Literature DB >> 17113817

Report of the IWGT working group on strategy/interpretation for regulatory in vivo tests II. Identification of in vivo-only positive compounds in the bone marrow micronucleus test.

D J Tweats1, D Blakey, R H Heflich, A Jacobs, S D Jacobsen, T Morita, T Nohmi, M R O'Donovan, Y F Sasaki, T Sofuni, R Tice.   

Abstract

A survey conducted as part of an International Workshop on Genotoxicity Testing (IWGT) has identified a number of compounds that appear to be more readily detected in vivo than in vitro. The reasons for this property varies from compound to compound and includes metabolic differences; the influence of gut flora; higher exposures in vivo compared to in vitro; effects on pharmacology, in particular folate depletion or receptor kinase inhibition. It is possible that at least some of these compounds are detectable in vitro if a specific in vitro test is chosen as part of the test battery, but the 'correct' choice of test may not always be obvious when testing a compound of unknown genotoxicity. It is noted that many of the compounds identified in this study interfere with cell cycle kinetics and this can result in either aneugenicity or chromosome breakage. A decision tree is outlined as a guide for the evaluation of compounds that appear to be genotoxic agents in vivo but not in vitro. The regulatory implications of these findings are discussed.

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Year:  2006        PMID: 17113817      PMCID: PMC2790421          DOI: 10.1016/j.mrgentox.2006.10.006

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


  37 in total

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Authors:  R E Sotomayor; T F Collins
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Journal:  Carcinogenesis       Date:  1996-08       Impact factor: 4.944

4.  MEK, ERK, and p90RSK are present on mitotic tubulin in Swiss 3T3 cells: a role for the MAP kinase pathway in regulating mitotic exit.

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Journal:  Cell Signal       Date:  2001-09       Impact factor: 4.315

5.  Folate and homocysteine status and haemolysis in patients treated with sulphasalazine for arthritis.

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6.  NTP Toxicology and Carcinogenesis Studies of Salicylazosulfapyridine (CAS No. 599-79-1) in F344/N Rats and B6C3F1 Mice (Gavage Studies).

Authors: 
Journal:  Natl Toxicol Program Tech Rep Ser       Date:  1997-05

7.  Evaluation of mutant frequencies of chemically induced tumors and normal tissues in lambda/cII transgenic mice.

Authors:  Jon C Mirsalis; Julie A Shimon; Alphonso Johnson; David Fairchild; Nathan Kanazawa; Tung Nguyen; Johan de Boer; Barry Glickman; Richard A Winegar
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8.  Mechanistic studies on genotoxicity and carcinogenicity of salicylazosulfapyridine an anti-inflammatory medicine.

Authors:  M J Iatropoulos; G M Williams; K M Abdo; F W Kari; R W Hart
Journal:  Exp Toxicol Pathol       Date:  1997-02

9.  Induction of chromosomal damage in mammalian cells in vitro and in vivo by sulfapyridine or 5-aminosalicylic acid.

Authors:  K L Witt; J B Bishop; A F McFee; V Kumaroo
Journal:  Mutat Res       Date:  1992-09       Impact factor: 2.433

Review 10.  Genotoxicity of benzene and its metabolites.

Authors:  John Whysner; M Vijayaraj Reddy; Peter M Ross; Melissa Mohan; Elizabeth A Lax
Journal:  Mutat Res       Date:  2004-03       Impact factor: 2.433

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Journal:  Clin Pharmacol Ther       Date:  2011-05-25       Impact factor: 6.875

4.  Genotoxicity of pemetrexed in human peripheral blood lymphocytes.

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Journal:  Cytotechnology       Date:  2012-11-24       Impact factor: 2.058

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Journal:  Physiol Res       Date:  2020-12-31       Impact factor: 1.881

Review 6.  Genotoxicity of Anesthetics Evaluated In Vivo (Animals).

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Review 7.  A Review on Mutagenicity Testing for Hazard Classification of Chemicals at Work: Focusing on in vivo Micronucleus Test for Allyl Chloride.

Authors:  Kyung-Taek Rim; Soo-Jin Kim
Journal:  Saf Health Work       Date:  2015-06-19

8.  A novel in vitro 3D model of the human bone marrow to bridge the gap between in vitro and in vivo genotoxicity testing.

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Journal:  Mutagenesis       Date:  2022-05-04       Impact factor: 2.954

9.  The benzene metabolite para-benzoquinone is genotoxic in human, phorbol-12-acetate-13-myristate induced, peripheral blood mononuclear cells at low concentrations.

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10.  Evaluation of the Genotoxic Potential of the Selective COX-2 Inhibitor Enflicoxib in a Battery of in vitro and in vivo Genotoxicity Assays.

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