砷的协同致癌作用:抑制 DNA 修复和与锌指蛋白的相互作用。

Arsenic co-carcinogenesis: Inhibition of DNA repair and interaction with zinc finger proteins.

机构信息

Department of Pharmaceutical Sciences, University of New Mexico Health Sciences Center, Albuquerque, NM, 87131, USA.

Department of Pharmaceutical Sciences, University of New Mexico Health Sciences Center, Albuquerque, NM, 87131, USA.

出版信息

Semin Cancer Biol. 2021 Nov;76:86-98. doi: 10.1016/j.semcancer.2021.05.009. Epub 2021 May 10.

Abstract

Arsenic is widely present in the environment and is associated with various population health risks including cancers. Arsenic exposure at environmentally relevant levels enhances the mutagenic effect of other carcinogens such as ultraviolet radiation. Investigation on the molecular mechanisms could inform the prevention and intervention strategies of arsenic carcinogenesis and co-carcinogenesis. Arsenic inhibition of DNA repair has been demonstrated to be an important mechanism, and certain DNA repair proteins have been identified to be extremely sensitive to arsenic exposure. This review will summarize the recent advances in understanding the mechanisms of arsenic carcinogenesis and co-carcinogenesis, including DNA damage induction and ROS generation, particularly how arsenic inhibits DNA repair through an integrated molecular mechanism which includes its interactions with sensitive zinc finger DNA repair proteins.

摘要

砷广泛存在于环境中,与包括癌症在内的各种人群健康风险有关。在与环境相关的水平下暴露于砷会增强其他致癌物(如紫外线辐射)的致突变作用。对分子机制的研究可以为预防和干预砷致癌和协同致癌提供信息。已经证明,砷抑制 DNA 修复是一个重要的机制,并且已经确定某些 DNA 修复蛋白对砷暴露极其敏感。本综述将总结近年来对砷致癌和协同致癌机制的理解进展,包括 DNA 损伤诱导和 ROS 生成,特别是砷如何通过包括与敏感锌指 DNA 修复蛋白相互作用在内的综合分子机制来抑制 DNA 修复。

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