RETRACTED: MicroRNA-141 inhibits glioma cells growth and metastasis by targeting TGF-β2 (Retracted article. See vol. 13, pg. 13225, 2021)

被引:2
作者
Peng, Tao [1 ]
Zhang, Shuyan [1 ]
Li, Wenchen [1 ]
Fu, Shuanglin [1 ]
Luan, Yongxin [1 ]
Zuo, Ling [2 ]
机构
[1] Jilin Univ, Hosp 1, Dept Neurosurg, Changchun 130021, Jilin Province, Peoples R China
[2] Jilin Univ, Hosp 2, Dept Ophthalmol, Changchun 130041, Jilin Province, Peoples R China
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2016年 / 8卷 / 08期
关键词
Glioma; miR-141; TGF-beta; 2; proliferation; migration; invasion; CANCER CELLS; MIR-141; PROLIFERATION; SUPPRESSOR; EXPRESSION; PATHWAY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNA-141 (miR-141) has been reported to function as tumor suppressor in many types of cancer. However, the molecular function and underlying mechanisms of miR-141 in glioma is still unknown. The aims of this study were to investigate miR-141 expression and determine its biological function and underlying mechanism in glioma. In this study, we found that miR-141 expression levels, both in glioma cell lines and in tissues, were significantly lower than that in a normal human astrocyte cell line or adjacent non-cancerous tissues. Overexpression of miR-141 significantly inhibited glioma cell proliferation, colony formation, migration and invasion in vitro, as well as suppressed glioma tumor growth in vivo. In addition, transforming growth factor beta 2 (TGF-beta 2) was identified as a target of miR-141 in glioma cells. TGF-beta 2 expression was also found to be upregulated, and negatively associated with miR-141 in glioma tissues. TGF-beta 2 over-expression partly reversed the effect caused by transfection of miR-141 mimic. These findings together suggested that miR-141 functioned as tumor suppressor by targeting TGF-V2, and that miR-141 might be a promising therapeutic strategy for future treatment of glioma.
引用
收藏
页码:3513 / 3521
页数:9
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