Cancer Research Translational Cancer Medicine 2008: Cancer Clinical Trials and Personalized Medicine  Susan G. Komen for the Cure-AACR Outstanding Investigator Award for Breast 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 Cell Growth & Differentiation

[Cancer Research 24, 1918-1925, December 1, 1964]
© 1964 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 Frei, E.
Right arrow Articles by Ben, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Frei, E., III
Right arrow Articles by Ben, M.

The Stathmokinetic Effect of Vincristine

Emil Frei, III, Jacqueline Whang, Robert B. Scoggins*, Eugene J. Van Scott, David P. Rall and Max Ben{dagger}

( National Cancer Institute, National Institutes of Health, Bethesda, Maryland)

A single dose of vincristine produced an increase in the mitotic index in the marrow, duodenum, and hair follicle of the rat and in the marrow, hair root, and malignant tumors of man. This increase in mitotic index resulted from "arrest" of cells in metaphase; other stages of mitosis were not increased, and post-metaphase stages decreased during vincristine effect. This mitotic "arrest" may be associated with cell death as evidenced by a quantitative decrease in cellularity of the rat bone marrow following administration of vincristine.

For all the above tissues the increase in mitotic index was linear for at least the first 6 hours after vincristine and reached a peak at approximately 12 hours. There was an inverse correlation between the magnitude of the mitotic index increase and the generation time for the various tissues. This mitotic effect does not relate regularly to the toxic effect. For example, vincristine and vinblastine produced comparable marrow mitotic "arrest" in man, whereas leukopenia occurred regularly only with vinblastine.

The interrelationships and implications of these findings are discussed.

* Massachusetts General Hospital, Boston, Mass.

{dagger} Hazleton Laboratories, Falls Church, Va.

Received 5/25/64.





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 Cell Growth & Differentiation
Copyright © 1964 by the American Association for Cancer Research.