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Hazard identification: efficiency of short-term tests in identifying germ cell mutagens and putative nongenotoxic carcinogens.

机译:危害识别:识别生殖细胞诱变剂和推定的非遗传毒性致癌物的短期测试的效率。

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摘要

For more than a decade, mutagenicity tests have had a clearly defined role in the identification of potential human mutagens and an ancillary role in the identification of potential human carcinogens. The efficiency of short-term tests in identifying germ cell mutagens has been examined using a combined data set derived from the U.S. Environmental Protection Agency/International Agency for Research on Cancer Genetic Activity Profile (EPA/IARC GAP) and EPA Gene-Tox databases. Our review of these data indicates adequate sensitivity of batteries of in vitro short-term mutagenicity tests in identifying germ cell mutagens. The analysis also supports the inclusion of an in vivo assay as suggested in proposed regulatory testing guidelines. In the context of carcinogenicity testing, the ability of short-term bioassays to detect genotoxic or mutagenic carcinogens is well established. Such tests are not considered to be as sensitive to nongenotoxic or nonmutagenic carcinogens. However, analyses presented in this report using the EPA/IARC GAP database demonstrate that many putative nongenotoxic carcinogens that have been adequately tested in short-term genetic bioassays induce gene or chromosomal mutation or aneuploidy. Further investigation should reveal whether the mutagenicity of these agents plays an important mechanistic role in their carcinogenicity.
机译:十多年来,致突变性测试在鉴定潜在的人类诱变剂中具有明确定义的作用,在鉴定潜在的人类致癌物方面具有辅助作用。已经使用美国环境保护署/国际癌症遗传活性谱研究机构(EPA / IARC GAP)和EPA Gene-Tox数据库的组合数据集对鉴定生殖细胞诱变剂的短期测试的效率进行了检查。我们对这些数据的审查表明,体外短期致突变性测试对鉴定生殖细胞诱变剂具有足够的敏感性。该分析还支持提议的监管测试指南中建议的体内分析。在致癌性测试的背景下,已经建立了短期生物测定法检测遗传毒性或致突变性致癌物的能力。此类测试不被视为对非遗传毒性或非诱变致癌物敏感。但是,本报告中使用EPA / IARC GAP数据库进行的分析表明,已在短期遗传生物测定法中经过充分测试的许多假定的非遗传毒性致癌物均会诱导基因或染色体突变或非整倍性。进一步的研究应揭示这些试剂的致突变性是否在其致癌性中起重要的机械作用。

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