Revisiting the bacterial mutagenicity assays: Report by a workgroup of the International Workshops on Genotoxicity Testing (IWGT).


Journal

Mutation research. Genetic toxicology and environmental mutagenesis
ISSN: 1879-3592
Titre abrégé: Mutat Res Genet Toxicol Environ Mutagen
Pays: Netherlands
ID NLM: 101632149

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 17 10 2019
accepted: 09 01 2020
entrez: 24 2 2020
pubmed: 24 2 2020
medline: 23 4 2020
Statut: ppublish

Résumé

The International Workshop on Genotoxicity Testing (IWGT) meets every four years to obtain consensus on unresolved issues associated with genotoxicity testing. At the 2017 IWGT meeting in Tokyo, four sub-groups addressed issues associated with the Organization for Economic Cooperation and Development (OECD) Test Guideline TG471, which describes the use of bacterial reverse-mutation tests. The strains sub-group analyzed test data from >10,000 chemicals, tested additional chemicals, and concluded that some strains listed in TG471 are unnecessary because they detected fewer mutagens than other strains that the guideline describes as equivalent. Thus, they concluded that a smaller panel of strains would suffice to detect most mutagens. The laboratory proficiency sub-group recommended (a) establishing strain cell banks, (b) developing bacterial growth protocols that optimize assay sensitivity, and (c) testing "proficiency compounds" to gain assay experience and establish historical positive and control databases. The sub-group on criteria for assay evaluation recommended that laboratories (a) track positive and negative control data; (b) develop acceptability criteria for positive and negative controls; (c) optimize dose-spacing and the number of analyzable doses when there is evidence of toxicity; (d) use a combination of three criteria to evaluate results: a dose-related increase in revertants, a clear increase in revertants in at least one dose relative to the concurrent negative control, and at least one dose that produced an increase in revertants above control limits established by the laboratory from historical negative controls; and (e) establish experimental designs to resolve unclear results. The in silico sub-group summarized in silico utility as a tool in genotoxicity assessment but made no specific recommendations for TG471. Thus, the workgroup identified issues that could be addressed if TG471 is revised. The companion papers (a) provide evidence-based approaches, (b) recommend priorities, and (c) give examples of clearly defined terms to support revision of TG471.

Identifiants

pubmed: 32087853
pii: S1383-5718(20)30007-3
doi: 10.1016/j.mrgentox.2020.503137
pii:
doi:

Substances chimiques

Mutagens 0

Types de publication

Consensus Development Conference Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

503137

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no conflicts of interest.

Auteurs

Rita Schoeny (R)

Rita Schoeny, LLC, Washington, DC 20002, United States. Electronic address: ritas50@verizon.net.

Kevin P Cross (KP)

Leadscope, Inc., 1393 Dublin Road, Columbus, OH 43215, United States.

David M DeMarini (DM)

U.S. Environmental Protection Agency, Research Triangle Park, NC 27711, United States.

Rosalie Elespuru (R)

U.S. Food and Drug Administration, Center for Devices and Radiological Health, Silver Spring, MD 20993, United States.

Atsushi Hakura (A)

Tsukuba Drug Safety, Eisai Co., Ltd., Tsukuba, Ibaraki, 300-2635, Japan.

Dan D Levy (DD)

U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, College Park, MD 20740 United States.

Richard V Williams (RV)

Lhasa Limited, 2 Canal Wharf, Leeds, LS11 5PS, United Kingdom.

Errol Zeiger (E)

Errol Zeiger Consulting, 800 Indian Springs Road, Chapel Hill, NC 27514, United States.

Patricia A Escobar (PA)

Merck & Co., West Point, PA 19486, United States.

Jonathan R Howe (JR)

GSK R&D, Hertfordshire, United Kingdom.

Masayuki Kato (M)

CMIC Pharma Science Co., Ltd., Hokuto, Yamanashi, Japan.

Jasmin Lott (J)

Boehringer Ingelheim Pharma GmbH & Co., KG, Birkendorfer Strasse 65, 88397 Biberach an der Riss, Germany.

Martha M Moore (MM)

Ramboll US Corporation Little Rock, AR 72223, United States.

Stephanie Simon (S)

Merck KGaA, Frankfurter Straβe 250, Darmstadt, 64293, Germany.

Leon F Stankowski (LF)

Charles River Laboratories - Skokie, LLC, 8025 Lamon Ave., Skokie, IL 60077, United States.

Kei-Ichi Sugiyama (KI)

Division of Genetics and Mutagenesis, National Institute of Health Sciences, Kawasaki, Kanagawa, 210-9501, Japan.

Bas-Jan M van der Leede (BM)

Non-Clinical Safety Janssen R&D, a Division of Janssen Pharmaceutica N.V., Beerse, Belgium.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH