The Egr-1 transcription factor directly activates PTEN during irradiation-induced signalling

被引:348
作者
Virolle, T
Adamson, ED
Baron, V
Birle, D
Mercola, D
Mustelin, T
de Belle, I
机构
[1] Burnham Inst, Canc Res Ctr, La Jolla, CA 92037 USA
[2] Sidney Kimmel Canc Ctr, San Diego, CA 92121 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ncb1201-1124
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The PTEN tumour suppressor(1) and pro-apoptotic(2) gene is frequently mutated in human cancers. We show that PTEN transcription is upregulated by Egr-1 after irradiation in wild-type, but not egr-1(-/-), mice in vivo. We found that Egr-1 specifically binds to the PTEN 5' untranslated region, which contains a functional GCGGCGGCG Egr-1-binding site. Inducing Egr-1 by exposing cells to ultraviolet light upregulates expression of PTEN messenger RNA and protein, and leads to apoptosis. egr-1(-/-) cells, which cannot upregulate PTEN expression after irradiation, are resistant to ultraviolet-light-induced apoptosis. Therefore, Egr-1 can directly regulate PTEN, triggering the initial step in this apoptotic pathway. Loss of Egr-1 expression, which often occurs in human cancers, could deregulate the PTEN gene and contribute to the radiation resistance of some cancer cells.
引用
收藏
页码:1124 / 1128
页数:5
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