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[Cancer Research 32, 2612-2615, December 1, 1972]
© 1972 American Association for Cancer Research

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Mechanism of 1-ß-D-Arabinofuranosylcytosine-induced Cell Lethality1

Myron Karon2, William F. Benedict and Natalie Rucker

Division of Hematology, Department of Pediatrics, Children's Hospital of Los Angeles, and the University of Southern California School of Medicine, Los Angeles, California 90054

1-ß-D-Arabinofuranosylcytosine-induced cell lethality as measured by survival fraction in a plating efficiency assay with the use of cultures of hamster fibroblasts correlates with the production of five or more chromatid breaks per metaphase. By contrast neither the degree of inhibition of DNA synthesis nor the magnitude of unbalanced growth as determined by cell sizing produced by a variety of 1-ß-D-arabinofuranosylcytosine dosages correlated with cell death. Chromatid breakage can therefore be used as a sensitive means of assessing cell cytotoxicity.

1 Supported by NIH Grants CA 11050-05 from the National Cancer Institute and T-493 from the American Cancer Society.

2 Scholar of the Leukemia Society of America, Inc.

Received 6/20/72. Accepted 8/22/72.




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S. D. Cline and N. Osheroff
Cytosine Arabinoside Lesions Are Position-specific Topoisomerase II Poisons and Stimulate DNA Cleavage Mediated by the Human Type II Enzymes
J. Biol. Chem., October 15, 1999; 274(42): 29740 - 29743.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1972 by the American Association for Cancer Research.