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丙烯酰胺的遗传毒性评估。

Assessment of the genotoxicity of acrylamide.

作者信息

Benford Diane, Bignami Margherita, Chipman James Kevin, Ramos Bordajandi Luisa

出版信息

EFSA J. 2022 May 5;20(5):e07293. doi: 10.2903/j.efsa.2022.7293. eCollection 2022 May.

Abstract

EFSA was requested to deliver a statement on a recent publication revisiting the evidence for genotoxicity of acrylamide (AA). The statement was prepared by a Working Group and was endorsed by the CONTAM Panel before its final approval. In interpreting the Terms of Reference, the statement considered the modes of action underlying the carcinogenicity of AA including genotoxic and non-genotoxic effects. Relevant publications since the 2015 CONTAM Panel Opinion on AA in food were reviewed. Several new studies reported positive results on the clastogenic and mutagenic properties of AA and its active metabolite glycidamide (GA). DNA adducts of GA were induced by AA exposure in experimental animals and have also been observed in humans. In addition to the genotoxicity of AA, there is evidence for both secondary DNA oxidation via generation of reactive oxygen species and for non-genotoxic effects which may contribute to carcinogenesis by AA. These studies extend the information assessed by the CONTAM Panel in its 2015 Opinion, and support its conclusions. That Opinion applied the margin of exposure (MOE) approach, as recommended in the EFSA Guidance for substances that are both genotoxic and carcinogenic, for risk characterisation of the neoplastic effects of AA. Based on the new data evaluated, the MOE approach is still considered appropriate, and an update of the 2015 Opinion is not required at the present time.

摘要

欧洲食品安全局(EFSA)被要求就最近一篇重新审视丙烯酰胺(AA)遗传毒性证据的出版物发表声明。该声明由一个工作组编写,并在最终批准前得到了食品链污染物专家小组(CONTAM Panel)的认可。在解释职权范围时,该声明考虑了AA致癌性的作用模式,包括遗传毒性和非遗传毒性作用。对自2015年CONTAM小组关于食品中AA的意见以来的相关出版物进行了审查。几项新研究报告了AA及其活性代谢物环氧丙酰胺(GA)的致断裂和致突变特性的阳性结果。在实验动物中,AA暴露可诱导GA的DNA加合物,在人类中也观察到了这种加合物。除了AA的遗传毒性外,有证据表明通过产生活性氧导致继发性DNA氧化,以及存在可能导致AA致癌的非遗传毒性作用。这些研究扩展了CONTAM小组在其2015年意见中评估的信息,并支持其结论。该意见采用了暴露边际(MOE)方法,正如EFSA对具有遗传毒性和致癌性物质的指南中所建议的那样,用于对AA的肿瘤效应进行风险特征描述。基于评估的新数据,MOE方法仍然被认为是合适的,目前不需要更新2015年的意见。

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