Cancer Research CR  Sign up for Cancer Research eTOC's
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, 536-541, March 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 Email this article to a friend
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 Gantt, R.
Right arrow Articles by Evans, V. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gantt, R.
Right arrow Articles by Evans, V. J.

Comparison of Soluble RNA Methylase Capacity in Paired Neoplastic and Nonneoplastic Cell Lines in Vitro

R. Gantt and V. J. Evans

Tissue Culture Section, Laboratory of Biology, National Cancer Institute, Bethesda, Maryland 20014

The RNA methylase capacity of an in vitro long-term nonneoplastic cell line was compared with an in vitro neoplastic subline. A second comparison was made with tumor tissue arising from another subline of cells implanted into syngeneic animals. Cell-free extracts of the neoplastic tissue cultured cells and the tumor tissue both had a much greater capacity to transfer methyl groups from S-adenosylmethionine to Escherichia coli soluble RNA than the tissue cultured nonneoplastic control line. This indicates a qualitative difference in the RNA methylase complements of the neoplastic and nonneoplastic cell lines. These results support the hypothesis that aberrant alkylation of nucleic acids may be a necessary chemical event in some types of neoplasia and extend the experimental evidence to an established in vitro system. In addition, with this in vitro system it is now possible to study the relationship of nucleic acid methylation to oncogenesis where the nonneoplastic controls can be maintained viable throughout the experiment for comparison with the related neoplastic line.

Received 8/ 2/68. Accepted 11/ 9/68.







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.