MiR-30a-5p is induced by Wnt/β-catenin pathway and promotes glioma cell invasion by repressing NCAM

被引:45
作者
Wang, Zhongyong [1 ]
Dai, Xingliang [1 ]
Chen, Yanming [1 ]
Sun, Chao [1 ]
Zhu, Qing [1 ]
Zhao, Haifeng [2 ]
Liu, Guodong [1 ]
Huang, Qiang [1 ]
Lan, Qing [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 2, Dept Neurosurg, Suzhou 215004, Peoples R China
[2] Soochow Univ, Affiliated Hosp 2, Dept Pathol, Suzhou 215004, Peoples R China
基金
中国国家自然科学基金;
关键词
Wnt/beta-catenin; MiR-30a-5p; NCAM; Cell invasion; ADHESION MOLECULE; MICRORNA EXPRESSION; WNT; CARCINOMA; CD56;
D O I
10.1016/j.bbrc.2015.08.007
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
Wnt/beta-catenin signaling pathway is frequently dysregulated in human tumors and plays a critical role in tumorigenesis; however, the roles of microRNAs in mediating Wnt/b-catenin pathway are not well understood. Herein, we show that miR-30a-5p is activated by Wnt/beta-catenin pathway through direct binding of beta-catenin/TCF4 to two sites in the promoter region of miR-30a-5p. We also found that miR-30a-5p represses neural cell adhesion molecule (NCAM) expression by directly targeting two sites in the 3' untranslated region (3'-UTR) of NCAM mRNA. Moreover, Wnt/beta-catenin pathway represses NCAM expression in glioma cells, which depends on miR-30a-5p. Finally, we found that miR-30a-5p promotes glioma cell growth invasion by repressing NCAM. Our findings demonstrate a novel Wnt/beta-catenin-miR-30a-5p NCAM regulatory axis which plays important roles in controlling glioma cell invasion and tumorigenesis. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:374 / 380
页数:7
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