Tumor development: Haploinsufficiency and local network assembly

被引:29
作者
Smilenov, Lubomir B. [1 ]
机构
[1] Columbia Univ, Dept Radiat Oncol, Coll Phys & Surg, Ctr Radiol Res, New York, NY 10032 USA
基金
美国国家航空航天局;
关键词
tumor initiation; tumor development; haploinsufficiency; biological networks; apoptosis;
D O I
10.1016/j.canlet.2005.08.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
According to the current models, tumor development is a continuous process of mutation accumulation, leading to several intermediate phenotypes and final phases of autonomy, unlimited growth and metastasis. One of the most important events in that process is the initial destabilization of cellular pathways that subsequently allow mutations to accumulate. The mechanisms involved in that stage are not clear. In principle, the estimated very low mutation frequency in human or mouse cells would suggest that accumulating the required number of mutations for tumor development should be a statistically unlikely event. However, this theory is contradicted by the high incidence of cancers. Here we discuss the role of protein haploinsufficiency as a contributor to the initial phases of tumor development, and suggest possible mechanisms that might be involved in that process. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:17 / 28
页数:12
相关论文
共 85 条
[1]   Conditional loss of Nkx3.1 in adult mice induces prostatic intraepithelial neoplasia [J].
Abdulkadir, SA ;
Magee, JA ;
Peters, TJ ;
Kaleem, Z ;
Naughton, CK ;
Humphrey, PA ;
Milbrandt, J .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (05) :1495-1503
[2]  
[Anonymous], 1975, SEER CANC STAT REV
[3]   Haploinsufficiency of p18INK4c sensitizes mice to carcinogen-induced tumorigenesis [J].
Bai, F ;
Pei, XH ;
Godfrey, VL ;
Xiong, Y .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (04) :1269-1277
[4]   DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation [J].
Bakkenist, CJ ;
Kastan, MB .
NATURE, 2003, 421 (6922) :499-506
[5]   The genetics and genomics of cancer [J].
Balmain, A ;
Gray, J ;
Ponder, B .
NATURE GENETICS, 2003, 33 (Suppl 3) :238-244
[6]   Cancer resistance genes in mice: models for the study of tumour modifiers [J].
Balmain, A ;
Nagase, H .
TRENDS IN GENETICS, 1998, 14 (04) :139-144
[7]   Network biology:: Understanding the cell's functional organization [J].
Barabási, AL ;
Oltvai, ZN .
NATURE REVIEWS GENETICS, 2004, 5 (02) :101-U15
[8]   Emergence of scaling in random networks [J].
Barabási, AL ;
Albert, R .
SCIENCE, 1999, 286 (5439) :509-512
[9]   Radiation induced apoptosis in ataxia telangiectasia homozygote, heterozygote and normal cells [J].
Bebb, DG ;
Warrington, PJ ;
de Jong, G ;
Yu, Z ;
Moffat, JA ;
Skov, K ;
Spacey, S ;
Gelmon, K ;
Glickman, BW .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2001, 476 (1-2) :13-20
[10]   Oxidative decay of DNA [J].
Beckman, KB ;
Ames, BN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (32) :19633-19636