细胞生长
细胞周期
基因敲除
RNA干扰
G蛋白偶联受体
细胞
细胞生物学
信号转导
细胞培养
生物
流式细胞术
细胞凋亡
癌症研究
受体
分子生物学
核糖核酸
遗传学
基因
作者
Xin Shao,Yong Liu,Hai Huang,Linyuan Zhuang,Tianping Luo,Huping Huang,GE Xin-guo
摘要
G protein-coupled receptors (GPCRs) are important signal transduction mediators and pharmacological therapeutic targets. G protein-coupled receptor 137 (GPR137) was initially reported as a novel orphan GPCR around 10 years ago. Some orphan GPCRs have been implicated in cancer cell proliferation and migration. The aim of this study is to investigate the role of GPR137 in hepatocellular carcinoma (HCC). GPR137 is widely expressed in several human HCC cell lines, as determined by real-time PCR. We then applied lentivirus mediated RNA interference (RNAi) to knock down GPR137 expression in two HCC cell lines HepG2 and Bel7404. Depletion of GPR137 remarkably inhibited cell proliferation and colony formation capacity. Knockdown of GPR137 in HepG2 cells led to cell cycle arrest at G0/G1 phase and G2/M phase, and induced cell apoptosis, as determined by flow cytometry analysis, which contributed to cell growth inhibition. Our findings suggested that GPR137 could facilitate HCC cell proliferation and thus promote hepatocarcinogenesis.
科研通智能强力驱动
Strongly Powered by AbleSci AI