MicroRNA-101 suppresses motility of bladder cancer cells by targeting c-Met

被引:57
|
作者
Hu, Zhenghui [1 ]
Lin, Yiwei [1 ]
Chen, Hong [1 ]
Mao, Yeqing [1 ]
Wu, Jian [1 ]
Zhu, Yi [1 ]
Xu, Xin [1 ]
Xu, Xianglai [1 ]
Li, Shiqi [1 ]
Zheng, Xiangyi [1 ]
Xie, Liping [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Urol, Hangzhou 310003, Zhejiang, Peoples R China
关键词
miR-101; c-Met; Bladder cancer; Migration; Invasion; UROTHELIAL CARCINOMA; GASTRIC-CANCER; MIGRATION; INVASION; EXPRESSION; MIR-101; GROWTH; PROLIFERATION; ACTIVATION; MECHANISM;
D O I
10.1016/j.bbrc.2013.04.042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are small non-coding RNAs that play regulatory roles by repressing translation or cleaving RNA transcripts. Here, we report that the expression of microRNA-101 (miR-101) is down-regulated in human bladder cancer tissue versus normal adjacent tissue. To better characterize the role of miR-101 in bladder cancer, we conducted a gain-of-function analysis by transfecting the bladder cancer cell line T24 with chemically synthesized miR-101 mimics. We found that miR-101 directly targets c-Met via its 3'-UTR. Specifically, forced expression of miR-101 decreased c-Met expression at both mRNA and protein levels, consequently inhibiting T24 cell migration and invasion in a c-Met-dependent manner. In conclusion, we have shown miR-101 to be a novel suppressor of T24 cell migration and invasion through its negative regulation of c-Met. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:82 / 87
页数:6
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