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遗传毒性评估:运用最佳科学方法进行人体安全性评估 第七部分:为何不先从单一测试开始:遗传毒性危害与风险评估的变革性替代方法

Genetic toxicity assessment: employing the best science for human safety evaluation Part VII: Why not start with a single test: a transformational alternative to genotoxicity hazard and risk assessment.

作者信息

Ku Warren W, Aubrecht Jiri, Mauthe Robert J, Schiestl Robert H, Fornace Albert J

机构信息

Exploratory Medicinal Sciences, Pfizer Global Research and Development, Groton, CT 06340, USA.

出版信息

Toxicol Sci. 2007 Sep;99(1):20-5. doi: 10.1093/toxsci/kfm147. Epub 2007 Jun 4.

Abstract

A transformational alternative for genotoxicity hazard and risk assessment is proposed to the current standard regulatory test battery. In principle, the proposed approach consists of a single in vitro test system with high genomic sequence homology to humans that addresses the relevant principal genetic lesions assessed in the current test battery. The single test system also possesses higher throughput attributes to permit the screening of large numbers of compounds and allow for an initial differentiation of genotoxic mechanisms (i.e., direct vs. indirect mechanisms) by how the hazard end point is measured. To differentiate compounds showing positive results, toxicogenomic analysis can be conducted to evaluate genotoxic mechanisms and further support risk assessment. Lastly, the results from the single test system can be followed up with a complementary in vivo assessment to establish mechanistic relevance at potential target tissues. Here, we propose the in vitro (yeast) DNA deletion (DEL) recombination assay as a single test alternative to the current genotoxicity test battery with a mechanistic follow up toxicogenomic analysis of genotoxic stress response as one approach that requires broader evaluation and validation. In this assay, intrachromosomal recombination events between a repeated DNA sequence lead to DNA deletions, which have been shown to be inducible by a variety of carcinogens including those both negative and positive in the standard Salmonella Ames assay. It is hoped that the general framework outlined along with this specific example will provoke broader interest to propose other potential test systems.

摘要

针对目前标准的监管测试组合,提出了一种用于遗传毒性危害和风险评估的变革性替代方法。原则上,所提出的方法包括一个与人类具有高度基因组序列同源性的单一体外测试系统,该系统可解决当前测试组合中评估的相关主要遗传损伤问题。该单一测试系统还具有更高的通量属性,以允许筛选大量化合物,并通过测量危害终点的方式对遗传毒性机制(即直接机制与间接机制)进行初步区分。为了区分显示阳性结果的化合物,可以进行毒理基因组分析以评估遗传毒性机制并进一步支持风险评估。最后,单一测试系统的结果可以通过补充的体内评估进行跟进,以确定在潜在靶组织中的机制相关性。在此,我们提出体外(酵母)DNA缺失(DEL)重组试验作为当前遗传毒性测试组合的单一测试替代方法,并将遗传毒性应激反应的机制性后续毒理基因组分析作为一种需要更广泛评估和验证的方法。在该试验中,重复DNA序列之间的染色体内重组事件会导致DNA缺失,已证明多种致癌物可诱导这种缺失,包括在标准沙门氏菌艾姆斯试验中呈阴性和阳性的致癌物。希望连同这个具体例子概述的总体框架能引发更广泛的兴趣,以提出其他潜在的测试系统。

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