| Autor: |
Agusa T; Center for Marine Environmental Studies (CMES), Ehime University., Kunito T, Minh Tue N, Thi Mai Lan V, Binh Minh T, Thi Kim Trang P, Fujihara J, Takeshita H, Takahashi S, Hung Viet P, Tanabe S, Iwata H |
| Jazyk: |
japonština |
| Zdroj: |
Nihon eiseigaku zasshi. Japanese journal of hygiene [Nihon Eiseigaku Zasshi] 2015; Vol. 70 (3), pp. 186-96. |
| DOI: |
10.1265/jjh.70.186 |
| Abstrakt: |
Arsenic metabolism affects the susceptibility of humans to arsenic toxicity; therefore, clarification of the factors associated with individual variations in arsenic metabolism is an important task. Genetic polymorphisms such as single nucleotide polymorphisms (SNPs) in arsenic (+3 oxidation state) methyltransferase (AS3MT), which can methylate arsenic compounds using S-adenosyl-l-methionine (AdoMet), have been reported to modify arsenic methylation. In this review, we summarize studies conducted by us in Vietnam and by others on the association of AS3MT genetic polymorphisms with arsenic metabolism as well as human health effects. Most of the SNPs in AS3MT showed inconsistent results in terms of genotype-dependent differences in arsenic metabolism among the studies. However, AS3MT 12390 (rs3740393) and 14458 (rs11191439) were consistently related to arsenic methylation regardless of the study population: AS3MT 12390 (rs3740393) affected the second step of methylation of arsenic, whereas 14458 (rs11191439) affected the first methylation step. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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