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国际癌症研究机构将氧化应激用作促进癌症分类的关键作用模式特征:草甘膦案例说明了解释性实施中缺乏稳健性。

IARC use of oxidative stress as key mode of action characteristic for facilitating cancer classification: Glyphosate case example illustrating a lack of robustness in interpretative implementation.

作者信息

Bus James S

机构信息

Exponent, Inc., 1800 Diagonal Road, Suite 500, Alexandria, VA 22314, United States.

出版信息

Regul Toxicol Pharmacol. 2017 Jun;86:157-166. doi: 10.1016/j.yrtph.2017.03.004. Epub 2017 Mar 6.

Abstract

The International Agency for Research on Cancer (IARC) has formulated 10 key characteristics of human carcinogens to incorporate mechanistic data into cancer hazard classifications. The analysis used glyphosate as a case example to examine the robustness of IARC's determination of oxidative stress as "strong" evidence supporting a plausible cancer mechanism in humans. The IARC analysis primarily relied on 14 human/mammalian studies; 19 non-mammalian studies were uninformative of human cancer given the broad spectrum of test species and extensive use of formulations and aquatic testing. The mammalian studies had substantial experimental limitations for informing cancer mechanism including use of: single doses and time points; cytotoxic/toxic test doses; tissues not identified as potential cancer targets; glyphosate formulations or mixtures; technically limited oxidative stress biomarkers. The doses were many orders of magnitude higher than human exposures determined in human biomonitoring studies. The glyphosate case example reveals that the IARC evaluation fell substantially short of "strong" supporting evidence of oxidative stress as a plausible human cancer mechanism, and suggests that other IARC monographs relying on the 10 key characteristics approach should be similarly examined for a lack of robust data integration fundamental to reasonable mode of action evaluations.

摘要

国际癌症研究机构(IARC)已制定了人类致癌物的10个关键特征,以便将机制数据纳入癌症风险分类。该分析以草甘膦为例,检验了IARC将氧化应激确定为支持人类可能致癌机制的“有力”证据的稳健性。IARC的分析主要依赖于14项人类/哺乳动物研究;鉴于测试物种范围广泛以及制剂的广泛使用和水生测试,19项非哺乳动物研究对人类癌症并无参考价值。这些哺乳动物研究在为癌症机制提供信息方面存在重大实验局限性,包括使用:单剂量和时间点;细胞毒性/毒性测试剂量;未被确定为潜在癌症靶点的组织;草甘膦制剂或混合物;技术上有限的氧化应激生物标志物。这些剂量比人类生物监测研究确定的人类接触剂量高出许多个数量级。草甘膦的案例表明,IARC的评估远远缺乏将氧化应激作为一种合理的人类癌症机制的确凿支持证据,并表明其他依赖10个关键特征方法的IARC专论也应同样接受审查,看是否缺乏合理作用模式评估所必需的稳健数据整合。

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