Early growth response-1-dependent apoptosis is mediated by p53

被引:170
作者
Nair, P
Muthukkumar, S
Sells, SF
Han, SS
Sukhatme, VP
Rangnekar, VM
机构
[1] UNIV KENTUCKY,DEPT SURG,DIV UROL,LEXINGTON,KY 40536
[2] UNIV KENTUCKY,DEPT MICROBIOL & IMMUNOL,LEXINGTON,KY 40536
[3] UNIV KENTUCKY,GRAD CTR TOXICOL,LEXINGTON,KY 40536
[4] UNIV KENTUCKY,MARKEY CANC CTR,LEXINGTON,KY 40536
[5] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02215
[6] BETH ISRAEL DEACONESS MED CTR,DIV RENAL,BOSTON,MA 02215
关键词
D O I
10.1074/jbc.272.32.20131
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 early growth response-1 (EGR-1) protein is an anti-proliferative signal for certain tumor cells and is required for apoptosis induced by stimuli that elevate intracellular Ca2+. We present evidence that EGR-1 transactivates the promoter of the p53 gene and upregulates p53 RNA and protein levels. Inhibition of p53 function with dominant-negative p53 mutants abrogates EGR-1-dependent apoptosis. These findings establish a direct functional link between EGR-1 and the p53-mediated cell death pathway and suggest that mutant forms of p53 in tumor cells may provide resistance to the anti-proliferative effects of EGR-1.
引用
收藏
页码:20131 / 20138
页数:8
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