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砷(+3氧化态)甲基转移酶(AS3MT)变体与无机砷尿代谢产物之间的关联:暴露水平的作用。

Association Between Variants in Arsenic (+3 Oxidation State) Methyltranserase (AS3MT) and Urinary Metabolites of Inorganic Arsenic: Role of Exposure Level.

作者信息

Xu Xiaofan, Drobná Zuzana, Voruganti V Saroja, Barron Keri, González-Horta Carmen, Sánchez-Ramírez Blanca, Ballinas-Casarrubias Lourdes, Cerón Roberto Hernández, Morales Damián Viniegra, Terrazas Francisco A Baeza, Ishida María C, Gutiérrez-Torres Daniela S, Saunders R Jesse, Crandell Jamie, Fry Rebecca C, Loomis Dana, García-Vargas Gonzalo G, Del Razo Luz M, Stýblo Miroslav, Mendez Michelle A

机构信息

*Department of Nutrition, Gillings School of Global Public Health.

Department of Biological Sciences College of Sciences, North Carolina State University, North Carolina.

出版信息

Toxicol Sci. 2016 Sep;153(1):112-23. doi: 10.1093/toxsci/kfw112. Epub 2016 Jun 30.

Abstract

Variants in AS3MT, the gene encoding arsenic (+3 oxidation state) methyltranserase, have been shown to influence patterns of inorganic arsenic (iAs) metabolism. Several studies have suggested that capacity to metabolize iAs may vary depending on levels of iAs exposure. However, it is not known whether the influence of variants in AS3MT on iAs metabolism also vary by level of exposure. We investigated, in a population of Mexican adults exposed to drinking water As, whether associations between 7 candidate variants in AS3MT and urinary iAs metabolites were consistent with prior studies, and whether these associations varied depending on the level of exposure. Overall, associations between urinary iAs metabolites and AS3MT variants were consistent with the literature. Referent genotypes, defined as the genotype previously associated with a higher percentage of urinary dimethylated As (DMAs%), were associated with significant increases in the DMAs% and ratio of DMAs to monomethylated As (MAs), and significant reductions in MAs% and iAs%. For 3 variants, associations between genotypes and iAs metabolism were significantly stronger among subjects exposed to water As >50 versus ≤50 ppb (water As X genotype interaction P < .05). In contrast, for 1 variant (rs17881215), associations were significantly stronger at exposures ≤50 ppb. Results suggest that iAs exposure may influence the extent to which several AS3MT variants affect iAs metabolism. The variants most strongly associated with iAs metabolism-and perhaps with susceptibility to iAs-associated disease-may vary in settings with exposure level.

摘要

编码砷(+3氧化态)甲基转移酶的AS3MT基因中的变异已被证明会影响无机砷(iAs)的代谢模式。多项研究表明,iAs的代谢能力可能因iAs暴露水平而异。然而,尚不清楚AS3MT基因变异对iAs代谢的影响是否也会因暴露水平而有所不同。我们在一群接触饮用水中砷的墨西哥成年人中进行了调查,以研究AS3MT基因中的7个候选变异与尿中iAs代谢物之间的关联是否与先前的研究一致,以及这些关联是否会因暴露水平而有所不同。总体而言,尿中iAs代谢物与AS3MT基因变异之间的关联与文献一致。参照基因型(定义为先前与较高百分比的尿二甲基砷(DMAs%)相关的基因型)与DMAs%以及DMAs与一甲基砷(MAs)的比率显著增加,而MAs%和iAs%显著降低有关。对于3个变异,在接触水中砷>50 ppb与≤50 ppb的受试者中,基因型与iAs代谢之间的关联显著更强(水砷×基因型交互作用P<0.05)。相比之下,对于1个变异(rs17881215),在暴露水平≤50 ppb时关联显著更强。结果表明,iAs暴露可能会影响多个AS3MT基因变异对iAs代谢的影响程度。与iAs代谢以及可能与iAs相关疾病易感性最密切相关的变异可能会因暴露水平不同而有所差异。

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