MiR-27b-3p suppresses glioma development via targeting YAP1

被引:26
|
作者
Miao, Wei [1 ]
Li, Ning [1 ]
Gu, Bin [1 ]
Yi, Guoqing [1 ]
Su, Zheng [1 ]
Cheng, Huilin [1 ]
机构
[1] Southeast Univ, Zhongda Hosp, Dept Neurosurg, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-27b-3p; glioma; YAP1; microRNA; CANCER-CELLS; PROLIFERATION; METASTASIS; MIGRATION; INVASION; PROMOTES;
D O I
10.1139/bcb-2019-0300
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
Previous studies have reported that miRNAs are involved in the progression of glioma, and that miR-27b-3p is involved in a variety of cancers. However, whether miR-27b-3p has a role in glioma is still unknown. Here, we demonstrated that miR-27b-3p is downregulated in glioma, and this is associated with the development of glioma. Overexpression of miR-27b-3p in glioma cells inhibits cell proliferation and migration, and induces cell apoptosis, which suppresses the progression of glioma Furthermore, in our study, overexpression of miR-27b-3p also inhibited the growth of xenografted glioma tumors in-vivo. Finally, we verified that Yes Associated Protein 1 (YAP1) is the downstream target of miR-27b-3p, and that miR-27b-3p controls the proliferation, migration, and apoptosis of glioma cells via regulating YAP1. Our study reveals a novel mechanism through which miR-27b-3p functions in the development of glioma, and thus provides a potential therapeutic target for the treatment of glioma.
引用
收藏
页码:466 / 473
页数:8
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