Abstract
The DNA adducts formed from the potent carcinogen dibenzo[a,l]pyrene (DB[a,l]P) in cultures of Sencar mouse embryo cells and a mouse keratinocyte cell line and in Sencar mouse epidermis in vivo were analyzed by 35S−phosphorothioate postlabeling, immobilized boronate chromatography and reverse-phase HPLC. The results demonstrate that the major DNA adducts result from the activation of DB[a,l]P to DB[a,l]P-11,12-diol-13,14-epoxide. Adducts from both the syn− and anti−isomers of this diol epoxide are formed in cells in culture, but in mouse epidermis only anti−isomer adducts are detected.