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中国氯乙烯接触工人染色体损伤和代谢及 DNA 修复基因易感基因型的流行和持久性。

Prevalence and persistence of chromosomal damage and susceptible genotypes of metabolic and DNA repair genes in Chinese vinyl chloride-exposed workers.

机构信息

Department of Occupational Health and Toxicology, School of Public Health, Fudan University, China.

出版信息

Carcinogenesis. 2010 Apr;31(4):648-53. doi: 10.1093/carcin/bgq015. Epub 2010 Jan 25.

Abstract

Vinyl chloride (VC) was classified as a group 1 carcinogen by IARC in 1987. Although the relationship between VC exposure and liver cancer has been established, the mechanism of VC-related carcinogenesis remains largely unknown. Previous epidemiological studies have shown that VC exposure is associated with increased genotoxicity in humans. To explore chromosomal damage and its progression, and their association to genetic susceptibility, we investigated 402 workers exposed to VC, a 77 VC-exposed cohort and 141 unexposed subjects. We measured the frequencies of cytokinesis-block micronucleus (CBMN) to reflect chromosomal damage and conducted genotyping for six xenobiotic metabolisms and five DNA repair genes' polymorphism. Data indicate that 95% of the control workers had CBMN frequencies </=3 per thousand, whereas VC-exposed workers had the 3.73-fold increase compared with the controls. Among the cohort workers who were followed from 2004 to 2007, the mean CBMN frequency was higher in 2007 than in 2004 with ratio of 2.08. Multiple Poisson regression analysis showed that mean CBMN frequencies were significantly elevated for the intermediate and high exposure groups than the low. Exposed workers with CYP2E1 or XRCC1 variance showed a higher CBMN frequency than their wild-type homozygous counterparts, so did workers with GSTP1 or ALDH2 genotype. This study provides evidence that cumulative exposure dose of VC and common genetic variants in genes relevant to detoxification of carcinogens are the major factors that modulate CBMN induction in VC-exposed workers.

摘要

氯乙烯(VC)于 1987 年被 IARC 归类为 1 类致癌物。虽然 VC 暴露与肝癌之间的关系已经确立,但 VC 相关致癌的机制在很大程度上仍然未知。先前的流行病学研究表明,VC 暴露与人的遗传毒性增加有关。为了探讨染色体损伤及其进展及其与遗传易感性的关系,我们调查了 402 名接触 VC 的工人,包括 77 名 VC 暴露队列和 141 名未暴露的工人。我们测量了细胞有丝分裂阻断微核(CBMN)的频率,以反映染色体损伤,并对六种外源物质代谢和五种 DNA 修复基因的多态性进行了基因分型。数据表明,95%的对照工人的 CBMN 频率</=3 每千,而 VC 暴露工人的 CBMN 频率比对照组增加了 3.73 倍。在 2004 年至 2007 年随访的队列工人中,2007 年的平均 CBMN 频率高于 2004 年,比值为 2.08。多泊松回归分析显示,中、高暴露组的平均 CBMN 频率显著高于低暴露组。与野生型纯合子相比,CYP2E1 或 XRCC1 变异的暴露工人的 CBMN 频率较高,GSTP1 或 ALDH2 基因型的工人也是如此。这项研究提供了证据,证明 VC 的累积暴露剂量和与致癌物解毒相关的基因中的常见遗传变异是调节 VC 暴露工人中 CBMN 诱导的主要因素。

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