Guilt by association? p53 and the development of aneuploidy in cancer

被引:70
作者
Duensing, A
Duensing, S [1 ]
机构
[1] Univ Pittsburgh, Inst Canc, Mol Virol Program, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15213 USA
关键词
D O I
10.1016/j.bbrc.2005.03.157
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
Aneuploidy is one of the most frequent genetic alterations in solid tumors. It is commonly caused by cell division errors that are induced by oncogene activation or loss of tumor suppressor functions. In addition, certain viral oncoproteins have been implicated in the induction of chromosome copy number changes. Aneuploidy and inactivation of p53 frequently coincide in human cancers but there is increasing evidence that loss of p53 by itself is not a primary cause of aneuploidy. Nonetheless, p53 inactivation synergizes with additional oncogenic events to promote aneuploidy and may facilitate chromosomal imbalances through indirect mechanisms. This review summarizes the current knowledge about the association between aneuploidy and p53, and discusses two of the most controversial mechanisms that have been implicated in genomic instability associated with loss of p53: subversion of ploidy control and aberrant centrosome duplication. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:694 / 700
页数:7
相关论文
共 79 条
[1]   Tetraploid state induces p53-dependent arrest of nontransformed mammalian cells in G1 [J].
Andreassen, PR ;
Lohez, OD ;
Lacroix, FB ;
Margolis, RL .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (05) :1315-1328
[2]   Evolution of neoplastic cell lineages in Barrett oesophagus [J].
Barrett, MT ;
Sanchez, CA ;
Prevo, LJ ;
Wong, DJ ;
Galipeau, PC ;
Paulson, TG ;
Rabinovitch, PS ;
Reid, BJ .
NATURE GENETICS, 1999, 22 (01) :106-109
[3]  
BLOUNT PL, 1991, CANCER RES, V51, P5482
[4]  
BLOUNT PL, 1994, CANCER RES, V54, P2292
[5]   Multiple centrosomes arise from tetraploidy checkpoint failure and mitotic centrosome clusters in p53 and RB pocket protein-compromised cells [J].
Borel, F ;
Lohez, OD ;
Lacroix, FB ;
Margolis, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (15) :9819-9824
[6]   Inactivation of p53 tumor suppressor gene acts synergistically with c-neu oncogene in salivary gland tumorigenesis [J].
Brodie, SG ;
Xu, XL ;
Li, CL ;
Kuo, A ;
Leder, P ;
Deng, CX .
ONCOGENE, 2001, 20 (12) :1445-1454
[7]   BOTH VIRAL (ADENOVIRUS E1B) AND CELLULAR (HSP-70, P53) COMPONENTS INTERACT WITH CENTROSOMES [J].
BROWN, CR ;
DOXSEY, SJ ;
WHITE, E ;
WELCH, WJ .
JOURNAL OF CELLULAR PHYSIOLOGY, 1994, 160 (01) :47-60
[8]  
Bunz F, 2002, CANCER RES, V62, P1129
[9]   Genetic instability and darwinian selection in tumours (Reprinted from Trends in Biochemical Science, vol 12, Dec., 1999) [J].
Cahill, DP ;
Kinzler, KW ;
Vogelstein, B ;
Lengauer, C .
TRENDS IN CELL BIOLOGY, 1999, 9 (12) :M57-M60
[10]   Acquisition of multiple copies of a mutant topoisomerase II alpha allele by chromosome 17 aneuploidy is associated with etoposide resistance in human melanoma cell lines [J].
Campain, JA ;
Slovak, ML ;
Schoenlein, PV ;
Popescu, NC ;
Gottesman, MM ;
Pastan, I .
SOMATIC CELL AND MOLECULAR GENETICS, 1995, 21 (06) :451-471