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首页> 外文期刊>Toxicology Letters: An International Journal Providing a Forum for Original and Pertinent Contributions in Toxicology Research >Impact of phase I or phase II enzyme polymorphisms on lymphocyte DNA adducts in subjects exposed to urban air pollution and environmental tobacco smoke.
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Impact of phase I or phase II enzyme polymorphisms on lymphocyte DNA adducts in subjects exposed to urban air pollution and environmental tobacco smoke.

机译:I或II期酶多态性对暴露于城市空气污染和环境烟草烟雾的受试者的淋巴细胞DNA加合物的影响。

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摘要

Little is known about the impact of genetic variation on the genetic damage induced by urban air pollution or environmental tobacco smoke (ETS) in exposed populations. The levels of bulky DNA adducts ( 32P-postlabelling, nuclease P1 enrichment) and chromosomal aberrations were measured in lymphocytes of 194 non-smoking students living in the city of Athens, and the rural region of Halkida, Greece. In these individuals personal exposure to PAH was also measured. Furthermore, genetic polymorphisms were examined in cytochromes P450 1A1, 1B1, in the GSTM1, GSTP1 and GSTT1 as well as in microsomal epoxy hydrolase (EPHX) genes. Subjects with the CYP1*2A mutant genotype also suffering significant ETS exposure tended to exhibit higher adduct levels and % aberrant cells. In contrast, CYP1B1 polymorphisms seemed to have an impact on the DNA adduct levels only among individual with negligible ETS exposure. Subjects carrying both the CYP1*2A mutant genotype and the GSTM1 null genotype tended to have higher DNA adduct levels. A similar effect was also observed with the combined CYP1A1*2A/GSTP1 (Ile/Val) and the CYP1A1*2A/mEH "slow" polymorphisms. In both cases, the effect was more pronounced among subjects with higher levels of ETS exposure. Stepwise restriction of the observations to subjects characterised by (a) GSTP1 mutant, (b) GSTM1 null, (c) mEH "slow" (His139His) genotypes and (d) ETS exposure resulted in a significant trend of increasing DNA adduct levels only among individuals with at least one CYP1A1*2A mutated allele, illustrating the importance and complexity of gene-exposure and gene-gene interactions in determining the level of genotoxic damage on an individual levels.
机译:关于遗传变异对暴露人群中城市空气污染或环境烟草烟雾(ETS)引起的遗传损害的影响知之甚少。测量了生活在雅典市和希腊哈尔基达农村地区的194名非吸烟学生的淋巴细胞中大体积DNA加合物(32P后标记,核酸酶P1富集)的水平和染色体畸变。在这些个体中,还测量了其对PAH的个人暴露。此外,检查了细胞色素P450 1A1、1B1,GSTM1,GSTP1和GSTT1以及微粒体环氧水解酶(EPHX)基因的遗传多态性。 CYP1 * 2A突变基因型的受试者也遭受显着的ETS暴露,倾向于表现出更高的加合物水平和%异常细胞。相反,CYP1B1多态性似乎仅对ETS暴露可忽略的个体影响DNA加合物水平。携带CYP1 * 2A突变基因型和GSTM1无效基因型的受试者倾向于具有更高的DNA加合物水平。结合CYP1A1 * 2A / GSTP1(Ile / Val)和CYP1A1 * 2A / mEH“慢”多态性,也观察到了类似的效果。在这两种情况下,ETS暴露水平较高的受试者的影响更为明显。对以(a)GSTP1突变体,(b)GSTM1 null,(c)mEH“慢”(His139His)基因型和(d)ETS暴露为特征的受试者的观察结果的逐步限制导致仅在以下情况下DNA加合物水平增加的显着趋势:具有至少一个CYP1A1 * 2A突变的等位基因的个体,说明基因暴露和基因-基因相互作用在确定单个水平的遗传毒性损害水平中的重要性和复杂性。

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