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Title: Molecular mechanisms of DNA damage initiated by. alpha. ,. beta. -unsaturated carbonyl compounds as criteria for genotoxicity and mutagenicity

Journal Article · · Environmental Health Perspectives; (USA)
DOI:https://doi.org/10.1289/ehp.908899· OSTI ID:5839611

{alpha},{beta}-Unsaturated carbonyl compounds are important not only from a theoretical but also a practical standpoint. These ubiquitous compounds can interact with DNA through various mechanisms. The predominant interaction is the formation of cyclic 1,N{sup 2}-deoxyguanosine adducts; 7,8-cyclic guanine adducts are also found. The authors have synthesized and characterized the stereoisomers of adducts formed by about 20 {alpha},{beta}-unsaturated carbonyl compounds. The different types of adducts and the mutagenic and genotoxic response can be explained by the molecular structures of the agents. Metabolic epoxidation of the double bond and other metabolic activation, e.g., activation of the nitrogroups via nitroreductases, were also found to contribute to genotoxic and mutagenic activities. The results have further elucidated the genotoxic mechanisms of these compounds; however, additional investigations are required for a complete understanding of the genotoxic activity of this class of compounds.

OSTI ID:
5839611
Journal Information:
Environmental Health Perspectives; (USA), Vol. 88; ISSN 0091-6765
Country of Publication:
United States
Language:
English