Zeiger Errol, Gollapudi Bhaskar, Aardema Marilyn J, Auerbach Scott, Boverhof Darrell, Custer Laura, Dedon Peter, Honma Masamitsu, Ishida Seiichi, Kasinski Andrea L, Kim James H, Manjanatha Mugimane G, Marlowe Jennifer, Pfuhler Stefan, Pogribny Igor, Slikker William, Stankowski Leon F, Tanir Jennifer Y, Tice Raymond, van Benthem Jan, White Paul, Witt Kristine L, Thybaud Véronique
Errol Zeiger Consulting, Chapel Hill, North Carolina.
Environ Mol Mutagen. 2015 Apr;56(3):277-85. doi: 10.1002/em.21923. Epub 2014 Dec 6.
Genetic toxicity tests currently used to identify and characterize potential human mutagens and carcinogens rely on measurements of primary DNA damage, gene mutation, and chromosome damage in vitro and in rodents. The International Life Sciences Institute Health and Environmental Sciences Institute (ILSI-HESI) Committee on the Relevance and Follow-up of Positive Results in In Vitro Genetic Toxicity Testing held an April 2012 Workshop in Washington, DC, to consider the impact of new understanding of biology and new technologies on the identification and characterization of genotoxic substances, and to identify new approaches to inform more accurate human risk assessment for genetic and carcinogenic effects. Workshop organizers and speakers were from industry, academe, and government. The Workshop focused on biological effects and technologies that would potentially yield the most useful information for evaluating human risk of genetic damage. Also addressed was the impact that improved understanding of biology and availability of new techniques might have on genetic toxicology practices. Workshop topics included (1) alternative experimental models to improve genetic toxicity testing, (2) Biomarkers of epigenetic changes and their applicability to genetic toxicology, and (3) new technologies and approaches. The ability of these new tests and technologies to be developed into tests to identify and characterize genotoxic agents; to serve as a bridge between in vitro and in vivo rodent, or preferably human, data; or to be used to provide dose response information for quantitative risk assessment was also addressed. A summary of the workshop and links to the scientific presentations are provided.
目前用于识别和表征潜在人类诱变剂和致癌物的遗传毒性测试依赖于在体外和啮齿动物体内对原发性DNA损伤、基因突变和染色体损伤的测量。国际生命科学研究所健康与环境科学研究所(ILSI-HESI)体外遗传毒性测试阳性结果的相关性及后续跟进委员会于2012年4月在华盛顿特区举办了一次研讨会,以探讨生物学新认识和新技术对遗传毒性物质识别与表征的影响,并确定新方法,为更准确的人类遗传和致癌效应风险评估提供依据。研讨会的组织者和发言者来自行业、学术界和政府。该研讨会聚焦于可能为评估人类遗传损伤风险产生最有用信息的生物学效应和技术。还讨论了对生物学理解的加深和新技术的可用性可能对遗传毒理学实践产生的影响。研讨会主题包括:(1)改进遗传毒性测试的替代实验模型;(2)表观遗传变化的生物标志物及其在遗传毒理学中的适用性;(3)新技术和新方法。还讨论了这些新测试和技术能否发展成为识别和表征遗传毒性剂的测试;能否作为体外和体内啮齿动物(或更理想的是人类)数据之间的桥梁;或能否用于提供剂量反应信息以进行定量风险评估。本文提供了研讨会总结以及科学报告的链接。