Cancer Research
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
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 43, 2622-2627, June 1, 1983]
© 1983 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gomer, C. J.
Right arrow Articles by Benedict, W. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gomer, C. J.
Right arrow Articles by Benedict, W. F.

Comparison of Mutagenicity and Induction of Sister Chromatid Exchange in Chinese Hamster Cells Exposed to Hematoporphyrin Derivative Photoradiation, Ionizing Radiation, or Ultraviolet Radiation1

Charles J. Gomer2, Natalie Rucker, Ashu Banerjee and William F. Benedict

Clayton Center for Ocular Oncology [C. J. G., N. R., W. F. B.] and Divisions of Ophthalmology [C. J. G.] and Hematology Oncology [C. J. G., A. B., W. F. B.], Childrens Hospital of Los Angeles, Los Angeles, California 90027

Cell culture studies have been performed to compare the mutagenic potential and the induction of sister chromatid exchanges for hematoporphyrin derivative photoradiation, ionizing radiation, and UV radiation. The mutation frequency in Chinese hamster ovary cells at the hypoxanthine-guanine phosphoribosyltransferase locus was measured using resistance to 6-thioguanine. Phenotypic expression time prior to mutation selection was also examined. Treatment with either X-rays or UV was effective in producing mutants resistant to 6-thioguanine, but treatment with hematoporphyrin derivative photoradiation (at comparable toxicity levels) did not induce any mutagenic activity above background levels. The hematoporphyrin derivative incubation and photosensitization conditions used in this study did induce sister chromatid exchanges at frequencies comparable to those induced by X-rays but at lower frequencies than for UV treatments.

1 This investigation was performed in conjunction with the Clayton Foundation for Research and was supported in part by USPHS Grant CA 31230 awarded by the National Cancer Institute, Department of Health and Human Services, and by American Cancer Society Research Grant IN-21-T to the LAC-USC Comprehensive Cancer Center.

2 To whom requests for reprints should be addressed, at Clayton Center for Ocular Oncology, Childrens Hospital of Los Angeles, 4650 Sunset Boulevard, Los Angeles, Calif. 90027.

Received 6/11/82. Accepted 2/25/83.







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
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1983 by the American Association for Cancer Research.