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The binding of 7,12-dimethylbenz[a]anthracene (DMBA) to DNA was examined in Syrian hamster and Wistar rat embryo cell cultures exposed to DMBA for 5, 24, 48 and 72 h. The level of binding of DMBA to DNA was about twice as great in the hamster embryo cells as in the rat embryo cells at all times. Analysis of the DMBA-deoxyribonucleoside adducts by immobilized boronate chromatography demonstrated that the ratio of adducts with no cis vicinal hydroxyl groups to those containing cis vicinal hydroxyl groups was much greater in the rat embryo cells (from 2.2:1 to 2.9:1) than in the hamster embryo cells (from 1.3:1 to 1.6:1). The hamster embryo cells contained three major DMBADE-DNA adducts: based upon their chromatographic behavior and comparison with the three major DMBA-DNA adducts described by Dipple et al. in mouse embryo cell cultures (Biochemistry, 24 (1985) 2291), two were tentatively identified as resulting from the reaction of anti-DMBADE (the isomer of 1,2-epoxy-3,4-dihydroxy-1,2,3,4-tetrahydro-DMBA with the epoxide and benzylic hydroxyl on the opposite faces of the molecule) with deoxyguanosine and deoxyadenosine and one adduct resulted from reaction of syn-DMBADE (epoxide and benzylic hydroxyl on the same face of the molecule) with deoxyadenosine. The anti-DMBADE-deoxyguanosine, syn-DMBADE-deoxyadenosine, and anti-DMBADE-deoxyadenosine adducts were present in hamster embryo cell DNA in a ratio of 1.2:2:1. The Wistar rat embryo cell DNA contained a much larger proportion of the syn-DMBADE-deoxyadenosine adduct. The relative proportions of the three major DMBA-DNA adducts in Syrian hamster embryo cells were similar at all times, but the proportion of syn-DMBADE-deoxyadenosine adduct decreased slightly with time in the rat embryo cells. These results indicate that there are species specific differences in the stereospecificity of activation of DMBA to DNA-binding diol epoxides which parallel those observed for benzo[a]pyrene (BaP). The high proportion of deoxyadenosine adducts suggests that they may have an important role in the induction of biological effects by DMBA.
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
April 1988,
Cancer research,
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
October 1978,
Cancer research,
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
September 1983,
Cancer letters,
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
April 1977,
Xenobiotica; the fate of foreign compounds in biological systems,
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
May 1988,
Journal of the National Cancer Institute,
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
January 1983,
Cancer research,
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
January 1986,
Carcinogenesis,
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
February 1978,
Chemico-biological interactions,
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
April 1979,
Cancer letters,
S M Sebti, and
T A Smolarek, and
C P Salmon, and
W M Baird
January 1971,
Archiv fur Geschwulstforschung,
