| Literature DB >> 11034215 |
M Irwin1, M C Marin, A C Phillips, R S Seelan, D I Smith, W Liu, E R Flores, K Y Tsai, T Jacks, K H Vousden, W G Kaelin.
Abstract
The transcription factor E2F-1 induces both cell-cycle progression and, in certain settings, apoptosis. E2F-1 uses both p53-dependent and p53-independent pathways to kill cells. The p53-dependent pathway involves the induction by E2F-1 of the human tumour-suppressor protein p14ARF, which neutralizes HDM2 (human homologue of MDM2) and thereby stabilizes the p53 protein. Here we show that E2F-1 induces the transcription of the p53 homologue p73. Disruption of p73 function inhibited E2F-1-induced apoptosis in p53-defective tumour cells and in p53-/- mouse embryo fibroblasts. We conclude that activation of p73 provides a means for E2F-1 to induce death in the absence of p53.Entities:
Mesh:
Substances:
Year: 2000 PMID: 11034215 DOI: 10.1038/35036614
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962