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更新的甲醛相关鼻肿瘤作用模式和人类相关性框架评估

An updated mode of action and human relevance framework evaluation for Formaldehyde-Related nasal tumors.

机构信息

ToxStrategies, Inc, Katy, TX, USA.

Ramboll, Monroe, LA, USA.

出版信息

Crit Rev Toxicol. 2020 Nov;50(10):919-952. doi: 10.1080/10408444.2020.1854679.

Abstract

Formaldehyde is a reactive aldehyde naturally present in all plant and animal tissues and a critical component of the one-carbon metabolism pathway. It is also a high production volume chemical used in the manufacture of numerous products. Formaldehyde is also one of the most well-studied chemicals with respect to environmental fate, biology, and toxicology-including carcinogenic potential, and mode of action (MOA). In 2006, a published MOA for formaldehyde-induced nasal tumors in rats concluded that nasal tumors were most likely driven by cytotoxicity and regenerative cell proliferation, with possible contributions from direct genotoxicity. In the past 15 years, new research has better informed the MOA with the publication of genotoxicity assays, toxicogenomic analyses, and development of ultra-sensitive methods to measure endogenous and exogenous formaldehyde-induced DNA adducts. Herein, we review and update the MOA for nasal tumors, with particular emphasis on the numerous studies published since 2006. These new studies further underscore the involvement of cytotoxicity and regenerative cell proliferation, and further inform the genotoxic potential of inhaled formaldehyde. The data lend additional support for the use of mechanistic data for the derivation of toxicity criteria and/or scientifically supported approaches for low-dose extrapolation for the risk assessment of formaldehyde.

摘要

甲醛是一种存在于所有动植物组织中的反应性醛类物质,也是一碳代谢途径的关键组成部分。它也是一种高产量的化学物质,用于制造众多产品。甲醛也是环境归宿、生物学和毒理学(包括致癌潜力和作用模式)方面研究最充分的化学物质之一。2006 年,发表的甲醛诱导大鼠鼻腔肿瘤的作用模式研究结论认为,鼻腔肿瘤最有可能是由细胞毒性和再生细胞增殖驱动的,直接遗传毒性可能也有一定作用。在过去的 15 年中,随着遗传毒性检测、毒理基因组学分析以及测量内源性和外源性甲醛诱导的 DNA 加合物的超灵敏方法的发展,新的研究为作用模式提供了更好的信息。本文综述并更新了鼻腔肿瘤的作用模式,特别强调了自 2006 年以来发表的大量研究。这些新研究进一步强调了细胞毒性和再生细胞增殖的作用,并进一步阐明了吸入甲醛的遗传毒性潜力。这些数据为使用机制数据推导毒性标准以及/或科学支持的低剂量外推方法来评估甲醛风险提供了额外的支持。

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