FoxM1 Promotes Glioma Cells Progression by Up-Regulating Anxa1 Expression

被引:29
|
作者
Cheng, Shi-Xiang [1 ]
Tu, Yue [1 ]
Zhang, Sai [1 ]
机构
[1] CPAPF, Inst Traumat Brain Injury & Nervous Dis, Ctr Neurol & Neurosurg, Affiliated Hosp,Logist Coll, Tianjin, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 08期
基金
中国国家自然科学基金;
关键词
METASTASIS-ASSOCIATED PROTEINS; TRANSCRIPTION FACTOR; GROWTH; IDENTIFICATION; ANNEXIN-1; PROFILES; TUMORS; PROLIFERATION; ANGIOGENESIS; INHIBITION;
D O I
10.1371/journal.pone.0072376
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Forkhead box M1 (FoxM1) is a member of the forkhead transcription factor family and is overexpression in malignant gliomas. However, the molecular mechanisms by which FoxM1lead to glioma carcinogenesis and progression are still not well known. In the present study, we show that Anxa1 was overexpression in gliomas and predicted the poor outcome. Furthermore, Anxa1 closely related to the FoxM1 expression and was a direct transcriptional target of FoxM1. Overexpression of FoxM1 up-regulated Anxa1 expression, whereas suppression of FoxM1 expression down-regulated Anxa1 expression in glioma cells. Finally, FoxM1 enhanced the proliferation, migration, and angiogenesis in Anxa1-dependent manner both in vitro and in vivo. Our findings provide both clinical and mechanistic evidences that FoxM1 contributes to glioma development by directly up-regulating Anxa1 expression.
引用
收藏
页数:10
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