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Environmental arsenic exposure: From genetic susceptibility to pathogenesis

机译:环境砷暴露:从遗传易感性到发病机理

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摘要

More than 200 million people in 70 countries are exposed to arsenic through drinking water. Chronic exposure to this metalloid has been associated with the onset of many diseases, including cancer. Epidemiological evidence supports its carcinogenic potential, however, detailed molecular mechanisms remain to be elucidated. Despite the global magnitude of this problem, not all individuals face the same risk. Susceptibility to the toxic effects of arsenic is influenced by alterations in genes involved in arsenic metabolism, as well as biological factors, such as age, gender and nutrition. Moreover, chronic arsenic exposure results in several genotoxic and epigenetic alterations tightly associated with the arsenic biotransformation process, resulting in an increased cancer risk. In this review, we: 1) review the roles of inter-individual DNA-level variations influencing the susceptibility to arsenic-induced carcinogenesis; 2) discuss the contribution of arsenic biotransformation to cancer initiation; 3) provide insights into emerging research areas and the challenges in the field; and 4) compile a resource of publicly available arsenic-related DNA-level variations, transcriptome and methylation data. Understanding the molecular mechanisms of arsenic exposure and its subsequent health effects will support efforts to reduce the worldwide health burden and encourage the development of strategies for managing arsenic-related diseases in the era of personalized medicine.
机译:70个国家/地区的2亿多人通过饮用水接触砷。长期暴露于这种准金属与许多疾病的发作有关,包括癌症。流行病学证据支持其致癌潜力,但是,尚需阐明详细的分子机制。尽管此问题在全球范围内都存在,但并非所有人都面临相同的风险。砷毒性作用的易感性受砷代谢相关基因的改变以及年龄,性别和营养等生物学因素的影响。此外,慢性砷暴露导致与砷生物转化过程紧密相关的多种遗传毒性和表观遗传学改变,从而增加了患癌症的风险。在这篇综述中,我们:1)综述个体间DNA水平变异对砷诱导的致癌性敏感性的影响; 2)讨论砷生物转化对癌症引发的贡献; 3)提供有关新兴研究领域和该领域挑战的见解;和4)汇编公开的砷相关DNA水平变异,转录组和甲基化数据的资源。了解砷暴露的分子机制及其对健康的影响,将有助于减少全球健康负担的努力,并鼓励制定个性化医学时代用于管理砷相关疾病的策略。

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