| Literature DB >> 26669804 |
Jizhong Ren1, Xiuwu Pan1,2, Lin Li1,2, Yi Huang1, Hai Huang1, Yi Gao1, Hong Xu1, Fajun Qu1, Lu Chen1, Linhui Wang1, Yi Hong1, Xingang Cui2, Danfeng Xu3.
Abstract
GPR137 belongs to the G protein-coupled receptor family involving the regulation of transmembrane signal transduction that launches pivotal cellular functions. However, its function in prostate cancer (PCa) has been rarely reported. It was found in this study that GPR137 was upregulated in PCa tissues as compared with that in paracancerous tissues. To see whether GPR137 could serve as a potential therapeutic target for PCa, GPR137 was knocked down to verify its biological function in PCa cells. Lentivirus-introduced short hairpin RNA (shRNA) was designed to silence GPR137 gene. It was found that silencing of GPR137 gene suppressed the proliferation and colony formation of PCa cell lines PC-3 and DU145. Further study indicated that growth inhibition by GPR137 knockdown was associated with cell cycle arrest at G0/G1 phase. Furthermore, silencing of GPR137 repressed the invasion and migration abilities of PC-3 cells via downregulating slug and snail and upregulating E-cadherin. Collectively, these findings imply that GPR137 plays an important role in the occurrence and progression of PCa and may prove to be a potential therapeutic target for the treatment of advanced PCa.Entities:
Keywords: GPR137; migration; proliferation; prostate cancer
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Year: 2016 PMID: 26669804 DOI: 10.1111/cbdd.12704
Source DB: PubMed Journal: Chem Biol Drug Des ISSN: 1747-0277 Impact factor: 2.817