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. 1981;99(1-2):87-102.
doi: 10.1007/BF00412446.

Test systems for mutagenicity screening of environmental chemicals and their relevance for the evaluation of genetic hazards to man

Test systems for mutagenicity screening of environmental chemicals and their relevance for the evaluation of genetic hazards to man

K Sankaranarayanan. J Cancer Res Clin Oncol. 1981.

Abstract

Mutagenicity test systems play a dual role in public health: (1) to identify chemicals in our environment that are capable of causing genetic alterations and thus pose a threat of genetic damage to generations yet unborn and (2) as a faster screen (than many of the conventional carcinogenicity tests) to identify chemicals with carcinogenic potentials. In this paper the different mutagenicity test systems currently available are reviewed together with a discussion of their advantages and disadvantages. It is argued that our current data base does not permit a realistic quantitative assessment of genetic hazards ensuing from exposure to environmental chemicals and that only qualitative conclusions are possible. A framework which may be useful in the context of the latter is briefly outlined.

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References

    1. Arlett CF (1977) Mutagenicity testing with V 79 Chinese hamster cells. In: Kilbey BJ, Legator M, Nichols W, Ramel C (eds) Handbook of mutagenicity test procedure Elsevier, Amsterdam, pp 175–192
    1. Ashby J, Styles JA (1978) Does carcinogenic potency correlate with mutagenic potency in the Ames assay? Nature 271:452–455 - PubMed
    1. Auerbach C, Robson JM (1946) Chemical production of mutations. Nature 157:302 - PubMed
    1. Baars AJ, Zijlstra JA, Vogel E, Breimer DD (1977) The occurrence of cytochrome P-450 and aryl hydrocarbon hydroxylase activity in Drosophila melanogaster microsomes, and the importance of this metabolizing capacity for the screening of carcinogenic and mutagenic properties of foreign compounds. Mutat Res 44:257–268 - PubMed
    1. Baars AJ, Jansen M, Breimer DD (1979) Xenobiotic-metabolizing enzymes in Drosophila melanogaster: epoxide hydratase and glutathione S transferase activities, compared with similar activities in rat liver. Mutat Res 62:279–291 - PubMed

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