Wang Zishu, Zhang Hui, Wang Junbin, Yang Yan, Wu Qiong
Department of Medical Oncology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui 233004, P.R. China.
Department of Surgery Oncology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui 233004, P.R. China.
Mol Med Rep. 2015 Apr;11(4):2578-84. doi: 10.3892/mmr.2014.3091. Epub 2014 Dec 15.
G protein‑coupled receptor 137 (GPR137) is an integral membrane protein, which belongs to the GPR137 family of cell surface mediators of signal transduction. GPF137 was recently identified; however, its role in human disease onset has remained to be elucidated. GPR137 is highly expressed in multiple human gastric cancer cell lines. A GPR137 short hairpin RNA (shRNA)‑expressing vector was transfected into AGS and MGC80‑3 gastric cancer cells, and the subsequent depletion of GPR137 resulted in a significant reduction in cell proliferation and colony formation, as determined by MTT and colony formation assays. In addition, cell cycle analysis indicated that GPR137 knockdown arrested MGC80‑3 cells in G2/M phase. To the best of our knowledge, the present study was the first to investigate the role of GPR137 in gastric tumorigenesis and revealed that knockdown of GPR137 by lentivirus‑mediated shRNA transfection inhibited the growth of gastric cancer cells in vitro. These results indicated that GPR137 may present a novel target for the development of pharmacological therapeutics for human gastric cancer.
G蛋白偶联受体137(GPR137)是一种整合膜蛋白,属于信号转导的细胞表面介质GPR137家族。GPR137最近才被发现;然而,其在人类疾病发病中的作用仍有待阐明。GPR137在多种人类胃癌细胞系中高表达。将表达GPR137短发夹RNA(shRNA)的载体转染到AGS和MGC80-3胃癌细胞中,随后GPR137的缺失导致细胞增殖和集落形成显著减少,这通过MTT和集落形成试验确定。此外,细胞周期分析表明,GPR137基因敲低使MGC80-3细胞停滞在G2/M期。据我们所知,本研究首次探讨了GPR137在胃癌发生中的作用,并揭示通过慢病毒介导的shRNA转染敲低GPR137可在体外抑制胃癌细胞的生长。这些结果表明,GPR137可能是人类胃癌药物治疗开发的一个新靶点。