Oxidative DNA and protein damage in metal-induced toxicity and carcinogenesis

被引:185
作者
Kasprzak, KS [1 ]
机构
[1] NCI, Comparat Carcinogenesis Lab, Frederick, MD 21701 USA
关键词
carcinogenesis; DNA; histories; metals; oxidative damage; oxygen radicals; proteins; radicals; toxicity; free radicals;
D O I
10.1016/S0891-5849(02)00809-2
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
This review discusses the relevance of oxidative damage to metal-induced toxicity and carcinogenesis. Presented are important facts and mechanistic concepts on the capacity of selected transition metals, mainly Ni, but also Cu, Co, Cr, and briefly several others, to generate active oxygen species, and other reactive intermediates under physiological conditions. These metals are known to be toxic and/or carcinogenic contaminants of the occupational and general environments. Their redox activity may underlay the mechanism of mediation of oxidative damage to cell constituents. The presentation is focused on selected issues relative to genetic and epigenetic toxicity and illustrated with examples of metal-mediated oxidative damage to the principal components of chromatin, i.e., DNA, histones, and protamines. Published by Elsevier Science Inc.
引用
收藏
页码:958 / 967
页数:10
相关论文
共 42 条
[1]  
[Anonymous], 1988, BIOINORGANIC CHEM NI
[2]  
[Anonymous], TOXICOLOGY METALS
[3]  
[Anonymous], 1974, J COORD CHEM
[4]   Mechanisms of DNA oxidation [J].
Aust, AE ;
Eveleigh, JF .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1999, 222 (03) :246-252
[5]   Induction of a secondary structure in the N-terminal pentadecapeptide of human protamine HP2 through Ni(II) coordination.: An NMR study [J].
Bal, W ;
Wójcik, J ;
Maciejczyk, M ;
Grochowski, P ;
Kasprzak, KS .
CHEMICAL RESEARCH IN TOXICOLOGY, 2000, 13 (09) :823-830
[6]   Binding of nickel(II) and copper(II) to the N-terminal sequence of human protamine HP2 [J].
Bal, W ;
JezowskaBojczuk, M ;
Kasprzak, KS .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (08) :906-914
[7]   Interactions of nickel(II) with histones:: Interactions of Nickel(II) with CH3CO-Thr-Glu-Ser-His-His-Lys-NH2, a peptide modeling the potential metal binding site in the "C-Tail" region of histone H2A [J].
Bal, W ;
Lukszo, J ;
Bialkowski, K ;
Kasprzak, KS .
CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (09) :1014-1023
[8]   Mediation of oxidative DNA damage by nickel(II) and copper(II) complexes with the N-terminal sequence of human protamine HP2 [J].
Bal, W ;
Lukszo, J ;
Kasprzak, KS .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (08) :915-921
[9]   Ni(II) specifically cleaves the C-terminal tail of the major variant of histone H2A and forms an oxidative damage mediating complex with the cleaved-off octapeptide [J].
Bal, W ;
Liang, RT ;
Lukszo, J ;
Lee, SH ;
Dizdaroglu, M ;
Kasprzak, KS .
CHEMICAL RESEARCH IN TOXICOLOGY, 2000, 13 (07) :616-624
[10]  
Buzard Gregory S., 2000, Journal of Environmental Pathology Toxicology and Oncology, V19, P179