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High microsome-mediated mutagenicity of the 3,4-dihydrodiol of 7-methylbenz[a]anthracene in S. typhimurium TA 98.
Authors:C Malaveille  B Tierney  P L Grover  P Sims  H Bartsch
Affiliation:1. Unit of Chemical Carcinogenesis, International Agency for Research on Cancer, 150 cours Albert Thomas, 69008 Lyon, France;2. The Chester Beatty Research Institute, Institute of Cancer Research: Royal Cancer Hospital, Fulham Road, London SW3 6JB, England
Abstract:7-Methylbenz[a]anthracene and the 1,2-, 3,4-, 5,6- and 8,9-dihydrodiols derived from this hydrocarbon have been tested for mutagenicity towards S. typhimurium TA 98 in the presence of rat-liver post-mitochondrial supernatant. At non-toxic concentrations, the mutagenicity of the non-K-region 3,4-dihydrodiol was more than ten-fold higher than that of the other K-region and non-K-region dihydrodiols and more than three-fold higher than that of the parent hydrocarbon. 1,1,1-Trichloropropene 2,3-oxide, an inhibitor of epoxide hydratase, increased the microsome-mediated mutagenicity of 7-methylbenz[a]anthracene but did not alter that of the four related dihydrodiols.
Keywords:To whom correspondence and reprint requests should be addressed
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