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

被引:33
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
相关论文
共 36 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[3]   miR-27b-3p inhibits proliferation and potentially reverses multi-chemoresistance by targeting CBLB/GRB2 in breast cancer cells [J].
Chen, Danni ;
Si, Wengong ;
Shen, Jiaying ;
Du, Chengyong ;
Lou, Weiyang ;
Bao, Chang ;
Zheng, Huilin ;
Pan, Jie ;
Zhong, Guansheng ;
Xu, Liang ;
Fu, Peifen ;
Fan, Weimin .
CELL DEATH & DISEASE, 2018, 9
[4]   miR-143 acts as a novel Big mitogen-activated protein kinase 1 suppressor and may inhibit invasion of glioma [J].
Chen, Wei-Yi ;
Lang, Zhi-Qiang ;
Ren, Chao ;
Yang, Ping ;
Zhang, Baogang .
ONCOLOGY REPORTS, 2019, 42 (03) :1194-1204
[5]   Noncoding RNAs: New Players in Cancers [J].
Chen, Xueman ;
Fan, Siting ;
Song, Erwei .
LONG AND SHORT NONCODING RNAS IN CANCER BIOLOGY, 2016, 927 :1-47
[6]   Long non-coding RNA HCG11 modulates glioma progression through cooperating with miR-496/CPEB3 axis [J].
Chen, Yangzong ;
Bao, Chunchun ;
Zhang, Xiuxing ;
Lin, Xinshi ;
Huang, Hongou ;
Wang, Zhiqiang .
CELL PROLIFERATION, 2019, 52 (05)
[7]  
Chen Y, 2019, AM J TRANSL RES, V11, P5988
[8]   Molecular architecture of a miRNA-regulated 3′ UTR [J].
Didiano, Dominic ;
Hobert, Oliver .
RNA, 2008, 14 (07) :1297-1317
[9]   Consensus on the role of human cytomegalovirus in glioblastoma [J].
Dziurzynski, Kristine ;
Chang, Susan M. ;
Heimberger, Amy B. ;
Kalejta, Robert F. ;
Dallas, Stuart R. McGregor ;
Smit, Martine ;
Soroceanu, Liliana ;
Cobbs, Charles S. .
NEURO-ONCOLOGY, 2012, 14 (03) :246-255
[10]   Animal viruses, bacteria, and cancer: a brief commentary [J].
Efird, JimmyT. ;
Davies, Stephen W. ;
O'Neal, Wesley T. ;
Anderson, Ethan J. .
FRONTIERS IN PUBLIC HEALTH, 2014, 2