CFTR activation suppresses glioblastoma cell proliferation, migration and invasion

被引:14
作者
Zhong, Xiao [1 ]
Chen, Hong-qi [2 ]
Yang, Xiu-ling [1 ]
Wang, Qing [1 ]
Chen, Wenliang [2 ]
Li, Chunfu [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Paediat, Guangzhou, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Dept Pharmacol, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
CFTR; Glioblastoma; Proliferation; Migration; Invasion; TRANSMEMBRANE CONDUCTANCE REGULATOR; CYSTIC-FIBROSIS; DOWN-REGULATION; DIFFERENTIATION; TEMOZOLOMIDE; INHIBITION;
D O I
10.1016/j.bbrc.2018.12.080
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
The aim of this study was to investigate the function of Cystic fibrosis transmembrane conductance regulator (CFTR) in human glioblastoma (GBM) cells. Data dining results of the Human Protein Atlas showed that low CFTR expression was associated with poor prognosis for GBM patients. We found that CFTR protein expression was lower in U87 and U251 GBM cells than that in normal humane astrocyte cells. CFTR activation significantly reduced GBM cell proliferation. In addition, CFTR activation significantly abrogated migration and invasion of GBM cells. Besides, CFTR activator Forskolin treatment markedly reduced MMP-2 protein expression. These effects of CFTR activation were significantly inhibited by CFTR inhibitor CFTRinh-172 pretreatment. Our findings suggested that JAK2/STAT3 signaling was involved in the anti-glioblastoma effects of CFTR activation. Moreover, CFTR overexpression in combination with Forskolin induced a synergistic anti-proliferative response in U87 cells. Overall, our findings demonstrated that CFTR activation suppressed GBM cell proliferation, migration and invasion likely through the inhibition of JAK2/STAT3 signaling. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:1279 / 1285
页数:7
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