{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Zeiger E"],"funding":["Health and Environmental Sciences Institute","Intramural NIH HHS","Blanket Purchase Agreement Order","U.S. Food and Drug Administration (FDA); Office of Dietary Supplement Programs and Department of Health and Human Services (HHS); National Institute of Environmental Health Sciences (NIEHS); Division of Translational Toxicology, Office of Liaison, Policy, and Review; and Health and Environmental Sciences Institute (HESI) via Department of the Interior (DOI) Federal Consulting Group (FCG)","Food and Drug Administration (FDA)","Intramural Research Program of the NIH, National Institute of Environmental Health Sciences, Intramural Research project"],"pagination":["116-120"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11241522"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["65(3-4)"],"pubmed_abstract":["The Ames test is required by regulatory agencies worldwide for assessing the mutagenic and carcinogenic potential of chemical compounds. This test uses several strains of bacteria to evaluate mutation induction: positive results in the assay are predictive of rodent carcinogenicity. As an initial step to understanding how well the assay may detect mutagens present as constituents of complex mixtures such as botanical extracts, a cross-sector working group examined the within-laboratory reproducibility of the Ames test using the extensive, publicly available National Toxicology Program (NTP) Ames test database comprising more than 3000 distinct test articles, most of which are individual chemicals. This study focused primarily on NTP tests conducted using the standard Organization for Economic Co-operation and Development Test Guideline 471 preincubation test protocol with 10% rat liver S9 for metabolic activation, although 30% rat S9 and 10 and 30% hamster liver S9 were also evaluated. The reproducibility of initial negative responses in all strains with and without 10% S9, was quite high, ranging from 95% to 99% with few exceptions. The within-laboratory reproducibility of initial positive responses for strains TA98 and TA100 with and without 10% rat liver S9 was ≥90%. Similar results were seen with hamster S9. As expected, the reproducibility of initial equivocal responses was lower, <50%. These results will provide context for determining the optimal design of recommended test protocols for use in screening both individual chemicals and complex mixtures, including botanicals."],"journal":["Environmental and molecular mutagenesis"],"pubmed_title":["Within-laboratory reproducibility of Ames test results: Are repeat tests necessary?"],"pmcid":["PMC11241522"],"funding_grant_id":["ZIA ES103316-04","Z99 ES999999","140D0421F0068","ZIA ES103316"],"pubmed_authors":["Liao Y","Mitchell CA","Zeiger E","Witt KL","Pfuhler S"],"additional_accession":[]},"is_claimable":false,"name":"Within-laboratory reproducibility of Ames test results: Are repeat tests necessary?","description":"The Ames test is required by regulatory agencies worldwide for assessing the mutagenic and carcinogenic potential of chemical compounds. This test uses several strains of bacteria to evaluate mutation induction: positive results in the assay are predictive of rodent carcinogenicity. As an initial step to understanding how well the assay may detect mutagens present as constituents of complex mixtures such as botanical extracts, a cross-sector working group examined the within-laboratory reproducibility of the Ames test using the extensive, publicly available National Toxicology Program (NTP) Ames test database comprising more than 3000 distinct test articles, most of which are individual chemicals. This study focused primarily on NTP tests conducted using the standard Organization for Economic Co-operation and Development Test Guideline 471 preincubation test protocol with 10% rat liver S9 for metabolic activation, although 30% rat S9 and 10 and 30% hamster liver S9 were also evaluated. The reproducibility of initial negative responses in all strains with and without 10% S9, was quite high, ranging from 95% to 99% with few exceptions. The within-laboratory reproducibility of initial positive responses for strains TA98 and TA100 with and without 10% rat liver S9 was ≥90%. Similar results were seen with hamster S9. As expected, the reproducibility of initial equivocal responses was lower, <50%. These results will provide context for determining the optimal design of recommended test protocols for use in screening both individual chemicals and complex mixtures, including botanicals.","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Mar-Apr","modification":"2025-06-28T03:05:40.267Z","creation":"2025-06-28T03:05:40.267Z"},"accession":"S-EPMC11241522","cross_references":{"pubmed":["38651401"],"doi":["10.1002/em.22597"]}}