Literature DB >> 9062586

Evaluation of the rodent micronucleus assay in the screening of IARC carcinogens (groups 1, 2A and 2B) the summary report of the 6th collaborative study by CSGMT/JEMS MMS. Collaborative Study of the Micronucleus Group Test. Mammalian Mutagenicity Study Group.

T Morita1, N Asano, T Awogi, Y F Sasaki, S Sato, H Shimada, S Sutou, T Suzuki, A Wakata, T Sofuni, M Hayashi.   

Abstract

To assess the correlation between micronucleus induction and human carcinogenicity, the rodent micronucleus assay was performed on known and potential human carcinogens in the 6th MMS/CSGMT collaborative study. Approximately 100 commercially available chemicals and chemical groups on which there was little or no micronucleus assay data were selected from IARC (International Agency for Research on Cancer) Groups 1 (human carcinogen), 2A (probable human carcinogen) and 2B (possible human carcinogen). As minimum requirements for the collaborative study, 5 male mice were treated by intraperitoneal injection or oral gavage once or twice with each chemical at three dose levels, and bone marrow and/or peripheral blood was analyzed. Five positives and 2 inconclusives out of 13 Group 1 chemicals, 7 positives and 5 inconclusives of 23 Group 2A chemicals, and 26 positives and 6 inconclusives of 67 Group 2B chemicals were found. Such low positive rates were not surprising because of a test chemical selection bias, and we excluded well-known micronucleus inducers. The overall evaluation of the rodent micronucleus assay was based on the present data combined with published data on the IARC carcinogens. After merging, the positive rates for Groups 1, 2A and 2B were 68.6, 54.5 and 45.6%, respectively. Structure-activity relationship analysis suggested that the micronucleus assay is more sensitive to the genetic toxicity of some classes of chemicals. Those to which it is sensitive consist of (1) aziridines and bis(2-chloroethyl) compounds; (2) alkyl sulfonate and sulfates; (3) acyl-type N-nitroso compounds; (4) hydrazines; (5) aminobiphenyl and benzidine derivatives; and (6) azo compounds. Those to which it is less sensitive consist of (1) dialkyl type N-nitroso compounds; (2) silica and metals and their compounds; (3) aromatic amines without other functional groups; (4) halogenated compounds; and (5) steroids and other hormones. After incorporation of structure-activity relationship information, the positive rates of the rodent micronucleus assay became 90.5, 65.2 and 60.0% for IARC Groups 1, 2A and 2B, respectively. Noteworthy was the tendency of the test to be more sensitive to those carcinogens with stronger evidence human carcinogenicity.

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Year:  1997        PMID: 9062586     DOI: 10.1016/s1383-5718(96)00070-8

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  27 in total

1.  In vitro erythropoiesis from bone marrow-derived progenitors provides a physiological assay for toxic and mutagenic compounds.

Authors:  J Shuga; J Zhang; L D Samson; H F Lodish; L G Griffith
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-14       Impact factor: 11.205

Review 2.  Critical review of styrene genotoxicity focused on the mutagenicity/clastogenicity literature and using current organization of economic cooperation and development guidance.

Authors:  Martha M Moore; Lynn H Pottenger; Tamara House-Knight
Journal:  Environ Mol Mutagen       Date:  2019-03-13       Impact factor: 3.216

3.  Intraperitoneal sodium metavanadate exposure induced severe clinicopathological alterations, hepato-renal toxicity and cytogenotoxicity in African giant rats (Cricetomys gambianus, Waterhouse, 1840).

Authors:  Ifukibot Levi Usende; Chibuisi G Alimba; Benjamin O Emikpe; Adekunle A Bakare; James Olukayode Olopade
Journal:  Environ Sci Pollut Res Int       Date:  2018-07-06       Impact factor: 4.223

4.  Phenotype-based identification of mouse chromosome instability mutants.

Authors:  Naoko Shima; Suzanne A Hartford; Ted Duffy; Lawriston A Wilson; Kerry J Schimenti; John C Schimenti
Journal:  Genetics       Date:  2003-03       Impact factor: 4.562

Review 5.  Estimating the carcinogenic potency of chemicals from the in vivo micronucleus test.

Authors:  Lya G Soeteman-Hernández; George E Johnson; Wout Slob
Journal:  Mutagenesis       Date:  2015-07-10       Impact factor: 3.000

6.  Comet assay evaluation of six chemicals of known genotoxic potential in rats.

Authors:  Cheryl A Hobbs; Leslie Recio; Michael Streicker; Molly H Boyle; Jin Tanaka; Atsushi Shiga; Kristine L Witt
Journal:  Mutat Res Genet Toxicol Environ Mutagen       Date:  2015-03-07       Impact factor: 2.873

7.  Comparison of flow cytometry- and microscopy-based methods for measuring micronucleated reticulocyte frequencies in rodents treated with nongenotoxic and genotoxic chemicals.

Authors:  Kristine L Witt; Elizabeth Livanos; Grace E Kissling; Dorothea K Torous; William Caspary; Raymond R Tice; Leslie Recio
Journal:  Mutat Res       Date:  2007-08-11       Impact factor: 2.433

8.  In vivo micronucleus test in the assessment of cytogenotoxicity of landfill leachates in three animal models from various ecological habitats.

Authors:  Chibuisi G Alimba; Adekunle A Bakare
Journal:  Ecotoxicology       Date:  2015-11-20       Impact factor: 2.823

9.  Protective effect of Withaferin-A on micronucleus frequency and detoxication agents during experimental oral carcinogenesis.

Authors:  Kuppusamy Panjamurthy; Shanmugam Manoharan; Subramanian Balakrishnan; Kathiresan Suresh; Madhavan R Nirmal; Namasivayam Senthil; Linsa Marry Alias
Journal:  Afr J Tradit Complement Altern Med       Date:  2008-10-25

10.  The mouse genomic instability mutation chaos1 is an allele of Polq that exhibits genetic interaction with Atm.

Authors:  Naoko Shima; Robert J Munroe; John C Schimenti
Journal:  Mol Cell Biol       Date:  2004-12       Impact factor: 4.272

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