Carcinogenicity And Mutagenicity Of Benz(A)Anthracene Diols And Diol-Epoxides 1

Thomas J. Slaga, Eliezer Huberman, James K. Selkirk, Ronald G. Harvey, William M. Bracken

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88 Scopus citations

Abstract

Benz(a)anthracene (BA) and its five possible trans-di-hydrodiols were evaluated for determination of their skin tumor-initiating activity and their mutagenic activity in Chinese hamster V79 cells. In addition, the skin tumor-initiating abilities of five diol-epoxides of BA were tested. Results showed (±)-trans-3,4-dihydroxy-3,4-dihydrobenz-(a)anthracene (BA 3,4-dihydrodiol) to be approximately 10 times more mutagenic than was BA and about 20 times more mutagenic than were the other possible dihydrodiols in the V79 cells cocultivated with irradiated hamster embryo cells. As a skin tumor initiator, BA 3,4-dihydrodiol was approximately 5 times more active than BA, whereas the other BA dihydrodiols were all less active tumor initiators. (±trans-3α,4β-Dihydroxy-1α,2α-epoxy-1,2,3,4-tetrahydrobenz(a)anthracene was found to be approximately 20% more active as a tumor initiator than was BA 3,4-dihydrodiol, whereas the other diol-epoxides of BA were less active than BA itself. The results suggest that the bay-region diol-epoxide of BA may be the ultimate carcinogenic and mutagenic form of BA.

Original languageEnglish (US)
Pages (from-to)1699-1704
Number of pages6
JournalCancer Research
Volume38
Issue number6
StatePublished - Jun 1978
Externally publishedYes

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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  • Cite this

    Slaga, T. J., Huberman, E., Selkirk, J. K., Harvey, R. G., & Bracken, W. M. (1978). Carcinogenicity And Mutagenicity Of Benz(A)Anthracene Diols And Diol-Epoxides 1. Cancer Research, 38(6), 1699-1704.