Some p53-binding proteins that can function as arbiters of life and death

被引:75
作者
Braithwaite, A. W.
Del Sal, G.
Lu, X.
机构
[1] Univ Otago, Sch Med, Dept Pathol, Dunedin 9001, New Zealand
[2] Univ Trieste, LNCIB, Area Sci Pk, Trieste, Italy
[3] Univ Trieste, Dipartimento Biochim Biofis & Chim Macromol, I-34127 Trieste, Italy
[4] UCL Branch, Ludwig Inst Canc Res, London, England
关键词
p53; E2F; ASPP; YB1; Pin1;
D O I
10.1038/sj.cdd.4401924
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
Four sets of p53-binding proteins are discussed in this review. These are the E2F family, the ASPP family, Y-box-binding protein YB1, and the prolyl isomerase Pin1. Each appears to play a role in the decision by p53 to induce an arrest of cell proliferation or apoptosis and they may also be independent markers of cancer. Their activities appear to be linked with the cell cycle and they may also interact with each other. In this review, the properties of each protein class are discussed as well as how they affect p53 functions. A model is proposed as to how their activities might be coordinated.
引用
收藏
页码:984 / 993
页数:10
相关论文
共 80 条
[1]   Nuclear localization and increased levels of transcription factor YB-1 in primary human breast cancers are associated with intrinsic MDR1 gene expression [J].
Bargou, RC ;
Jurchott, K ;
Wagener, C ;
Bergmann, S ;
Metzner, S ;
Bommert, K ;
Mapara, MY ;
Winzer, KJ ;
Dietel, M ;
Dorken, B ;
Royer, HD .
NATURE MEDICINE, 1997, 3 (04) :447-450
[2]   p14ARF links the tumour suppressors RB and p53 [J].
Bates, S ;
Phillips, AC ;
Clark, PA ;
Stott, F ;
Peters, G ;
Ludwig, RL ;
Vousden, KH .
NATURE, 1998, 395 (6698) :124-125
[3]   ASPP1 and ASPP2: Common activators of p53 family members [J].
Bergamaschi, D ;
Samuels, Y ;
Jin, BQ ;
Duraisingham, S ;
Crook, T ;
Lu, X .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (03) :1341-1350
[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]   Mutations in proline 82 of p53 impair its activation by Pin1 and Chk2 in response to DNA damage [J].
Berger, M ;
Stahl, N ;
Del Sal, G ;
Haupt, Y .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (13) :5380-5388
[6]   YB-1 provokes breast cancer through the induction of chromosomal instability that emerges from mitotic failure and centrosome amplification [J].
Bergmann, S ;
Royer-Pokora, B ;
Fietze, E ;
Jürchott, K ;
Hildebrandt, B ;
Trost, D ;
Leenders, F ;
Claude, JC ;
Theuring, F ;
Bargou, R ;
Dietel, M ;
Royer, HD .
CANCER RESEARCH, 2005, 65 (10) :4078-4087
[7]   Y-box-binding protein 1 confers EGF independence to human mammary epithelial cells [J].
Berquin, IM ;
Pang, B ;
Dziubinski, ML ;
Scott, LM ;
Chen, YQ ;
Nolan, GP ;
Ethier, SP .
ONCOGENE, 2005, 24 (19) :3177-3186
[8]   The p53 story: layers of complexity [J].
Braithwaite, AW ;
Royds, JA ;
Jackson, P .
CARCINOGENESIS, 2005, 26 (07) :1161-1169
[9]   Phosphorylation of human p53 by p38 kinase coordinates N-terminal phosphorylation and apoptosis in response to UV radiation [J].
Bulavin, DV ;
Saito, S ;
Hollander, MC ;
Sakaguchi, K ;
Anderson, CW ;
Appella, E ;
Fornace, AJ .
EMBO JOURNAL, 1999, 18 (23) :6845-6854
[10]   DNA damage-dependent acetylation of p73 dictates the selective activation of apoptotic target genes [J].
Costanzo, A ;
Merlo, P ;
Pediconi, N ;
Fulco, M ;
Sartorelli, V ;
Cole, PA ;
Fontemaggi, G ;
Fanciulli, M ;
Schiltz, L ;
Blandino, G ;
Balsano, C ;
Levrero, M .
MOLECULAR CELL, 2002, 9 (01) :175-186