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.
引用
收藏
页码:245 / 254
页数:10
相关论文
共 61 条
[1]   Induction of aneuploidy in male mouse germ cells detected by the sperm-FISH assay: a review of the present data base [J].
Adler, ID ;
Schmid, TE ;
Baumgartner, A .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2002, 504 (1-2) :173-182
[2]  
[Anonymous], 1999, IARC Monogr Eval Carcinog Risks Hum, V73, P517
[3]   THE TOXICOLOGICAL EFFECTS OF SACCHARIN IN SHORT-TERM GENOTOXICITY ASSAYS [J].
ARNOLD, DL ;
BOYES, BG .
MUTATION RESEARCH, 1989, 221 (02) :69-132
[4]  
*BFR, 2002, STRAT GEN TEST SUBST
[5]   O-phenylphenol and its sodium and potassium salts:: A toxicological assessment [J].
Bomhard, EM ;
Brendler-Schwaab, SY ;
Freyberger, A ;
Herbold, BA ;
Leser, KH ;
Richter, M .
CRITICAL REVIEWS IN TOXICOLOGY, 2002, 32 (06) :551-625
[6]   CHRONIC TOXICITY CARCINOGENICITY STUDIES OF FD-AND-C YELLOW NO-5 (TARTRAZINE) IN RATS [J].
BORZELLECA, JF ;
HALLAGAN, JB .
FOOD AND CHEMICAL TOXICOLOGY, 1988, 26 (03) :179-187
[7]   A CHRONIC TOXICITY CARCINOGENICITY STUDY OF FD-AND-C YELLOW NO-5 (TARTRAZINE) IN MICE [J].
BORZELLECA, JF ;
HALLAGAN, JB .
FOOD AND CHEMICAL TOXICOLOGY, 1988, 26 (03) :189-194
[8]   LIVER-TUMOR INDUCTION IN B6C3F1 MICE BY DICHLOROACETATE AND TRICHLOROACETATE [J].
BULL, RJ ;
SANCHEZ, IM ;
NELSON, MA ;
LARSON, JL ;
LANSING, AJ .
TOXICOLOGY, 1990, 63 (03) :341-359
[9]   MUTAGENIC ACTIVITY OF 27 DYES AND RELATED CHEMICALS IN THE SALMONELLA MICROSOME AND MOUSE LYMPHOMA TK+/- ASSAYS [J].
CAMERON, TP ;
HUGHES, TJ ;
KIRBY, PE ;
FUNG, VA ;
DUNKEL, VC .
MUTATION RESEARCH, 1987, 189 (03) :223-261
[10]  
Clay P., 1999, Environmental and Molecular Mutagenesis, V33, P20