The role of oxidative stress in carcinogenesis

被引:1120
作者
Klaunig, JE [1 ]
Kamendulis, LM [1 ]
机构
[1] Indiana Univ, Sch Med, Dept Pharmacol & Toxicol, Indianapolis, IN 46202 USA
关键词
cancer; reactive oxygen species; oxidative DNA damage; apoptosis; cell proliferation; gene expression; signal transduction;
D O I
10.1146/annurev.pharmtox.44.101802.121851
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chemical carcinogenesis follows a multistep process involving both mutation and increased cell proliferation. Oxidative stress can occur through overproduction of reactive oxygen and nitrogen species through either endogenous or exogenous insults. Important to carcinogenesis, the unregulated or prolonged production of cellular oxidants has been linked to mutation (induced by oxidant-induced DNA damage), as well as modification of gene expression. In particular, signal transduction. pathways, including AP-1 and NFkappaB, are known to be activated by reactive oxygen species, and they lead to the transcription of genes involved in cell growth regulatory pathways. This review examines the evidence of cellular oxidants' involvement in the carcinogenesis process, and focuses on the mechanisms for production, cellular damage produced, and the role of signaling cascades by reactive oxygen species.
引用
收藏
页码:239 / 267
页数:29
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共 186 条
  • [1] ABANOBI SE, 1982, CANCER RES, V42, P412
  • [2] Methods for monitoring oxidative stress, lipid peroxidation and oxidation resistance of lipoproteins
    Abuja, PM
    Albertini, R
    [J]. CLINICA CHIMICA ACTA, 2001, 306 (1-2) : 1 - 17
  • [3] Role of redox potential and reactive oxygen species in stress signaling
    Adler, V
    Yin, ZM
    Tew, KD
    Ronai, Z
    [J]. ONCOGENE, 1999, 18 (45) : 6104 - 6111
  • [4] AGGARWAL BB, 1992, TUMOR NECROSIS FACTOR : STRUCTURE-FUNCTION RELATIONSHIP AND CLINICAL APPLICATION, P191
  • [5] Alliangana DMI, 1996, E AFR MED J, V73, P752
  • [6] TOO MANY RODENT CARCINOGENS - MITOGENESIS INCREASES MUTAGENESIS
    AMES, BN
    GOLD, LS
    [J]. SCIENCE, 1990, 249 (4972) : 970 - 971
  • [7] AMSTAD PA, 1992, CANCER RES, V52, P3952
  • [8] [Anonymous], 1985, OXIDATIVE STRESS
  • [9] [Anonymous], 1997, FREE RADICAL TOXICOL
  • [10] Generation of free radicals during lipid hydroperoxide-triggered apoptosis in PC12h cells
    Aoshima, H
    Satoh, T
    Sakai, N
    Yamada, M
    Enokido, Y
    Ikeuchi, T
    Hatanaka, H
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1997, 1345 (01): : 35 - 42