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Synergy between systemic toxicity and genotoxicity: relevance to human cancer risk.

机译:全身毒性和遗传毒性之间的协同作用:与人类癌症风险的相关性。

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摘要

The health risk manager and policy analyst must frequently make recommendations based upon incomplete toxicity data. This is a situation which is encountered in the evaluation of human carcinogenic risks as animal cancer bioassay results are often not available. In this study, in order to assess the relevance of other possible indicators of carcinogenic risks, we used the "chemical diversity approach" to estimate the magnitude of the human carcinogenic risk based upon Salmonella mutagenicity and systemic toxicity data of the "universe of chemicals" to which humans have the potential to be exposed. Analyses of the properties of 10,000 agents representative of the "universe of chemicals" suggest that chemicals that have genotoxic potentials as well as exhibiting greater systemic toxicity are more likely to be carcinogens than non-genotoxicants or agents that exhibit lesser toxicity. Since "genotoxic" carcinogenicity is a hallmark of recognized human carcinogens, these findings are relevant to human cancer risk assessment.
机译:健康风险经理和政策分析师必须经常根据不完全的毒性数据提出建议。由于通常无法获得动物癌症的生物测定结果,因此在评估人类致癌风险时会遇到这种情况。在这项研究中,为了评估其他可能的致癌风险指标的相关性,我们使用了“化学多样性方法”,根据沙门氏菌的致突变性和“化学品宇宙”的系统毒性数据,估计了人类致癌风险的大小。人类可能会接触到的潜力。对代表“化学物质宇宙”的10,000种药物的特性进行的分析表明,与具有非遗传毒性的药物或毒性较小的药物相比,具有遗传毒性的潜力以及表现出更大的系统毒性的化学物质更可能是致癌物。由于“遗传毒性”致癌性是公认的人类致癌物的标志,因此这些发现与人类癌症风险评估有关。

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