The G-protein-coupled bile acid receptor Gpbar1 (TGR5) suppresses gastric cancer cell proliferation and migration through antagonizing STAT3 signaling pathway

التفاصيل البيبلوغرافية
العنوان: The G-protein-coupled bile acid receptor Gpbar1 (TGR5) suppresses gastric cancer cell proliferation and migration through antagonizing STAT3 signaling pathway
المؤلفون: Cong Guo, Rui Xiao, Yan-Dong Wang, Meng Zhang, Donna Yu, Jianxun Wen, Jia Su, Zhijun Li, Wendong Huang, Xueting Zhang, Yanyan Li, Wei-Dong Chen
المصدر: Oncotarget
بيانات النشر: Impact Journals, LLC, 2015.
سنة النشر: 2015
مصطلحات موضوعية: STAT3 Transcription Factor, Immunoblotting, Gpbar1, Apoptosis, Real-Time Polymerase Chain Reaction, Transfection, Stat3 Signaling Pathway, Receptors, G-Protein-Coupled, STAT3, Cell Movement, Stomach Neoplasms, Cell Line, Tumor, Humans, Cell Proliferation, biology, Cell growth, gastric cancer, TGR5, Flow Cytometry, G protein-coupled bile acid receptor, bile acid receptor, Oncology, Cancer cell, Cancer research, biology.protein, Phosphorylation, Signal transduction, Signal Transduction, Research Paper
الوصف: Gpbar1 (TGR5), a membrane-bound bile acid receptor, is well known for its roles in regulation of energy homeostasis and glucose metabolism. Here we show that TGR5 is a suppressor of gastric cancer cell proliferation and migration through antagonizing STAT3 signaling pathway. We firstly show that TGR5 activation greatly inhibited proliferation and migration of human gastric cancer cells and strongly induced gastric cancer cell apoptosis. We then found that TGR5 activation antagonized STAT3 signaling pathway through suppressing the phosphorylation of STAT3 and its transcription activity induced by lipopolysaccharide (LPS) or interleukin-6. TGR5 overexpression with ligand treatment inhibited gene expression mediated by STAT3. It suggests that TGR5 antagonizes gastric cancer proliferation and migration at least in part by inhibiting STAT3 signaling. These findings identify TGR5 as a suppressor of gastric cancer cell proliferation and migration that may serve as an attractive therapeutic tool for human gastric cancer.
تدمد: 1949-2553
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::025fe4bbd301cc9930d8dc6f71850904
https://doi.org/10.18632/oncotarget.5353
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....025fe4bbd301cc9930d8dc6f71850904
قاعدة البيانات: OpenAIRE