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 29, 1590-1597, August 1, 1969]
© 1969 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 Simard, R.
Right arrow Articles by Cassingena, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Simard, R.
Right arrow Articles by Cassingena, R.

Actinomycin Resistance in Cultured Hamster Cells

René Simard1 and Roland Cassingena

Institut de Recherches Scientifiques sur le Cancer, 94-Villejuif, France

A cell line derived from a malignant hamster tumor was made resistant to 1 µg/ml actinomycin D by continuous exposure to increasing concentrations of the antibiotic. In addition to a normal nucleolus, the resistant cells exhibited several small exhausted ones in the terminal phase of nucleolar segregation. Comparative growth rate and incorporation of uridine-3H revealed a significant delay in the resistant line as compared with the sensitive one, although the same sequence of incorporation was found qualitatively within the nucleolus and the nucleus. Cross-resistance was present in resistant cells with Nogalamycin and Chromomycin, two antibiotics with a mode of action similar to actinomycin but chemically unrelated. Incorporation of actinomycin D-3H was studied by high-resolution radioautography: radioactivity was found in the chromatin of resistant cells although in lower amounts than in sensitive cells.

According to other experiments, actinomycin penetration was thought to be altered in resistant HeLa and B. subtilis cells. In the present case, the resistance is considered likely to result from a successive derepression of secondary organizers and/or the development of an enzymatic mechanism for inacti-vation of actinomycin inside the cell.

1 Present address: Laboratoire de Biologie Moléculaire, Faculté de Médecine, Université de Sherbrooke, Sherbrooke, Canada.

Received 11/25/68. Accepted 4/10/69.







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 © 1969 by the American Association for Cancer Research.