MicroRNA-940 inhibits epithelial-mesenchymal transition of glioma cells via targeting ZEB2

被引:0
|
作者
Xu, Ran [1 ]
Zhou, Fengqi [1 ]
Yu, Tianfu [1 ]
Xu, Guanhua [1 ]
Zhang, Junxia [1 ]
Wang, Yingyi [1 ]
Zhao, Lin [1 ]
Liu, Ning [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Neurosurg, Guangzhou Rd 300, Nanjing 210029, Jiangsu, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
miR-940; ZEB2; invasion/migration; EMT; glioma; TRANSCRIPTIONAL ACTIVATION; MOLECULAR PATHOLOGY; MIR-940; PROLIFERATION; GLIOBLASTOMA; EMT; PROGRESSION; MIGRATION; INVASION; GROWTH;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs have been found ectopically expressed in many cancers and play essential roles in tumor EMT progress. Recent studies identified decreased miR-940 expression in glioma cells and may serve as a tumor-suppressor. However, whether miR-940 involve in glioma EMT remain poorly understood. Here we confirmed that miR-940 was significantly reduced in glioma cells and tissues. Introduction of miR-940 dramatically suppressed invasion and migration of glioma cells. Gain-of-function experiments showed ZEB2 as a direct target of miR-940, knockdown of ZEB2 evidently repressed invasive capacity of glioma cells through EMT. Moreover, reintroduction of ZEB2 effectively reversed the tumor suppressive effect of miR-940 treatment. In vivo study showed reduced tumor cell motion in miR-940-injected groups. Spearman's correlation analysis indicated inversely correlated expression of ZEB2 and miR-940 in gliomas and NBTs. Altogether, miR-940-ZEB2 cascade may play important roles in glioma cells invasion and EMT progression, and might provide new therapeutic approaches for better outcomes of GBM patients.
引用
收藏
页码:7351 / 7363
页数:13
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