miR-125b Inhibits Connexin43 and Promotes Glioma Growth

被引:57
作者
Jin, Zheng
Xu, Songbai
Yu, Hongquan
Yang, Boyu
Zhao, Hongguang
Zhao, Gang
机构
[1] Department of Neurosurgery, First Hospital, Jilin University, Jilin
[2] Department of Radiology, First Hospital, Jilin University, Jilin
关键词
MicroRNA; Glioma; Connexin43; mRNA; GLIOBLASTOMA STEM-CELLS; RANDOMIZED PHASE-III; ADJUVANT TEMOZOLOMIDE; 5-YEAR ANALYSIS; PROLIFERATION; EXPRESSION; MICRORNAS; RADIOTHERAPY; CONCOMITANT; SURVIVAL;
D O I
10.1007/s10571-013-9980-1
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
MicroRNA is strongly associated with tumor growth and development. This study examined the potential roles of miR-125b in glioma growth. We found that miR-125b promotes glioma cell line growth and clone formation, and protects the glioma cells from apoptosis in vitro. The miR-125b-transfected glioma cells also demonstrated increased growth after in vivo transplantation. We further identified that miR-125b inhibits Connexin43 expression, and the overexpression of Connexin43 antagonizes the effects of miR-125b in cell growth and anti-apoptosis. We conclude that miR-125b regulates glioma growth partly through Connexin43 protein.
引用
收藏
页码:1143 / 1148
页数:6
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