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[Cancer Research 42, 1646-1649, May 1, 1982]
© 1982 American Association for Cancer Research

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Cell-mediated Mutagenicity in Chinese Hamster V79 Cells of Dibenzopyrenes and Their Bay-Region Fluorine-substituted Derivatives1

Bruce S. Hass2, Catherine K. McKeown, Dennis J. Sardella, Eliahu Boger, Pallab K. Ghoshal and Eliezer Huberman3

Biology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830 [B. S. H., C. K. M., E. H.], and Department of Chemistry, Boston College, Chestnut Hill, Massachusetts 02167 [D. J. S., E. B., P. K. G.]

The polycyclic aromatic hydrocarbons dibenzo(a,i)pyrene and dibenzo(a,h)pyrene, each of which possesses two bay regions, and their bay-region difluorinated derivatives were tested for mutagenicity for ouabain and 6-thioguanine resistance in Chinese hamster V79 cells. Since V79 cells do not metabolize polycyclic aromatic hydrocarbons, mutagenesis was tested in both the presence and the absence of golden hamster embryo cells capable of metabolizing polycyclic aromatic hydrocarbons. Neither of the dibenzopyrenes nor their fluorinated derivatives were mutagenic in the absence of the golden hamster embryo cells. In the presence of these cells (cell-mediated assay), both dibenzopyrenes were mutagenic, whereas the difluorinated derivatives, 2,10-difluorodibenzo-(a,i)pyrene and 3,10-difluorodibenzo(a,h)pyrene, either were inactive or exhibited (on a dose basis) a week response. However, the mutagenicity of the dibenzopyrenes was eliminated when they were coincubated with 7,8-benzoflavone, a mixed-function oxidase inhibitor. The results suggest that metabolic oxidation of these polycyclic aromatic hydrocarbons at the bay region (presumably to diol-epoxides) is required for a mutagenic response in the cell-mediated assay.

1 Research sponsored by the National Cancer Institute under Interagency Agreement 40-636-77; by the Environmental Protection Agency under Interagency Agreement 79-D-XO533 with the United States Department of Energy, under Contract W-7405-eng-26 with the Union Carbide Corporation; and by National Cancer Institute Grant CA 23454.

2 To whom requests for reprints should be addressed, at Toxicology Department, Shell Development Co., Westhollow Research Center, Box 822, Houston, Texas 77001.

3 To whom requests for reprints should be addressed, at Division of Biological and Medical Research, Argonne National Laboratory, Argonne, III. 60439.

Received 8/ 3/81. Accepted 1/28/82.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1982 by the American Association for Cancer Research.