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Title: Individual differences in arsenic metabolism and lung cancer in a case-control study in Cordoba, Argentina

Journal Article · · Toxicology and Applied Pharmacology
 [1];  [2];  [3];  [4]; ; ; ; ; ; ; ;  [2]
  1. Office of Environmental Health Hazard Assessment, California Environmental Protection Agency, Oakland, CA (United States)
  2. School of Public Health, University of California, Berkeley, CA (United States)
  3. School of Public Health and Community Medicine, University of Washington, Seattle, WA (United States)
  4. Facultad de Medicina, Universidad Catolica de Cordoba, Cordoba (Argentina)

In humans, ingested inorganic arsenic is metabolized to monomethylarsenic (MMA) then to dimethylarsenic (DMA), although in most people this process is not complete. Previous studies have identified associations between the proportion of urinary MMA (%MMA) and increased risks of several arsenic-related diseases, although none of these reported on lung cancer. In this study, urinary arsenic metabolites were assessed in 45 lung cancer cases and 75 controls from arsenic-exposed areas in Cordoba, Argentina. Folate has also been linked to arsenic-disease susceptibility, thus an exploratory assessment of associations between single nucleotide polymorphisms in folate metabolizing genes, arsenic methylation, and lung cancer was also conducted. In analyses limited to subjects with metabolite concentrations above detection limits, the mean %MMA was higher in cases than in controls (17.5% versus 14.3%, p = 0.01). The lung cancer odds ratio for subjects with %MMA in the upper tertile compared to those in the lowest tertile was 3.09 (95% CI, 1.08-8.81). Although the study size was too small for a definitive conclusion, there was an indication that lung cancer risks might be highest in those with a high %MMA who also carried cystathionine {beta}-synthase (CBS) rs234709 and rs4920037 variant alleles. This study is the first to report an association between individual differences in arsenic metabolism and lung cancer, a leading cause of arsenic-related mortality. These results add to the increasing body of evidence that variation in arsenic metabolism plays an important role in arsenic-disease susceptibility.

OSTI ID:
21451182
Journal Information:
Toxicology and Applied Pharmacology, Vol. 247, Issue 2; Other Information: DOI: 10.1016/j.taap.2010.06.006; PII: S0041-008X(10)00200-0; Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; ISSN 0041-008X
Country of Publication:
United States
Language:
English