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[Cancer Research 25, 1459-1462, October 1, 1965]
© 1965 American Association for Cancer Research

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Effects of 1-ß-D-Arabinofuranosylcytosine Hydrochloride on Regenerating Bone Marrow1

R. J. Papac, P. Calabresi2, J. W. Hollingsworth and A. D. Welch

Department of Medicine and Pharmacology, Yale University School of Medicine, New Haven, Connecticut

1-ß-D-Arabinofuranosylcytosine (ara-C3 or cytosine arabinoside), a pyrimidine nucleoside analog, is capable of inhibiting marrow regeneration in lethally irradiated mice in which marrow recolonization by donor marrow cells from normal mice occurs. When administered on the 4th day after irradiation and marrow injection, the drug induces significant marrow suppression. Depending upon the relative amounts of the compounds and the intervals of time between their administration, reversal of the effect of cytosine arabinoside on the bone marrow can be accomplished by deoxycytidine. When the metabolic block induced by cytosine arabinoside is circumvented by deoxycytidine, with release of the biosynthesis of DNA, the administration of certain cytotoxic agents yields enhanced suppression of the regenerating bone marrow of mice.

1 Supported by USPHS Grants CA-02817, CA-05944, CA-5138, and MO-FR38.

3 The abbreviations used are: ara-C, cytosine arabinoside (1-ß-D-arabinofuranosylcytosine hydrochloride); DNA, deoxyribonucleic acid; CdR, 2'-deoxycytidine; IUdR, 5-iodo-2'-deoxyuridine; HN2, nitrogen mustard.

2 Burroughs Wellcome Scholar in Clinical Pharmacology.

Received 12/23/64. Revised 5/13/65.





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 © 1965 by the American Association for Cancer Research.