• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1093/toxsci/kfm147
PMID:17548889
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。

相似文献

1
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.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
Toxicol Sci. 2007 Sep;99(1):20-5. doi: 10.1093/toxsci/kfm147. Epub 2007 Jun 4.
2
Strategy for genotoxicity testing: hazard identification and risk assessment in relation to in vitro testing.遗传毒性测试策略:与体外测试相关的危害识别和风险评估
Mutat Res. 2007 Feb 3;627(1):41-58. doi: 10.1016/j.mrgentox.2006.10.003. Epub 2006 Nov 27.
3
Genetic toxicity assessment: employing the best science for human safety evaluation part IV: Recommendation of a working group of the Gesellschaft fuer Umwelt-Mutationsforschung (GUM) for a simple and straightforward approach to genotoxicity testing.遗传毒性评估:运用最佳科学方法进行人体安全性评估 第四部分:环境突变研究协会(GUM)一个工作组关于遗传毒性测试简单直接方法的建议
Toxicol Sci. 2007 Jun;97(2):237-40. doi: 10.1093/toxsci/kfm019. Epub 2007 Feb 14.
4
Strategy for genotoxicity testing--metabolic considerations.遗传毒性测试策略——代谢方面的考虑因素。
Mutat Res. 2007 Feb 3;627(1):59-77. doi: 10.1016/j.mrgentox.2006.10.004. Epub 2006 Dec 1.
5
Evaluation of the ability of a battery of three in vitro genotoxicity tests to discriminate rodent carcinogens and non-carcinogens I. Sensitivity, specificity and relative predictivity.一组三项体外遗传毒性试验鉴别啮齿动物致癌物和非致癌物能力的评估I. 敏感性、特异性和相对预测性
Mutat Res. 2005 Jul 4;584(1-2):1-256. doi: 10.1016/j.mrgentox.2005.02.004.
6
How to assess the mutagenic potential of cosmetic products without animal tests?如何在不进行动物试验的情况下评估化妆品的致突变潜力?
Mutat Res. 2009 Aug;678(2):108-12. doi: 10.1016/j.mrgentox.2009.04.006. Epub 2009 Apr 18.
7
Testing strategies in mutagenicity and genetic toxicology: an appraisal of the guidelines of the European Scientific Committee for Cosmetics and Non-Food Products for the evaluation of hair dyes.致突变性和遗传毒理学中的测试策略:对欧洲化妆品和非食品产品科学委员会染发剂评估指南的评价。
Mutat Res. 2005 Dec 30;588(2):88-105. doi: 10.1016/j.mrgentox.2005.09.006. Epub 2005 Dec 2.
8
Safety and nutritional assessment of GM plants and derived food and feed: the role of animal feeding trials.转基因植物及其衍生食品和饲料的安全性与营养评估:动物饲养试验的作用
Food Chem Toxicol. 2008 Mar;46 Suppl 1:S2-70. doi: 10.1016/j.fct.2008.02.008. Epub 2008 Feb 13.
9
Evaluation of the ability of a battery of three in vitro genotoxicity tests to discriminate rodent carcinogens and non-carcinogens II. Further analysis of mammalian cell results, relative predictivity and tumour profiles.一组三项体外遗传毒性试验鉴别啮齿类致癌物和非致癌物能力的评估II. 哺乳动物细胞结果、相对预测性及肿瘤谱的进一步分析
Mutat Res. 2006 Sep 19;608(1):29-42. doi: 10.1016/j.mrgentox.2006.04.017.
10
Development of genotoxicity test procedures with Episkin, a reconstructed human skin model: towards new tools for in vitro risk assessment of dermally applied compounds?使用重组人皮模型Episkin开发遗传毒性测试程序:能否成为用于经皮应用化合物体外风险评估的新工具?
Mutat Res. 2006 Jul 14;606(1-2):39-51. doi: 10.1016/j.mrgentox.2006.02.009. Epub 2006 May 3.

引用本文的文献

1
Development and validation of a high-throughput transcriptomic biomarker to address 21st century genetic toxicology needs.开发和验证高通量转录组生物标志物以满足 21 世纪遗传毒理学的需求。
Proc Natl Acad Sci U S A. 2017 Dec 19;114(51):E10881-E10889. doi: 10.1073/pnas.1714109114. Epub 2017 Dec 4.
2
Radiation metabolomics and its potential in biodosimetry.辐射代谢组学及其在生物剂量学中的潜力。
Int J Radiat Biol. 2011 Aug;87(8):802-23. doi: 10.3109/09553002.2011.556177. Epub 2011 Jun 22.
3
Yeast DEL assay detects protection against radiation-induced cytotoxicity and genotoxicity: adaptation of a microtiter plate version.
酵母 DEL 检测法检测辐射诱导的细胞毒性和遗传毒性的保护作用:微量滴定板版本的改编。
Radiat Res. 2010 Dec;174(6):719-26. doi: 10.1667/RR2059.1. Epub 2010 Sep 20.
4
How accurate is in vitro prediction of carcinogenicity?体外预测致癌性的准确性如何?
Br J Pharmacol. 2011 Mar;162(6):1250-8. doi: 10.1111/j.1476-5381.2010.01131.x.
5
Cell cycle dependence of ionizing radiation-induced DNA deletions and antioxidant radioprotection in Saccharomyces cerevisiae.酵母细胞中电离辐射诱导的 DNA 缺失与抗氧化辐射保护的细胞周期依赖性。
Radiat Res. 2010 Jun;173(6):802-8. doi: 10.1667/RR1661.1.