Contrasting incidence of ras mutations in rat mammary and mouse skin tumors induced by anti-benzo[c]phenanthrene-3,4-diol-1,2-epoxide

Zeev A. Ronai, Scott Gradia, Karam El-bayoumy, Shantu Amin, Stephen S. Hecht

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

Racemic anti-benzo[c]phenanthrene-3,4-diol-l,2-epoxide (anti-B[c]PhDE) is a powerful rat mammary carcinogen and is one of the most potent diol-epoxide tumorigens in mouse skin. Activation of ras genes has been proposed to be involved in tumorigenesis by this and related polynuclear aromatic hydrocarbon metabolites. Therefore, we analyzed rat mammary tumors and mouse skin tumors induced by anti-B[c]PhDE for mutations at codons 12, 13 and 61 of the Ki-ras and Ha-ras genes. No Ki-ras mutations were detected in either tumor type. In the rat mammary tumors, no Ha-ras mutations in codons 12 or 13 were observed in 25 tumors analyzed. Only one, a CAA→CTA mutation, was detected in codon 61, of 42 tumors analyzed. These results indicate that Ki-ras and Ha-ras mutations are not involved in the induction of rat mammary tumors by anti-B[c]PhDE. Mutations in codon 61 of the Ha-ras gene were common, however, in mouse skin tumors induced by this diol-epoxide, being detected in 63% of the tumors analyzed; 90% of these mutations were CAA→CTA. A dose-dependent difference in the occurrence of the CAA→CTA mutations was observed; they were present in 75% of the tumors induced by a 100 nmol initiating dose of the diolepoxide, but in only 34.5% of the tumors induced by a 400 nmol initiating dose. A CAA→CTA mutation in codon 61 of Ha-ras was also detected in one of four acetone control tumors. In comparison with previous studies of other polynuclear aromatic hydrocarbons and their metabolites, the results suggest that the reactivity with DNA of anti-B[c]PhDE is one factor involved in the induction of A mutations in Ha-ras genes in mouse skin, but further studies are required to evaluate the significance of these mutations in mouse skin tumorigenesis.

Original languageEnglish (US)
Pages (from-to)2113-2116
Number of pages4
JournalCarcinogenesis
Volume15
Issue number10
DOIs
StatePublished - Oct 1994

All Science Journal Classification (ASJC) codes

  • Cancer Research

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