Dibenz[a,c]anthracene: a potent inhibitor of skin-tumor initiation by 7,12-dimethylbenz[a]anthracene.

Abstract

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 [3H]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 suggests 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.

• Authors: T J Slaga, A Viaje, S G Buty, W M Bracken
• Journal: Research communications in chemical pathology and pharmacology (Res Commun Chem Pathol Pharmacol) Vol. 19 Issue 3 Pg. 477-83 (Mar 1978) ISSN: 0034-5164 [Print] United States
• PMID: 418469 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Benz(a)Anthracenes
• 9,10-Dimethyl-1,2-benzanthracene
• DNA

Topics

• 9,10-Dimethyl-1,2-benzanthracene (antagonists & inhibitors, metabolism, pharmacology)
• Animals
• Benz(a)Anthracenes (antagonists & inhibitors, pharmacology)
• DNA (metabolism)
• Female
• In Vitro Techniques
• Mice
• Skin Neoplasms (chemically induced, prevention & control)
• Time Factors