Genetic instability and the tumor microenvironment: towards the concept of microenvironment-induced mutagenesis

被引:116
作者
Bindra, RS
Glazer, PM
机构
[1] Yale Univ, Sch Med, Dept Therapeut Radiol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Expt Pathol, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06520 USA
关键词
genetic instability; microenvironment; hypoxia; DNA repair;
D O I
10.1016/j.mrfmmm.2004.03.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
It has been well established that tumor progression is correlated with genetic instability. Growing evidence suggests that the tumor microenvironment itself constitutes a significant source of such genetic instability. The adverse conditions of this microenvironment are associated with the induction of mutagenesis and numerous types of DNA damage. including DNA strand breaks and oxidative base damage. While such DNA lesions pose a significant threat to genome integrity, recent studies now suggest that genetic instability in the tumor rnicroenvironrnent also may arise front the dysregulation of DNA repair pathways. In this review, we will summarize the case for the tumor microenvironment as a key culprit in the induction of genetic instability and the potential mechanisms by which this phenomenon occurs. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 85
页数:11
相关论文
共 79 条
  • [1] Multiple sites required for expression in 5′-flanking region of the hMLH1 gene
    Arita, M
    Zhong, XL
    Min, ZH
    Hemmi, H
    Shimatake, H
    [J]. GENE, 2003, 306 : 57 - 65
  • [2] Antiangiogenic therapy and tumor progression
    Blagosklonny, MV
    [J]. CANCER CELL, 2004, 5 (01) : 13 - 17
  • [3] GENE AMPLIFICATION AND TUMOR PROGRESSION
    BRISON, O
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1155 (01) : 25 - 41
  • [4] Brizel DM, 1996, CANCER RES, V56, P5347
  • [5] Oxidative stress inactivates the human DNA mismatch repair system
    Chang, CL
    Marra, G
    Chauhan, DP
    Ha, HT
    Chang, DK
    Ricciardiello, L
    Randolph, A
    Carethers, JM
    Boland, CR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 283 (01): : C148 - C154
  • [6] Steady-state regulation of the human DNA mismatch repair system
    Chang, DK
    Ricciardiello, L
    Goel, A
    Chang, CL
    Boland, CR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (24) : 18424 - 18431
  • [7] PERSISTENTLY ELEVATED FREQUENCY OF SPONTANEOUS MUTATIONS IN PROGENY OF CHO CLONES SURVIVING X-IRRADIATION - ASSOCIATION WITH DELAYED REPRODUCTIVE DEATH PHENOTYPE
    CHANG, WSP
    LITTLE, JB
    [J]. MUTATION RESEARCH, 1992, 270 (02): : 191 - 199
  • [8] A new role for hypoxia in tumor progression: Induction of fragile site triggering genomic rearrangements and formation of complex DMs and HSRs
    Coquelle, A
    Toledo, F
    Stern, S
    Bieth, A
    Debatisse, M
    [J]. MOLECULAR CELL, 1998, 2 (02) : 259 - 265
  • [9] Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons
    Coquelle, A
    Pipiras, E
    Toledo, F
    Buttin, G
    Debatisse, M
    [J]. CELL, 1997, 89 (02) : 215 - 225
  • [10] Induction of multiple double-strand breaks within an hsr by meganuclease I-SceI expression or fragile site activation leads to formation of double minutes and other chromosomal rearrangements
    Coquelle, A
    Rozier, L
    Dutrillaux, B
    Debatisse, M
    [J]. ONCOGENE, 2002, 21 (50) : 7671 - 7679