Genotoxic effects of asbestos in humans

被引:92
作者
Dusinská, M
Collins, A
Kazimírová, A
Barancoková, M
Harrington, V
Volkovová, K
Staruchová, M
Horská, A
Wsólová, L
Kocan, A
Petrík, J
Machata, M
Ratcliffe, B
Kyrtopoulos, S
机构
[1] Slovak Med Univ, Inst Prevent & Clin Med, Bratislava 83303, Slovakia
[2] Robert Gordon Univ, Aberdeen AB9 1FR, Scotland
[3] Univ Oslo, Dept Nutr, Oslo, Norway
[4] Natl Inst Hlth, Nitra, Slovakia
[5] Natl Hellen Res Fdn, Inst Biol Res & Biotechnol, Athens, Greece
关键词
asbestos; occupational exposure; oxidative DNA damage; DNA repair; chromosome aberrations;
D O I
10.1016/j.mrfmmm.2004.06.027
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
Risks of carcinogenic and non-carcinogenic effects from asbestos continue owing to the persistence of the fibres in building materials and other products. For this reason, epidemiological and mechanistic research on the toxic effects of asbestos and mineral fibres is still needed. The present molecular epidemiological study was conducted in a former asbestos cement plant in Slovakia. Altogether 82 subjects were investigated, 61 exposed subjects (24 smokers and 37 nor-smokers), and 21 factory controls (8 smokers and 13 non-smokers). Workers were exposed to asbestos for between 5 and 40 years. Though the exposure to asbestos during past 40 years was relatively high, at the time of sampling the concentrations of asbestos in the production hall exceeded the Slovak occupational limit (0.001 fibre/cm(3)) by a factor of only 3-5. The office area levels were below this limit. Biomarkers of exposure, effect and individual susceptibility were measured, including DNA damage (strand breaks [SBs], base oxidation and alkylation, using the comet assay); cytogenctic parameters; and individual DNA repair capacity (incision at 8-oxoguanine measured using a modified comet assay). Oxidised pyrimidines were significantly higher in exposed men compared with non-exposed (P = 0.04). There was also a positive association between S Bs (P = 0.04) and age, and alkylation damage to DNA(P= 0.04) and age. Moreover, oxidised pyrimidines (P= 0.01) and alkylated bases (P = 0.001) strongly correlated with years of occupational exposure. Micronucleus frequency did not differ between exposed and control subjects. Repair capacity overall did not show any effect of exposure, though female controls had higher incision rates than did female exposed subjects. However, exposed asbestos workers had significantly higher numbers of chromosomal aberrations (P = 0.01) compared with control group. This finding is consistent with the known association of chromosome aberrations with cancer-risk. (C) 2004 Published by Elsevier B.V.
引用
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页码:91 / 102
页数:12
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