{"title":"Does the 2-test in vitro genotoxicity battery of Ames plus in vitro micronucleus tests detect relevant substances that induce gene mutations in vivo?","authors":"David Kirkland, Damian Bowen, Paul Fowler","doi":"10.1016/j.mrgentox.2026.503949","DOIUrl":null,"url":null,"abstract":"<div><div>The <em>in vitro</em> genotoxicity testing battery comprising a bacterial gene mutation test (Ames test) and an <em>in vitro</em> micronucleus (MNvit) test is widely recommended by regulatory authorities since it detects the 3 key modes of genotoxic action (gene mutations, clastogenicity and aneuploidy). The recommendations that this battery is acceptable for regulatory use are based on its ability to effectively detect <em>in vivo</em> genotoxins and carcinogens. However, substances inducing gene mutations are a particular concern (representing stable genetic change and a key step in the carcinogenic process), and more <em>in vivo</em> gene mutation data have been published in recent years due to the wider use of transgenic rodent gene mutation (TGR) and <em>Pig-a</em> assays. It is appropriate to question whether the Ames + MNvit battery is efficient at detecting substances that induce gene mutations <em>in vivo</em>. A review of several compilations of genotoxicity studies revealed 26 substances that were reported positive in TGR and/or <em>Pig-a</em> but negative in the Ames test. A detailed analysis showed that 25 of these results were questionable for various reasons, and not robust examples of the failure of the 2-test <em>in vitro</em> battery. Only procarbazine was convincingly positive <em>in vivo</em> but predominantly negative <em>in vitro</em>, and this is mainly due to its complex metabolism which is probably not optimal with standard <em>in vitro</em> metabolic activation systems. The analysis shows no evidence that adding a mammalian cell gene mutation test to the <em>in vitro</em> battery would improve the detection of <em>in vivo</em> gene mutagens.</div></div>","PeriodicalId":18799,"journal":{"name":"Mutation research. Genetic toxicology and environmental mutagenesis","volume":"913 ","pages":"Article 503949"},"PeriodicalIF":2.8000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mutation research. Genetic toxicology and environmental mutagenesis","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1383571826000331","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/13 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The in vitro genotoxicity testing battery comprising a bacterial gene mutation test (Ames test) and an in vitro micronucleus (MNvit) test is widely recommended by regulatory authorities since it detects the 3 key modes of genotoxic action (gene mutations, clastogenicity and aneuploidy). The recommendations that this battery is acceptable for regulatory use are based on its ability to effectively detect in vivo genotoxins and carcinogens. However, substances inducing gene mutations are a particular concern (representing stable genetic change and a key step in the carcinogenic process), and more in vivo gene mutation data have been published in recent years due to the wider use of transgenic rodent gene mutation (TGR) and Pig-a assays. It is appropriate to question whether the Ames + MNvit battery is efficient at detecting substances that induce gene mutations in vivo. A review of several compilations of genotoxicity studies revealed 26 substances that were reported positive in TGR and/or Pig-a but negative in the Ames test. A detailed analysis showed that 25 of these results were questionable for various reasons, and not robust examples of the failure of the 2-test in vitro battery. Only procarbazine was convincingly positive in vivo but predominantly negative in vitro, and this is mainly due to its complex metabolism which is probably not optimal with standard in vitro metabolic activation systems. The analysis shows no evidence that adding a mammalian cell gene mutation test to the in vitro battery would improve the detection of in vivo gene mutagens.
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.