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

机译:接触氯乙烯的中国工人染色体损伤的普遍性和持久性以及代谢和DNA修复基因的易感基因型

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摘要

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‰, 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.
机译:1987年,IARC将氯乙烯(VC)归类为第1类致癌物。尽管已经建立了VC暴露与肝癌之间的关系,但是与VC相关的致癌机制仍很未知。先前的流行病学研究表明,VC暴露与人类遗传毒性增加有关。为了探索染色体损伤及其进展,以及它们与遗传易感性的关系,我们调查了402名暴露于VC的工人,77名暴露于VC的队列和141名未暴露的受试者。我们测量了胞质分裂阻滞微核(CBMN)的频率以反映染色体损伤,并进行了六个异种生物代谢和五个DNA修复基因多态性的基因分型。数据表明,有95%的对照工作者的CBMN频率≤3‰,而暴露于VC的工作者与对照者相比增加了3.73倍。在2004年至2007年追踪的队列研究人员中,2007年CBMN的平均发生频率高于2004年,比率为2.08。多重Poisson回归分析显示,中高暴露组的CBMN平均频率显着高于低暴露组。暴露于CYP2E1或XRCC1变异的工人显示CBMN频率高于其野生型纯合子工人,具有GSTP1或ALDH2基因型的工人也是如此。这项研究提供的证据表明,与致癌物解毒相关的基因中VC的累积暴露剂量和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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