Abstract
Aryl hydrocarbon (benzo[a]pyrene) hydroxylase induction in C57BL/6N and DBA/2N inbred mice and their progeny by aromatic hydrocarbons is most likely controlled by a single autosomal dominant trait in skin, peritoneal lining, and lung, as has been previously illustrated for induction of the enzyme in liver, kidney, and bowel; additional factors may influence the expression in skin, peritoneal lining, and lung, however. The susceptibility to tumorigenesis produced by the topical application of benzo[a]pyrene and promotion by phorbol ester or by the intraperitoneal administration of large doses of benzo[a]pyrene is not correlated with the genetically mediated presence or absence of the hydroxylase induction in littermates of back-crosses and intercrosses among the C57BL/6N, DBA/2N, and NZW/BLN strains. Therefore, if this enzyme is necessary for metabolic activation of benzo[a]pyrene to the proximal carcinogen, the basal levels of the hydroxylase are sufficient. Compared with application of 7,12-dimethylbenz[a]anthracene directly to the skin, the intraperitoneal administration of the carcinogen is at least 25 times more effective in causing tumors at the site of promotion. This phenomenon may reflect either circulation of carcinogens metabolically activated by liver enzyme systems or circulation of existing viruses, perhaps subviral particles, activated by the parent polycyclic hydrocarbon molecule or its metabolism.
ACKNOWLEDGMENT We appreciate the help of Dr. Alan S. Rabson (National Cancer Institute) in obtaining the pathological identifications of each tumor produced by the intraperitoneal injection of BP.
- Copyright ©, 1973, by Academic Press, Inc.
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