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Dibenz(a,c)anthracene: a potent inhibitor of skin-tumor initiation by 7,12-dimethylbenz(a)anthracene

Journal Article · · Res. Commun. Chem. Pathol. Pharmacol.; (United States)
OSTI ID:6040807

The mechanism by which the weak tumor initiator dibenz(a,c)anthracene (DB(a,c)A) inhibits the skin-tumor-initiating activity of 7,12-dimethylbenz(a)anthracene (DMBA) was investigated. DB(a,c)A was found to be a potent inhibitor of DMBA initiation when given either 5 min, or 1, 12, or 36 hours before DMBA. Pretreatment of mice with unlabeled DB(a,c)A at either 1, 12, or 36 hours before killing increased the in vitro epidermally mediated covalent binding of (/sup 3/H)DMBA to DNA more than pretreatment with unlabeled DMBA at comparable times. Only when the tumor experiments were mimicked did a decrease in DMBA covalent binding to DNA in vitro occur. The results suggest that some competition at the level of polycyclic hydrocarbon metabolism or at the genome level may exist between metabolites of the weak carcinogen and those of the strong carcinogen.

OSTI ID:
6040807
Journal Information:
Res. Commun. Chem. Pathol. Pharmacol.; (United States), Journal Name: Res. Commun. Chem. Pathol. Pharmacol.; (United States) Vol. 19:3; ISSN RCOCB
Country of Publication:
United States
Language:
English