Toenail arsenic species and metallome profiles associated with breast, cervical, prostate, and skin cancer prevalence in the Atlantic Partnership for Tomorrow’s Health cohort

前列腺癌 队列 医学 乳腺癌 宫颈癌 癌症 肿瘤科 内科学 入射(几何) 环境卫生 生理学 妇科 化学 物理 有机化学 光学
作者
Kalli Hood,Ellen Sweeney,Gabriela Ilie,Erin Keltie,Jong Sung Kim
出处
期刊:Frontiers in Public Health [Frontiers Media SA]
卷期号:11 被引量:2
标识
DOI:10.3389/fpubh.2023.1148283
摘要

Introduction Chronic exposure to arsenic through drinking water has been linked to several cancers. The metabolism of arsenic is thought to play a key role in arsenic-related carcinogenesis as metabolites of varying toxicity are produced and either stored in or excreted from the body. Atlantic Canada has the highest age-standardized incidence rates of all cancers in the country. This may be due to its high levels of environmental arsenic and the prevalence of unregulated private wells for water consumption. Here, we aimed to characterize the profiles of arsenic species and metallome in the toenails of four cancer groups, compare them to healthy participants ( N = 338), and assess potential associations between the profiles with cancer prevalence. Methods This study employed a case–control design. Toenail samples and questionnaire data from cases (breast, cervical, prostate, and skin cancers) and controls were sourced from the Atlantic Partnership for Tomorrow’s Health (PATH) cohort study. The levels of arsenic species were measured using Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) paired with High Performance Liquid Chromatography (HPLC) and total concentrations of metallome (23 metals) were determined by ICP-MS separately. Multivariate analyses were conducted to compare cases with controls within each cancer group. Results Arsenic speciation profiles varied by cancer type and were significantly different between cases and controls in the breast ( p = 0.0330), cervical ( p = 0.0228), and skin ( p = 0.0228) cancer groups. In addition, the profiles of metallome (nine metals) were significantly differentiated in the prostate ( p = 0.0244) and skin ( p = 0.0321) cancer groups, with higher zinc concentrations among cases compared to controls. Conclusion History of cancer diagnosis was associated with specific profiles of arsenic species and metallome. Our results indicate that arsenic methylation and zinc levels, as measured in toenails, may be an important biomarker for cancer prevalence. Further research is needed to use toenails as a prognostic measure of arsenic-and other metal-induced cancer.

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