岩石1
癌症研究
细胞生长
肝细胞癌
细胞凋亡
生物
细胞周期
激酶
蛋白激酶A
细胞周期检查点
细胞
细胞生物学
生物化学
作者
Quanjun Deng,Li Xie,Hua Li
标识
DOI:10.1016/j.bbrc.2015.10.043
摘要
Recent studies have shown that miR-506 plays important roles in human cancer progression. However, little is known about the function of miR-506 in hepatocellular carcinoma (HCC). In this study, we found that miR-506 significantly inhibits HCC cell proliferation in vitro and tumorigenicity in vivo. Moreover, miR-506 induced G1/S cell cycle arrest and apoptosis in HCC cells. Rho-associated protein kinase 1(ROCK1) was identified as a novel target of miR-506; overexpression of ROCK1 reversed the suppressive effects of miR-506 in HCC cells. Additionally, ROCK1 was found up-regulated and inversely correlated with miR-506 in HCC tissues. Therefore, our findings collectively suggest that miR-506 acts as a tumor suppressor via regulation of ROCK1 expression and may thus be a promising therapeutic target for HCC.
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