Abstract
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 up-regulates 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 antiproliferative effects of EGR-1.
Original language | English (US) |
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Pages (from-to) | 20131-20138 |
Number of pages | 8 |
Journal | Journal of Biological Chemistry |
Volume | 272 |
Issue number | 32 |
DOIs | |
State | Published - Aug 8 1997 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Molecular Biology
- Cell Biology