MicroRNA-193b regulates proliferation, migration and invasion in human hepatocellular carcinoma cells

被引:135
作者
Xu, Chengwang [1 ]
Liu, Shanshan [1 ,2 ]
Fu, Hanjiang [1 ]
Li, Shuai [1 ]
Tie, Yi [1 ]
Zhu, Jie [1 ]
Xing, Ruiyun [1 ]
Jin, Yinghua [2 ]
Sun, Zhixian [1 ]
Zheng, Xiaofei [1 ]
机构
[1] Beijing Inst Radiat Med, Beijing 100850, Peoples R China
[2] Jilin Univ, Sch Life Sci, Changchun 130012, Jilin, Peoples R China
关键词
MicroRNA; Invasion; Migration; Cell cycle; DOWN-REGULATION; C-MET; EXPRESSION; CANCER; INVOLVEMENT; METASTASIS; TARGET; ETS-1; GENE;
D O I
10.1016/j.ejca.2010.06.127
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Aims: Recently, some miRNAs have been reported to be connected closely with the development of human hepatocellular carcinoma. However, the functions of these miRNAs in HCC remain largely undefined. Methods: The expression profiles of miR-193b were compared between HCC tissues and adjacent normal liver tissues using qRT-PCR method. This method was also be used to screen the potential target genes of miR-193b. A luciferase reporter assay was conducted to confirm target association. Finally, the functional effect of miR-193b in hepatoma cells was examined further. Results: miR-193b was significantly down-regulated in most of the HCC tissues compared to the matching non-tumoural liver tissues. Furthermore, ectopic expression of miR-193b dramatically suppressed the ability of hepatoma cells to form colonies in vitro and to develop tumours in nude mice. CCND1 and ETS1 were revealed to be regulated by miR-193b directly. By regulating the expressions of these oncogenes, miR-193b induced cell cycle arrest and inhibited the invasion and migration of hepatoma cells. Conclusions: miR-193b may function as a tumour suppressor in the development of HCC by acting on multiple tumourigenic pathways. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2828 / 2836
页数:9
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