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[Cancer Research 43, 4132-4135, September 1, 1983]
© 1983 American Association for Cancer Research

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Evidence That Binding of 7,12-Dimethylbenz(a)anthracene to DNA in Mouse Embryo Cell Cultures Results in Extensive Substitution of both Adenine and Guanine Residues1

Anthony Dipple2, Margaret Pigott, Robert C. Moschel and Nina Costantino

Basic Research Program-LBI, Chemical Carcinogenesis Program, Frederick Cancer Research Facility, Frederick, Maryland 21701

Primary mouse embryo cell cultures were grown in the presence of [14C]guanine, labeling primarily deoxyguanosine residues in the cellular DNA, or in the presence of [14C]adenine, labeling both deoxyguanosine and deoxyadenosine residues in the cellular DNA. These cultures were subsequently exposed to 7,12-[3H]dimethylbenz(a)anthracene for 24 hr. The DNA was isolated and hydrolyzed to deoxyribonucleosides, and the 7,12-dimethylbenz(a)anthracene:deoxyribonucleoside adducts were separated chromatographically allowing the three major adducts found to be identified as bay-region anti-dihydrodiol-epoxide:deoxyguanosine and :deoxyadenosine adducts and a bayregion syn-dihydrodiol-epoxide:deoxyadenosine adduct. Therefore, in contrast to what is known for benzo(a)pyrene, substantial amounts of deoxyadenosine adducts are formed with the more potent carcinogen, 7,12-dimethylbenz(a)anthracene.

1 Research sponsored by the National Cancer Institute, Department of Health and Human Services, under Contract N01-CO-23909 with Litton Bionetics, Inc. The contents of this publication do not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the United States Government.

2 To whom requests for reprints should be addressed.

Received 1/20/83. Accepted 5/31/83.




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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1983 by the American Association for Cancer Research.