microRNA-200a is an independent prognostic factor of hepatocellular carcinoma and induces cell cycle arrest by targeting CDK6

被引:38
|
作者
Xiao, Fenqiang [1 ]
Zhang, Wu [2 ]
Zhou, Lin [1 ]
Xie, Haiyang [1 ]
Xing, Chunyang [1 ]
Ding, Songming [1 ]
Chen, Kangjie [2 ]
Zheng, Shusen [1 ,2 ]
机构
[1] Minist Publ Hlth, Key Lab Organ Transplantat, Key Lab Combined Multiorgan Transplantat, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Div Hepatobiliary & Pancreat Surg, Hangzhou 310000, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
hepatocellular carcinoma; microRNA-200a; CDK6; overall survival; cell cycle arrest; SUPPRESSES TUMORIGENICITY; HUMAN CANCERS; EXPRESSION; TRANSITION; SIGNATURES; PROFILES; FAMILY;
D O I
10.3892/or.2013.2715
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Deregulation of microRNA-200a (miR-200a) has been observed in different types of diseases, including cancers. However, the exact roles of miR-200a in hepatocellular carcinoma (HCC) are still largely unknown. We aimed to elucidate the prognostic implications of miR-200a and its biological function in HCC. Quantitative polymerase chain reaction was used to evaluate miR-200a expression. Western blotting was performed to evaluate the protein level. Gain-of-function studies were performed to evaluate the roles of miR-200a in HCC. Our results revealed that miR-200a was frequently downregulated in HCC. In addition, multivariate analysis confirmed that miR-200a was significantly associated with the overall survival of HCC patients. In vitro assays demonstrated that miR-200a suppressed the proliferation of HCC cells by induction of G1 phase arrest. Furthermore, CDK6 was identified as a novel functional target of miR-200a. Our data indicate that miR-200a functions as a potential tumor suppressor in HCC.
引用
收藏
页码:2203 / 2210
页数:8
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