Cancer Research AACR Conference on Molecular Diagnostics - 2008  Tumor Immunology: New Perspectives
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 26, 1839-1846, September 1, 1966]
© 1966 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 Zischka, R.
Right arrow Articles by Beard, J. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zischka, R.
Right arrow Articles by Beard, J. W.

Effects of Actinomycin D on Avian Myeloblast and BAI Strain A Virus RNA Synthesis in Vitro1

Rosemarie Zischka, A. J. Langlois, P. R. Rao, R. A. Bonar and J. W. Beard

Department of Surgery, Duke University Medical Center, Durham, North Carolina

Avian myeloblasts infected with BAI strain A avian tumor virus were cultured in vitro and treated with actinomycin D. The effects of the drug on cell growth and death and the synthesis of cell and virus RNA were examined. Actinomycin D (AD) concentrations of 0.01–0.05 µg/ml caused cell damage and death at proportional rates, and, as shown in earlier work, inhibited cell RNA synthesis up to 60% without depressing virus RNA synthesis or virus particle liberation. In comparison, 0.5 µg AD/ml caused more rapid cell death with parallel inhibition of 70–85% of cell RNA synthesis and 70% of virus RNA synthesis but did not decrease the output of particles having the characteristic virus adenosinetriphosphatase activity. These results are discussed and compared with findings with other virus-host systems.

1 This work was aided by a research grant (C-4572) to Duke University from the National Cancer Institute, NIH, USPHS; by a grant from the American Cancer Society, Inc. (E-84A); and by the Dorothy Beard Research Fund.

Received 2/ 7/66.





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 © 1966 by the American Association for Cancer Research.