Reducing risk of false positives in the in vivo comet assay and improving result reliability

IF 2.3 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation research. Genetic toxicology and environmental mutagenesis Pub Date : 2024-03-15 DOI:10.1016/j.mrgentox.2024.503750
Marie Z. Vasquez, Nicole E. Dewhurst
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引用次数: 0

Abstract

The risk of generating false positive in vivo comet assay results can be increased when procedural bias and/or technical variability is poorly controlled. This has been an ongoing concern since comet was first introduced into regulatory safety testing. But the proprietary nature of regulated studies and the 3Rs have limited the ability to conduct and publish the comparative in vivo studies necessary to determine the effect these factors can have on comet assay results when substances other than well characterized positive control compounds are evaluated in multiple tissues. That changed when Helix3 was asked to repeat for regulatory submission three independent in vivo comet studies with positive results generated by three other laboratories evaluating the effects of three different test substances on the liver, duodenum, and stomach. We repeated each study using the same test substance and experimental design as the original labs but with our standard quality control methods implemented to reduce procedural bias and variability. In every case, we generated negative results that regulatory authorities accepted over the initial positive results due to evidence of high technical variability and procedural bias in the original labs and studies. Meanwhile, the International Workshop on Genotoxicity (IWGT) compared >14 years of Helix3 comet historical control data (HCD) to HCD from 6 other experienced comet laboratories and concluded that our data exhibited the highest overall background % tail DNA levels with the lowest inter-study variability resulting in the highest quality HCD of all the labs evaluated. These case studies and the IWGT report suggest that our enhanced quality control methods and higher (>2 % mean of slide median tail DNA) background levels can effectively mitigate the nuisance factors that can generate false positive in vivo comet assay results. To facilitate a better understanding of the technical parameters that can significantly influence the comet results, we describe our enhanced procedures with justifications and examples.

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降低体内彗星试验的假阳性风险,提高结果的可靠性
如果程序偏差和/或技术变异性控制不佳,体内彗星试验结果呈假阳性的风险就会增加。自从彗星首次被引入监管安全测试以来,这一直是一个令人担忧的问题。但由于监管研究的专有性和 3Rs 限制了开展和发布必要的体内比较研究的能力,而这些研究是为了确定在多个组织中评估特征明确的阳性对照化合物以外的物质时,这些因素对彗星测定结果的影响。当Helix3被要求重复其他三家实验室进行的三项独立体内彗星试验,评估三种不同试验物质对肝脏、十二指肠和胃的影响,并得出阳性结果时,情况发生了变化。我们重复了每项研究,使用了与原实验室相同的测试物质和实验设计,但采用了我们的标准质量控制方法,以减少程序偏差和变异性。由于有证据表明原始实验室和研究中存在较高的技术变异性和程序偏差,因此在每项研究中,我们都得出了监管机构接受的阴性结果,而不是最初的阳性结果。与此同时,国际遗传毒性研讨会(IWGT)将 Helix3 14 年的彗星历史控制数据(HCD)与其他 6 家经验丰富的彗星实验室的 HCD 进行了比较,得出的结论是,我们的数据显示出最高的总体背景尾 DNA 百分比水平,研究间的变异性最低,因此在所有接受评估的实验室中,我们的 HCD 质量最高。这些案例研究和 IWGT 报告表明,我们强化的质量控制方法和较高的(玻片中位数尾 DNA 平均值的 2%)背景水平可以有效减少可能导致体内彗星检测结果假阳性的干扰因素。为了便于更好地理解对彗星检测结果有重大影响的技术参数,我们介绍了我们的强化程序,并提供了理由和示例。
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来源期刊
CiteScore
3.80
自引率
5.30%
发文量
84
审稿时长
105 days
期刊介绍: Mutation Research - Genetic Toxicology and Environmental Mutagenesis (MRGTEM) publishes papers advancing knowledge in the field of genetic toxicology. Papers are welcomed in the following areas: New developments in genotoxicity testing of chemical agents (e.g. improvements in methodology of assay systems and interpretation of results). Alternatives to and refinement of the use of animals in genotoxicity testing. Nano-genotoxicology, the study of genotoxicity hazards and risks related to novel man-made nanomaterials. Studies of epigenetic changes in relation to genotoxic effects. The use of structure-activity relationships in predicting genotoxic effects. The isolation and chemical characterization of novel environmental mutagens. The measurement of genotoxic effects in human populations, when accompanied by quantitative measurements of environmental or occupational exposures. The application of novel technologies for assessing the hazard and risks associated with genotoxic substances (e.g. OMICS or other high-throughput approaches to genotoxicity testing). MRGTEM is now accepting submissions for a new section of the journal: Current Topics in Genotoxicity Testing, that will be dedicated to the discussion of current issues relating to design, interpretation and strategic use of genotoxicity tests. This section is envisaged to include discussions relating to the development of new international testing guidelines, but also to wider topics in the field. The evaluation of contrasting or opposing viewpoints is welcomed as long as the presentation is in accordance with the journal''s aims, scope, and policies.
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