MiR-126 suppresses colon cancer cell proliferation and invasion via inhibiting RhoA/ROCK signaling pathway

被引:52
作者
Li, Nan [1 ,2 ]
Tang, Anliu [1 ,2 ]
Huang, Shuo [1 ]
Li, Zeng [1 ]
Li, Xiayu [1 ,2 ]
Shen, Shourong [1 ,2 ]
Ma, Jian [2 ,3 ,4 ,5 ]
Wang, Xiaoyan [1 ,2 ]
机构
[1] Cent S Univ, Xiangya Hosp 3, Dept Gastroenterol, Changsha, Hunan, Peoples R China
[2] Hunan Key Lab Nonresolving Inflammat & Canc, Changsha, Hunan, Peoples R China
[3] Cent S Univ, Canc Res Inst, Changsha, Hunan, Peoples R China
[4] Minist Hlth, Key Lab Carcinogenesis, Changsha, Hunan, Peoples R China
[5] Minist Educ, Key Lab Carcinogenesis & Canc Invas, Changsha, Hunan, Peoples R China
关键词
MiR-126; Colon cancer; Cancer proliferation; Cancer metastasis; RhoA; RHO-GTPASES; BREAST-CANCER; COLORECTAL-CANCER; MICRORNA; EXPRESSION; METASTASIS; PROGNOSIS; CARCINOMA; MIGRATION; PROFILES;
D O I
10.1007/s11010-013-1664-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent data strongly suggests the profound role of miRNAs in cancer progression. Here, we showed miR-126 expression was much lower in HCT116, SW620 and HT-29 colon cancer cells with highly metastatic potential and miR-126 downregulation was more frequent in colorectal cancers with metastasis. Restored miR-126 expression inhibited HT-29 cell growth, cell-cycle progression and invasion. Mechanically, microarray results combined with bioinformatic and experimental analysis demonstrated miR-126 exerted cancer suppressor role via inhibiting RhoA/ROCK signaling pathway. These results suggest miR-126 function as a potential tumor suppressor in colon cancer progression and miR-126/RhoA/ROCK may be a novel candidate for developing rational therapeutic strategies.
引用
收藏
页码:107 / 119
页数:13
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