p53: At the crossroad between cancer and ageing

被引:60
作者
Papazoglu, C.
Mills, A. A. [1 ]
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] SUNY Stony Brook, Stony Brook, NY 11794 USA
关键词
p53; senescence; ageing; mouse models;
D O I
10.1002/path.2086
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The p53 tumour suppressor plays an undisputed role in cancer. p53's tumour suppressive activity stems from its ability to respond to a variety of stresses to trigger cell cycle arrest, apoptosis or senescence, thereby protecting against malignant transformation. An increasing body of evidence suggests that p53 also drives organismal ageing. Although genetic models with altered p53 function display age-related phenotypes and thus provide in vivo evidence that p53 contributes to the ageing process, p53's role in organismal ageing remains controversial. Anti-cancer therapies that target p53 and reactivate or enhance its activity are considered good alternatives for treating various neoplasms. Therefore, it is important to determine whether these clinical approaches compromise tissue homeostasis and contribute to ageing. This review presents a number of models with altered p53 function and discusses how these models implicate p53 as part of a molecular network that integrates tumour suppression and ageing. Copyright (c) 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:124 / 133
页数:10
相关论文
共 74 条
[1]   Testicular wild-type p53 expression in transgenic mice induces spermiogenesis alterations ranging from differentiation defects to apoptosis [J].
Allemand, I ;
Anglo, A ;
Jeantet, AY ;
Cerutti, I ;
May, E .
ONCOGENE, 1999, 18 (47) :6521-6530
[2]   Neuronal expression of p53 dominant-negative proteins in adult Drosophila melanogaster extends life span [J].
Bauer, JH ;
Poon, PC ;
Glatt-Deeley, H ;
Abrams, JM ;
Helfand, SL .
CURRENT BIOLOGY, 2005, 15 (22) :2063-2068
[3]   Reversal of human cellular senescence:: roles of the p53 and p16 pathways [J].
Beauséjour, CM ;
Krtolica, A ;
Galimi, F ;
Narita, M ;
Lowe, SW ;
Yaswen, P ;
Campisi, J .
EMBO JOURNAL, 2003, 22 (16) :4212-4222
[4]   iASPP oncoprotein is a key inhibitor of p53 conserved from worm to human [J].
Bergamaschi, D ;
Samuels, Y ;
O'Neil, NJ ;
Trigiante, G ;
Crook, T ;
Hsieh, JK ;
O'Connor, DJ ;
Zhong, S ;
Campargue, I ;
Tomlinson, ML ;
Kuwabara, PE ;
Lu, X .
NATURE GENETICS, 2003, 33 (02) :162-167
[5]   Telomeres in cancer and aging: lessons from the mouse [J].
Blasco, MA .
CANCER LETTERS, 2003, 194 (02) :183-188
[6]   Telomere shortening and tumor formation by mouse cells lacking telomerase RNA [J].
Blasco, MA ;
Lee, HW ;
Hande, MP ;
Samper, E ;
Lansdorp, PM ;
DePinho, RA ;
Greider, CW .
CELL, 1997, 91 (01) :25-34
[7]   Extended longevity in mice lacking the insulin receptor in adipose tissue [J].
Blüher, M ;
Kahn, BB ;
Kahn, CR .
SCIENCE, 2003, 299 (5606) :572-574
[8]   A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans [J].
Bond, GL ;
Hu, WW ;
Bond, EE ;
Robins, H ;
Lutzker, SG ;
Arva, NC ;
Bargonetti, J ;
Bartel, F ;
Taubert, H ;
Wuerl, P ;
Onel, K ;
Yip, L ;
Hwang, SJ ;
Strong, LC ;
Lozano, G ;
Levine, AJ .
CELL, 2004, 119 (05) :591-602
[9]   p53 isoforms can regulate p53 transcriptional activity [J].
Bourdon, JC ;
Fernandes, K ;
Murray-Zmijewski, F ;
Liu, G ;
Diot, A ;
Xirodimas, DP ;
Saville, MK ;
Lane, DP .
GENES & DEVELOPMENT, 2005, 19 (18) :2122-2137
[10]   Bypass of senescence after disruption of p21(CIP1/WAF1) gene in normal diploid human fibroblasts [J].
Brown, JP ;
Wei, WY ;
Sedivy, JM .
SCIENCE, 1997, 277 (5327) :831-834