Literature DB >> 26212309

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

Cheryl A Hobbs1, Leslie Recio2, Michael Streicker3, Molly H Boyle4, Jin Tanaka5, Atsushi Shiga6, Kristine L Witt7.   

Abstract

As a part of an international validation of the in vivo rat alkaline comet assay (comet assay) initiated by the Japanese Center for the Validation of Alternative Methods (JaCVAM) we examined six chemicals for potential to induce DNA damage: 2-acetylaminofluorene (2-AAF), N-nitrosodimethylamine (DMN), o-anisidine, 1,2-dimethylhydrazine dihydrochloride (1,2-DMH), sodium chloride, and sodium arsenite. DNA damage was evaluated in the liver and stomach of 7- to 9-week-old male Sprague Dawley rats. Of the five genotoxic carcinogens tested in our laboratory, DMN and 1,2-DMH were positive in the liver and negative in the stomach, 2-AAF and o-anisidine produced an equivocal result in liver and negative results in stomach, and sodium arsenite was negative in both liver and stomach. 1,2-DMH and DMN induced dose-related increases in hedgehogs in the same tissue (liver) that exhibited increased DNA migration. However, no cytotoxicity was indicated by the neutral diffusion assay (assessment of highly fragmented DNA) or histopathology in response to treatment with any of the tested chemicals. Therefore, the increased DNA damage resulting from exposure to DMN and 1,2-DMH was considered to represent a genotoxic response. Sodium chloride, a non-genotoxic non-carcinogen, was negative in both tissues as would be predicted. Although only two (1,2-DMH and DMN) out of five genotoxic carcinogens produced clearly positive results in the comet assay, the results obtained for o-anisidine and sodium arsenite in liver and stomach cells are consistent with the known mode of genotoxicity and tissue specificity exhibited by these carcinogens. In contrast, given the known genotoxic mode-of-action and target organ carcinogenicity of 2-AAF, it is unclear why this chemical failed to convincingly increase DNA migration in the liver. Thus, the results of the comet assay validation studies conducted in our laboratory were considered appropriate for five out of the six test chemicals.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  1,2-Dimethylhydrazine dihydrochloride; 2-Acetylaminofluorene; In vivo comet assay; N-Nitrosodimethylamine; Sodium arsenite; o-Anisidine

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Year:  2015        PMID: 26212309      PMCID: PMC4516904          DOI: 10.1016/j.mrgentox.2015.03.003

Source DB:  PubMed          Journal:  Mutat Res Genet Toxicol Environ Mutagen        ISSN: 1383-5718            Impact factor:   2.873


  41 in total

1.  Recommendations for conducting the in vivo alkaline Comet assay. 4th International Comet Assay Workshop.

Authors:  A Hartmann; E Agurell; C Beevers; S Brendler-Schwaab; B Burlinson; P Clay; A Collins; A Smith; G Speit; V Thybaud; R R Tice
Journal:  Mutagenesis       Date:  2003-01       Impact factor: 3.000

2.  Comparative investigation of multiple organs of mice and rats in the comet assay.

Authors:  Kaoru Sekihashi; Ayumu Yamamoto; Yukie Matsumura; Shunji Ueno; Mie Watanabe-Akanuma; Fekadu Kassie; Siegfried Knasmüller; Shuji Tsuda; Yu F Sasaki
Journal:  Mutat Res       Date:  2002-05-27       Impact factor: 2.433

3.  Collaborative study on fifteen compounds in the rat-liver Comet assay integrated into 2- and 4-week repeat-dose studies.

Authors:  Andreas Rothfuss; Mike O'Donovan; Marlies De Boeck; Dominique Brault; Andreas Czich; Laura Custer; Shuichi Hamada; Ulla Plappert-Helbig; Makoto Hayashi; Jonathan Howe; Andrew R Kraynak; Bas-jan van der Leede; Madoka Nakajima; Catherine Priestley; Veronique Thybaud; Kazuhiko Saigo; Satin Sawant; Jing Shi; Richard Storer; Melanie Struwe; Esther Vock; Sheila Galloway
Journal:  Mutat Res       Date:  2010-07-23       Impact factor: 2.433

4.  Identification of a genotoxic mechanism for the carcinogenicity of the environmental pollutant and suspected human carcinogen o-anisidine.

Authors:  Marie Stiborová; Markéta Miksanová; Miroslav Sulc; Helena Rýdlová; Heinz H Schmeiser; Eva Frei
Journal:  Int J Cancer       Date:  2005-09-20       Impact factor: 7.396

5.  Transplacental carcinogenicity of inorganic arsenic in the drinking water: induction of hepatic, ovarian, pulmonary, and adrenal tumors in mice.

Authors:  Michael P Waalkes; Jerrold M Ward; Jie Liu; Bhalchandra A Diwan
Journal:  Toxicol Appl Pharmacol       Date:  2003-01-01       Impact factor: 4.219

Review 6.  The genotoxicity of sodium saccharin and sodium chloride in relation to their cancer-promoting properties.

Authors:  J Ashby
Journal:  Food Chem Toxicol       Date:  1985 Apr-May       Impact factor: 6.023

7.  Animal models for arsenic carcinogenesis: inorganic arsenic is a transplacental carcinogen in mice.

Authors:  Michael P Waalkes; Jie Liu; Jerrold M Ward; Bhalchandra A Diwan
Journal:  Toxicol Appl Pharmacol       Date:  2004-08-01       Impact factor: 4.219

8.  Detection of genotoxic carcinogens in the in vivo-in vitro hepatocyte DNA repair assay.

Authors:  J C Mirsalis; C K Tyson; B E Butterworth
Journal:  Environ Mutagen       Date:  1982

Review 9.  Arsenic-induced genotoxicity and genetic susceptibility to arsenic-related pathologies.

Authors:  Francesca Faita; Liliana Cori; Fabrizio Bianchi; Maria Grazia Andreassi
Journal:  Int J Environ Res Public Health       Date:  2013-04-12       Impact factor: 3.390

10.  Arsenite as the probable active species in the human carcinogenicity of arsenic: mouse micronucleus assays on Na and K arsenite, orpiment, and Fowler's solution.

Authors:  H Tinwell; S C Stephens; J Ashby
Journal:  Environ Health Perspect       Date:  1991-11       Impact factor: 9.031

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Authors:  Gaochao Han; Zhuangsheng Tan; Haiming Jing; Junyu Ning; Zinan Li; Shan Gao; Guojun Li
Journal:  Biol Trace Elem Res       Date:  2021-01-05       Impact factor: 3.738

2.  Genoprotective effects of gallic acid against cisplatin induced genotoxicity in bone marrow cells of mice.

Authors:  S Shruthi; K Bhasker Shenoy
Journal:  Toxicol Res (Camb)       Date:  2018-06-15       Impact factor: 3.524

3.  Next generation high throughput DNA damage detection platform for genotoxic compound screening.

Authors:  Peter Sykora; Kristine L Witt; Pooja Revanna; Stephanie L Smith-Roe; Jonathan Dismukes; Donald G Lloyd; Bevin P Engelward; Robert W Sobol
Journal:  Sci Rep       Date:  2018-02-09       Impact factor: 4.379

4.  Oxidative damage and DNA repair in desiccated recalcitrant embryonic axes of Acer pseudoplatanus L.

Authors:  Beata P Plitta-Michalak; Alice A Ramos; Piotr Pupel; Marcin Michalak
Journal:  BMC Plant Biol       Date:  2022-01-19       Impact factor: 4.215

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