The in vivo comet assay:: use and status in genotoxicity testing

被引:190
作者
Brendler-Schwaab, S
Hartmann, A
Pfuhler, S
Speit, G [1 ]
机构
[1] Univ Ulm, Abt Humangenet, D-89069 Ulm, Germany
[2] Fed Inst Drugs & Med Devices, Bonn, Germany
[3] Novartis Pharma AG, Basel, Switzerland
[4] Wella AG, Darmstadt, Germany
关键词
D O I
10.1093/mutage/gei033
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The in vivo comet assay (single cell gel electrophoresis assay) in its alkaline version (pH > 13) is being increasingly used in genotoxicity testing of substances such as industrial chemicals, biocides, agrochemicals, food additives and pharmaceuticals. Recommendations for an appropriate performance of the test using OECD guidelines for other in vivo genotoxicity tests have been published. In this review, we critically discuss the biological significance of comet assay effects in general and the status of the test in current strategies for genotoxicity testing. Examples for practical applications of the in vivo comet assay and potential consequences of positive and negative test results are given. The significance of comet assay results for hazard identification and risk assessment is discussed. In accordance with international guidelines for genotoxicity testing the in vivo comet assay is recommended for follow-up testing of positive in vitro findings. It is particularly useful as a tool for the evaluation of local genotoxicity, especially for organs/cell types which cannot easily be evaluated with other standard tests. A positive result in an appropriately performed in vivo comet assay indicates genotoxicity of the test compound in the tissue tested and gains particular significance when a mutagenic potential of the test compound has already been demonstrated in vitro. Such findings will have practical consequences in the risk assessment processes and further development of substances.
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页码:245 / 254
页数:10
相关论文
共 61 条
[51]   In vivo genotoxicity of ortho-phenylphenol, biphenyl, and thiabendazole detected in multiple mouse organs by the alkaline single cell gel electrophoresis assay [J].
Sasaki, YF ;
Saga, A ;
Akasaka, M ;
Yoshida, K ;
Nishidate, E ;
Su, YQ ;
Matsusaka, N ;
Tsuda, S .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1997, 395 (2-3) :189-198
[52]   Detection of in vivo genotoxicity of haloalkanes and haloalkenes carcinogenic to rodents by the alkaline single cell gel electrophoresis (comet) assay in multiple mouse organs [J].
Sasaki, YF ;
Saga, A ;
Akasaka, M ;
Ishibashi, S ;
Yoshida, K ;
Su, YQ ;
Matsusaka, N ;
Tsuda, S .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1998, 419 (1-3) :13-20
[53]   The comet assay with 8 mouse organs: results with 39 currently used food additives [J].
Sasaki, YF ;
Kawaguchi, S ;
Kamaya, A ;
Ohshita, M ;
Kabasawa, K ;
Iwama, K ;
Taniguchi, K ;
Tsuda, S .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2002, 519 (1-2) :103-119
[54]   In vivo studies on genotoxicity of pure and commercial linuron [J].
ScassellatiSforzolini, G ;
Pasquini, R ;
Moretti, M ;
Villarini, M ;
Fatigoni, C ;
Dolara, P ;
Monarca, S ;
Caderni, G ;
Kuchenmeister, F ;
Schmezer, P ;
PoolZobel, BL .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1997, 390 (03) :207-221
[55]   THE CONTRIBUTION OF EXCISION-REPAIR TO THE DNA EFFECTS SEEN IN THE ALKALINE SINGLE-CELL GEL TEST (COMET ASSAY) [J].
SPEIT, G ;
HARTMANN, A .
MUTAGENESIS, 1995, 10 (06) :555-559
[56]   Genotoxicity assessment of the antiepileptic drug AMP397, an Ames-positive aromatic nitro compound [J].
Suter, W ;
Hartmann, A ;
Poetter, F ;
Sagelsdorff, P ;
Hoffmann, P ;
Martus, HJ .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2002, 518 (02) :181-194
[57]  
TGD, 2003, TECHN GUID DOC SUPP
[58]  
Tice RR, 2000, ENVIRON MOL MUTAGEN, V35, P206, DOI 10.1002/(SICI)1098-2280(2000)35:3<206::AID-EM8>3.0.CO
[59]  
2-J
[60]  
*US EPA, 1998, PEST FACT HDB, P489