PMID- 33905762 OWN - NLM STAT- MEDLINE DCOM- 20210622 LR - 20231107 IS - 1879-3185 (Electronic) IS - 0300-483X (Print) IS - 0300-483X (Linking) VI - 457 DP - 2021 Jun 15 TI - Nutrition, one-carbon metabolism and arsenic methylation. PG - 152803 LID - S0300-483X(21)00126-8 [pii] LID - 10.1016/j.tox.2021.152803 [doi] AB - Exposure to arsenic (As) is a major public health concern globally. Inorganic As (InAs) undergoes hepatic methylation to form monomethyl (MMAs)- and dimethyl (DMAs)-arsenical species, facilitating urinary As elimination. MMAs(III) is considerably more toxic than either InAs(III) or DMAs(V), and a higher proportion of MMAs in urine has been associated with risk for a wide range of adverse health outcomes. Efficiency of As methylation differs substantially between species, between individuals, and across populations. One-carbon metabolism (OCM) is a biochemical pathway that provides methyl groups for the methylation of As, and is influenced by folate and other micronutrients, such as vitamin B(12), choline, betaine and creatine. A growing body of evidence has demonstrated that OCM-related micronutrients play a critical role in As methylation. This review will summarize observational epidemiological studies, interventions, and relevant experimental evidence examining the role that OCM-related micronutrients have on As methylation, toxicity of As, and risk for associated adverse health-related outcomes. There is fairly robust evidence supporting the impact of folate on As methylation, and some evidence from case-control studies indicating that folate nutritional status influences risk for As-induced skin lesions and bladder cancer. However, the potential for folate to be protective for other As-related health outcomes, and the potential beneficial effects of other OCM-related micronutrients on As methylation and risk for health outcomes are less well studied and warrant additional research. CI - Copyright (c) 2021 Elsevier B.V. All rights reserved. FAU - Abuawad, Ahlam AU - Abuawad A AD - Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, USA. FAU - Bozack, Anne K AU - Bozack AK AD - Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, USA; Division of Environmental Health Sciences, School of Public Health, University of California, Berkeley, CA, USA. FAU - Saxena, Roheeni AU - Saxena R AD - Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, USA. FAU - Gamble, Mary V AU - Gamble MV AD - Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, USA. Electronic address: mvg7@cumc.columbia.edu. LA - eng GR - R01 ES030945/ES/NIEHS NIH HHS/United States GR - P42 ES010349/ES/NIEHS NIH HHS/United States GR - F31 ES032321/ES/NIEHS NIH HHS/United States GR - R25 GM062454/GM/NIGMS NIH HHS/United States GR - P30 ES009089/ES/NIEHS NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PT - Review DEP - 20210424 PL - Ireland TA - Toxicology JT - Toxicology JID - 0361055 RN - 0 (Drinking Water) RN - 7440-44-0 (Carbon) RN - 935E97BOY8 (Folic Acid) RN - N712M78A8G (Arsenic) SB - IM MH - Animals MH - Arsenic/*metabolism/toxicity MH - Carbon/*metabolism MH - Drinking Water/adverse effects/metabolism MH - Environmental Exposure/*adverse effects MH - Female MH - Folic Acid/administration & dosage MH - Folic Acid Deficiency/diet therapy/epidemiology/metabolism MH - Food/toxicity MH - Humans MH - Methylation MH - Nutritional Status/drug effects/*physiology MH - Observational Studies as Topic/methods MH - Pregnancy MH - Prenatal Exposure Delayed Effects/chemically induced/epidemiology/metabolism PMC - PMC8349595 MID - NIHMS1697218 OTO - NOTNLM OT - Arsenic OT - Arsenic methylation OT - Folate OT - Nutrition OT - One-carbon metabolism COIS- Declaration of interests The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. EDAT- 2021/04/28 06:00 MHDA- 2021/06/23 06:00 PMCR- 2022/06/15 CRDT- 2021/04/27 20:10 PHST- 2020/12/23 00:00 [received] PHST- 2021/04/20 00:00 [revised] PHST- 2021/04/22 00:00 [accepted] PHST- 2021/04/28 06:00 [pubmed] PHST- 2021/06/23 06:00 [medline] PHST- 2021/04/27 20:10 [entrez] PHST- 2022/06/15 00:00 [pmc-release] AID - S0300-483X(21)00126-8 [pii] AID - 10.1016/j.tox.2021.152803 [doi] PST - ppublish SO - Toxicology. 2021 Jun 15;457:152803. doi: 10.1016/j.tox.2021.152803. Epub 2021 Apr 24.