Cancer Research Landon Prizes for Basic and Translational Cancer Research  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 30, 1773-1781, June 1, 1970]
© 1970 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 Anderson, T. J.
Right arrow Articles by Burdon, R. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Anderson, T. J.
Right arrow Articles by Burdon, R. H.

N-Methyl-N'-nitro-N-nitrosoguanidine: Reactions of Possible Significance to Biological Activity with Mammalian Cells

Thomas J. Anderson1 and Roy H. Burdon

Department of Biochemistry, University of Glasgow, Glasgow, Scotland

Mammalian cells exposed to N-methyl-N'-nitro-N-nitrosoguanidine show an immediate inhibition of DNA, RNA, and protein synthesis, as judged by radioactive precursor incorporation. DNA synthesis as determined by thymidine-3H uptake is most sensitive in this respect. The inhibition is not due to impaired uptake or phosphorylation of precursor. Studies at the enzyme level show DNA polymerase to be inhibited by N-methyl-N'-nitro-N-nitrosoguanidine in a dose-dependent manner. Experiments with exogenous thiols indicate that thiol groups of DNA polymerase may be targets for reaction with the guanidino radical resulting from N-methyl-N'-nitro-N-nitrosoguanidine decomposition. Further studies suggest that these and other groups possibly involved in substrate binding may be altered and that enzyme kinetics favor a mixed mode of enzyme inhibition.

1 Recipient of a Research Grant from the Scottish Home and Health Department. Present address: Department of Pathology, Royal Infirmary, Glasgow, Scotland.

Received 11/20/69. Accepted 2/12/70.







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 © 1970 by the American Association for Cancer Research.