression through an mTORC1-dependent manner, while attenuate insulin-mediated repression of gluconeogenesis through elevating IRS-1 Ser(302) phosphorylation, which in turn impairs Akt activation and thereby weakening insulin action. Fatty Acids 51-61 CREB regulated transcription coactivator 1 Mus musculus 102-108 22877732-4 2012 More particularly, it aims at providing an overview of the status of knowledge regarding the mechanisms underlying the ability of certain amino acids, glucose and fatty acids, to affect mTORC1 activity and in turn illustrates how the mTORC1 pathway couples nutrient sensing to the hypothalamic regulation of the organisms" energy homoeostasis and to the control of intracellular metabolic processes, such as glucose uptake, protein and lipid biosynthesis. Fatty Acids 163-174 CREB regulated transcription coactivator 1 Mus musculus 186-192 24726883-0 2014 Fatty acids are novel nutrient factors to regulate mTORC1 lysosomal localization and apoptosis in podocytes. Fatty Acids 0-11 CREB regulated transcription coactivator 1 Mus musculus 51-57 22877732-4 2012 More particularly, it aims at providing an overview of the status of knowledge regarding the mechanisms underlying the ability of certain amino acids, glucose and fatty acids, to affect mTORC1 activity and in turn illustrates how the mTORC1 pathway couples nutrient sensing to the hypothalamic regulation of the organisms" energy homoeostasis and to the control of intracellular metabolic processes, such as glucose uptake, protein and lipid biosynthesis. Fatty Acids 163-174 CREB regulated transcription coactivator 1 Mus musculus 234-240 19305497-0 2009 Glucose amplifies fatty acid-induced endoplasmic reticulum stress in pancreatic beta-cells via activation of mTORC1. Fatty Acids 18-28 CREB regulated transcription coactivator 1 Mus musculus 109-115 19305497-14 2009 Moreover, in stressed beta-cells mTORC1 inhibition decreases IRE1alpha protein expression and JNK activity without affecting ER protein load, suggesting that mTORC1 regulates the beta-cell stress response to glucose and fatty acids by modulating the synthesis and activity of specific proteins involved in the execution of the ER stress response. Fatty Acids 220-231 CREB regulated transcription coactivator 1 Mus musculus 33-39 19305497-14 2009 Moreover, in stressed beta-cells mTORC1 inhibition decreases IRE1alpha protein expression and JNK activity without affecting ER protein load, suggesting that mTORC1 regulates the beta-cell stress response to glucose and fatty acids by modulating the synthesis and activity of specific proteins involved in the execution of the ER stress response. Fatty Acids 220-231 CREB regulated transcription coactivator 1 Mus musculus 158-164