The p53 response to DNA damage

被引:277
作者
Meek, DW [1 ]
机构
[1] Univ Dundee, Ninewells Hosp & Med Sch, Biomed Res Ctr, Dundee DD1 9SY, Scotland
关键词
p53; MDM2; growth arrest; apoptosis;
D O I
10.1016/j.dnarep.2004.03.027
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The p53 tumour suppressor protein is a highly potent transcription factor which, under normal circumstances, is maintained at low levels through the action of MDM2, an E3 ubiquitin ligase which directs p53 ubiquitylation and degradation. Expression of the mdm2 gene is Stimulated by p53 and this reciprocal relationship forms the basis of a negative feedback loop. Both genotoxic and non-genotoxic stresses that induce p53 focus principally on interruption of the p53-MDM2 loop with the consequence that p53 becomes stabilised, leading to changes in the expression of p53-responsive genes. The biological outcome of inducing this pathway can be either growth arrest or apoptosis: factors affecting the functioning of the loop, the biochemical activity of p53 itself and the cellular environment govern the choice between these Outcomes in a cell type- and stress-specific manner. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1049 / 1056
页数:8
相关论文
共 45 条
[1]   Post-translational modifications and activation of p53 by genotoxic stresses [J].
Appella, E ;
Anderson, CW .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (10) :2764-2772
[2]   Stress signals utilize multiple pathways to stabilize p53 [J].
Ashcroft, M ;
Taya, Y ;
Vousden, KH .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (09) :3224-3233
[3]   Regulation of p53 stability [J].
Ashcroft, M ;
Vousden, KH .
ONCOGENE, 1999, 18 (53) :7637-7643
[4]   Design of a synthetic Mdm2-binding mini protein that activates the p53 response in vivo [J].
Bottger, A ;
Bottger, V ;
Sparks, A ;
Liu, WL ;
Howard, SF ;
Lane, DP .
CURRENT BIOLOGY, 1997, 7 (11) :860-869
[5]   Direct interactions between HIF-1α and Mdm2 modulate p53 function [J].
Chen, DL ;
Li, MY ;
Luo, JY ;
Gu, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (16) :13595-13598
[6]   p53 levels, functional domains, and DNA damage determine the extent of the apoptotic response of tumor cells [J].
Chen, XB ;
Ko, LJ ;
Jayaraman, L ;
Prives, C .
GENES & DEVELOPMENT, 1996, 10 (19) :2438-2451
[7]   A small synthetic peptide, which inhibits the p53-hdm2 interaction, stimulates the p53 pathway in tumour cell lines [J].
Chène, P ;
Fuchs, J ;
Bohn, J ;
García-Echeverría, C ;
Furet, P ;
Fabbro, D .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 299 (01) :245-253
[8]   Study of the cytotoxic effect of a peptidic inhibitor of the p53-hdm2 interaction in tumor cells [J].
Chène, P ;
Fuchs, J ;
Carena, I ;
Furet, P ;
Echeverria, CG .
FEBS LETTERS, 2002, 529 (2-3) :293-297
[9]   The loss of mdm2 induces p53 mediated apoptosis [J].
de Rozieres, S ;
Maya, R ;
Oren, M ;
Lozano, G .
ONCOGENE, 2000, 19 (13) :1691-1697
[10]   E1A signaling to p53 involves the p19ARF tumor suppressor [J].
de Stanchina, E ;
McCurrach, ME ;
Zindy, F ;
Shieh, SY ;
Ferbeyre, G ;
Samuelson, AV ;
Prives, C ;
Roussel, MF ;
Sherr, CJ ;
Lowe, SW .
GENES & DEVELOPMENT, 1998, 12 (15) :2434-2442