基因敲除
胶质瘤
转化生长因子
癌症研究
车站3
细胞生物学
磷酸化
化学
生物
细胞培养
遗传学
作者
Hongliang Wang,Feng Tang,Erbao Bian,Yile Zhang,Xinghu Ji,Zhihao Yang,Bing Zhao
标识
DOI:10.1007/s11033-019-05146-2
摘要
Glioma is the most aggressive primary brain tumor. We have previously provided evidence that IFITM3 promoted glioma cells migration. However, the mechanism of how IFITM3 regulates glioma cells invasion and whether IFITM3 participates in TGF-β-mediated glioma invasion are still unknown. In this paper, we proved that IFITM3 was notably up-regulated in glioma tissues. Knockdown of IFITM3 suppressed STAT3 phosphorylation in vitro, and a specific STAT3 inhibitor AG490 reversed IFITM3-induced invasion of glioma cells. Furthermore, IFITM3 expression was induced by TGF-β in glioma and IFITM3 knockdown abolished TGF-β-mediated glioma cells invasion. Collectively, the results indicate that IFITM3/STAT3 axis may promote TGF-β-induced glioma cells invasion. This study provided some suggestions for the clinical treatment of the brain tumor.
科研通智能强力驱动
Strongly Powered by AbleSci AI