Recommended protocols based on a survey of current practice in genotoxicity testing laboratories: study design.

The most commonly used genotoxicity assays for cultured mammalian cells are mammalian cell mutagenesis, chromosome aberrations/SCE, hepatocyte UDS, and cell transformation. Since their inception, protocols for these assays have been modified in various laboratories. It has been observed that minor but potentially significant method modifications frequently remain unpublished (Swierenga et al., 1983) but should be considered in the development of recommended protocols. The present study was undertaken to determine the current 'state of the art' for these tests. Detailed questionnaires on culture conditions and testing protocols for both stock and test cell populations were designed with the assistance of an international advisory committee and sent to all research and contract laboratories that could be readily identified in Canada, U.S.A. and Europe. Responses from 425 completed questionnaires were analyzed to determine the most commonly used approach and modifications for each procedural step. As expected, the results show a large degree of interlaboratory variation. Detailed protocols for conducting each assay have been prepared and include: stepwise instructions, precautionary measures and practical solutions to common problems associated with each assay; recipes for media and solutions; formulas for quantifying genotoxic responses; reference lists of related assays; guidelines for interpretation; and discussions of the applications, advantages and disadvantages of each test.

[1]  D. Brusick Role of metabolism in short‐term test development , 1989, Environmental and molecular mutagenesis.

[2]  E. Nestmann Mutagen is a mutagen, not necessarily a carcinogen. , 1986, Basic life sciences.

[3]  V. Dunkel,et al.  Recommended protocols based on a survey of current practice in genotoxicity testing laboratories: III. Cell transformation in C3H/10T1/2 mouse embryo cell, BALB/c 3T3 mouse fibroblast and Syrian hamster embryo cell cultures. , 1991, Mutation research.

[4]  C. Rudd,et al.  Recommended protocols based on a survey of current practice in genotoxicity testing laboratories: II. Mutation in Chinese hamster ovary, V79 Chinese hamster lung and L5178Y mouse lymphoma cells. , 1991, Mutation research.

[5]  D. Krewski,et al.  Mutagenicity screening of foods I. Results with beverages. , 1982, Environmental mutagenesis.

[7]  E. Nestmann,et al.  Recommended protocols based on a survey of current practice in genotoxicity testing laboratories: I. Unscheduled DNA synthesis assay in rat hepatocyte cultures. , 1991, Mutation research.

[8]  W. W. Nichols,et al.  Short-term tests for carcinogens and mutagens. , 1979, Mutation research.

[9]  V. Dunkel,et al.  Reliability of the hepatocyte primary culture/DNA repair test in testing of coded carcinogens and noncarcinogens. , 1982, Mutation research.

[10]  R. Tennant,et al.  Chemical structure, Salmonella mutagenicity and extent of carcinogenicity as indicators of genotoxic carcinogenesis among 222 chemicals tested in rodents by the U.S. NCI/NTP. , 1988, Mutation research.

[11]  Joanne T. Emerman,et al.  In vitro toxicity screening tests: A comparison of activation systems and treatment protocols among different laboratories , 1983 .

[12]  J. Heddle,et al.  Recommended protocols based on a survey of current practice in genotoxicity testing laboratories, IV. Chromosome aberration and sister-chromatid exchange in Chinese hamster ovary, V79 Chinese hamster lung and human lymphocyte cultures. , 1991, Mutation research.

[13]  B H Margolin,et al.  Prediction of chemical carcinogenicity in rodents from in vitro genetic toxicity assays. , 1987, Science.

[14]  B. Ames,et al.  Carcinogens are mutagens: a simple test system combining liver homogenates for activation and bacteria for detection. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[15]  M. F. Laspia,et al.  The use of adult rat liver cultures in the detection of the genotoxicity of various polycyclic aromatic hydrocarbons. , 1981, Environmental mutagenesis.