异位表达
胶质瘤
癌症研究
小RNA
体内
抑制器
癌症
细胞凋亡
细胞生长
生物
U87型
细胞培养
体外
基因
生物技术
遗传学
生物化学
作者
Yongmei Jiang,Lian Yin,Huirong Jing,Hui Zhang
出处
期刊:Tumor Biology
[SAGE]
日期:2015-06-17
卷期号:36 (11): 8943-8951
被引量:26
标识
DOI:10.1007/s13277-015-3651-4
摘要
Previous studies have shown that miR-219-5p is dysregulated and exerts tumor-suppressive effects in cancer development and progression. However, the molecular function and mechanism of miR-219-5p in glioblastoma growth and invasion are still unclear. In the present study, we show that miR-219-5p was downregulated in a panel of glioma tissues with different grades and in all the human glioma cell lines examined. Ectopic expression of miR-219-5p inhibited proliferation and invasion and induced apoptosis in vitro, and xenograft formation in vivo. ROBO1 was found to be a direct target of miR-219-5p, and when overexpressed in miR-219-5p-expressing glioma cells, was able to restore proliferative and invasive ability. Finally, in vivo investigation confirmed that miR-219-5p was a tumor suppressor that regulated ROBO1 expression. Taken together, these studies demonstrate that miR-219-5p inhibited cancer cell growth and invasion by direct targeting ROBO1, implicating miR-219-5p as an attractive candidate for cancer therapy.
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