Anticarcinogenic and cocarcinogenic effects of benzo[e]pyrene and dibenz[a,c]anthracene on skin tumor initiation by polycyclic hydrocarbons

Carcinogenesis. 1982;3(4):371-5. doi: 10.1093/carcin/3.4.371.

Abstract

In the present study, we have examined the effects of benzo[e]pyrene (B[e]P) and dibenz[a,c]anthracene (DB[a,c]A) on the skin tumor-initiating activities of methylated and non-methylated polycyclic aromatic hydrocarbons (PAH). B[e]P, when applied 5 min prior to initiation with seven different PAH skin carcinogens, effectively inhibited the tumor-initiating activities of 7,12-dimethylbenz[a]anthracene (DMBA) and dibenz[a,h]anthracene (DB[a,h]A) but had little or no effect on the tumor-initiating activities of 3-methyl-cholanthrene (MCA), 7-methylbenz[a]anthracene (7-MBA), 12-methylbenz[a]anthracene (12-MBA), and 5-methyl-chrysene (5-MeC). B[e]P potentiated the tumor-initiating activity of benzo[a]pyrene (B[a]P) by approximately 30%, DB[a,c]A, when applied 5 min prior to initiation, inhibited the tumor-initiating activities of DMBA, MCA, and DB[a,h]A but had little or no effect on the tumor-initiating activities of B[a]P, 7-MBA, 12-MBA, and 5-MeC. DB[a,c]A, when applied 12, 24, or 36 h prior to initiation with B[a]P, which allowed time for induction of epidermal monooxygenase enzymes, inhibited tumor initiation. The covalent binding of DMBA and B[a]P to epidermal DNA was examined under the influence of B[e]P. Doses of 20 and 200 nmol B[e]P given 5 min prior to 10 nmol [3H]DMBA reduced binding to 47 and 22%, respectively, of the control value. In contrast, doses of 200 or 2000 nmol B[e]P given 5 min prior to 200 nmol [3H]B[a]P had little or no effect on total binding. The data indicate that one cannot predict anti and cocarcinogenic effects of B[e]P and DB[a,c]A on the basis of a presence or absence of a methyl substituent. In addition, fundamental differences exist in the processing and metabolism of DMBA and B[a]P by mouse epidermal cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 9,10-Dimethyl-1,2-benzanthracene / metabolism
  • 9,10-Dimethyl-1,2-benzanthracene / toxicity
  • Animals
  • Benz(a)Anthracenes / pharmacology
  • Benz(a)Anthracenes / toxicity*
  • Benzo(a)pyrene
  • Benzopyrenes / metabolism
  • Benzopyrenes / pharmacology
  • Benzopyrenes / toxicity*
  • DNA / metabolism
  • Drug Interactions
  • Female
  • Methylcholanthrene / toxicity
  • Mice
  • Mice, Inbred Strains
  • Skin Neoplasms / chemically induced*
  • Skin Neoplasms / prevention & control

Substances

  • Benz(a)Anthracenes
  • Benzopyrenes
  • dibenzanthracenes
  • Benzo(a)pyrene
  • Methylcholanthrene
  • 9,10-Dimethyl-1,2-benzanthracene
  • DNA