MiR-124 inhibits cell proliferation, invasion, and migration in glioma by targeting Smad2

被引:1
作者
Lv, Zhonghua [1 ]
Zhao, Yashuang [2 ]
机构
[1] Harbin Med Univ, Heilongjiang Inst Canc Res, Affiliated Hosp 3, Dept Neurosurg, Harbin, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Sch Publ Hlth, 157 Baojian St, Harbin 150081, Heilongjiang, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2017年 / 10卷 / 11期
关键词
MiR-124; glioma; Smad2; migration; invasion; TGF-BETA; CANCER; EXPRESSION; MICRORNAS; PROTEINS; IDENTIFICATION; PATHWAY; MOUSE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumorigenesis research has focused on the roles of deregulated microRNAs for many years. The aberrant expression of miR-124 in many tumors has been widely reported, yet its role in glioma formation still needs further research. In this study, the expression and mechanisms of miR-124 in glioma development were explored. We found that glioma cell lines and tumor tissues demonstrated downregulated miR-124 expression, and that cell proliferation, migration, and invasion were reduced when miR-124 was restored. Furthermore, a bioinformatic analysis indicated that Smad2 was a putative target of miR-124, and we confirmed that miR-124 directly targets Smad2 in a luciferase reporter assay system. These results indicate that glioma cell growth is suppressed by miR-124 through its negative regulation of Smad2 expression. Our findings disclose a critical role of miR-124 in glioma pathogenesis, and suggest its potential application for glioma therapy.
引用
收藏
页码:11369 / 11376
页数:8
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