Mutagens and Sensitizers—An Unequal Relationship?

A. Wolfreys, D. Basketter
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引用次数: 8

Abstract

For some years, those involved with the safety assessment of chemicals have in one way or another considered the degree to which data on either skin sensitization potential or on carcinogenicity may inform them on the other endpoint for a particular substance. In this work, we have taken a pragmatic perspective on the question and assessed mutagens, rather than carcinogens, and sensitizers as this better reflects the potential for biological macromolecule interaction. A dataset of 100 substances, the majority of which have come under scrutiny for one reason or another during our own toxicology investigations, was interrogated. We focused on the extent to which results from the primary screen for skin sensitization correlated with the results from the two in vitro tests used as a screen for mutagenicity, namely the bacterial mutation assay and the in vitro chromosome aberration assay. Although there was some concordance between the two endpoints, as standalone methods, neither predicted the other particularly accurately, with 32% showing disagreement. It is probable that there are several critical elements missing from this top level assessment, not least an appreciation of which substances are positive in mutagenicity tests via non‐genotoxic mechanisms which could seriously impair such a correlation between results from the two different endpoints.
诱变剂和致敏剂——不平等关系?
多年来,那些参与化学品安全评估的人以这样或那样的方式考虑了皮肤致敏潜力或致癌性数据的程度,这些数据可能会告诉他们某种特定物质的另一个终点。在这项工作中,我们对这个问题采取了务实的观点,并评估了诱变剂,而不是致癌物和致敏剂,因为这更好地反映了生物大分子相互作用的潜力。我们查阅了100种物质的数据集,其中大部分在我们自己的毒理学调查中由于这样或那样的原因受到了审查。我们关注的是皮肤致敏初级筛查结果与两项用于致突变性筛查的体外试验(即细菌突变试验和体外染色体畸变试验)结果的相关性。虽然两个终点之间有一些一致性,作为独立的方法,没有一个预测对方特别准确,有32%的人表示不一致。这一顶级评估可能缺少几个关键因素,尤其是没有认识到哪些物质在通过非基因毒性机制进行的致突变性试验中呈阳性,这可能严重损害两个不同终点结果之间的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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