Fourth International Workgroup on Genotoxicity Testing: Results of the in vivo Comet assay workgroup

被引:373
作者
Burlinson, Brian
Tice, Raymond R.
Speit, Gunter
Agurell, Eva
Brendler-Schwaab, Susanne Y.
Collins, Andrew R.
Escobar, Patricia
Honma, Masamitsu
Kumaravel, Tirukalikundram S.
Nakajima, Madoka
Sasaki, Yu F.
Thybaud, Veronique
Uno, Yoshifumi
Vasquez, Marie
Hartmann, Andreas
机构
[1] Huntingdon Life Sci, Cellular & Mol Toxicol, Huntington PE28 4HS, Cambs, England
[2] Natl Inst Environm Hlth Sci, Res Triangle Pk, NC 27709 USA
[3] Univ Ulm Klinikum, Abt Humangenet, D-7900 Ulm, Germany
[4] Med Prod Agcy, Uppsala, Sweden
[5] Fed Inst Drugs & Med Devices, Bonn, Germany
[6] Univ Oslo, Dept Nutr, Oslo, Norway
[7] BioReliance, Invitrogen Bioserv, Rockville, MD USA
[8] Natl Inst Hlth Sci, Tokyo 158, Japan
[9] Bio Safety Res Ctr, Shizuoka, Japan
[10] Hachinohe Natl Coll Technol, Hachinohe, Japan
[11] Sanofi Aventis, Vitry Sur Seine, France
[12] Mitsubishi Chem Safety Inst Ltd, Minato Ku, Tokyo, Japan
[13] Novartis Pharma AG, Safety Profiling & Assessment, Basel, Switzerland
关键词
single cell gel assay; Comet assay; DNA damage; genotoxicity; alkaline electrophoresis;
D O I
10.1016/j.mrgentox.2006.08.011
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
As part of the Fourth International Workshop on Genotoxicity Testing (IWGT), held 9-10 September 2005 in San Francisco, California, an expert working group on the Comet assay was convened to review and discuss some of the procedures and methods recommended in previous documents. Particular attention was directed at the in vivo rodent, alkaline (pH > 13) version of the assay. The aim was to review those protocol areas which were unclear or which required more detail in order to produce a standardized protocol with maximum acceptability by international regulatory agencies. The areas covered were: number of dose levels required, cell isolation techniques, measures of cytotoxicity, scoring of comets (i.e., manually or by image analysis), and the need for historical negative/positive control data. It was decided that a single limit dose was not sufficient although the required number of dose levels was not stipulated. The method of isolating cells was thought not to have a qualitative effect on the assay but more data were needed before a conclusion could be drawn. Concurrent measures of cytotoxicity were required with histopathological examination of tissues for necrosis or apoptosis as the "Gold Standard". As for analysing the comets, the consensus was that image analysis was preferred but not required. Finally, the minimal number of studies required to generate a historical positive or negative control database was not defined; rather the emphasis was placed on demonstrating the stability of the negative/positive control data. It was also agreed that a minimum reporting standard would be developed which would be consistent with OECD in vivo genotoxicity test method guidelines. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:31 / 35
页数:5
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