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[Cancer Research 22, 449-455, May 1, 1962]
© 1962 American Association for Cancer Research

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The Effect of Sarcoma 180 and Other Stressing Agents upon Adrenal Nucleic Acids*

Russell Hilf, Valentina W. Cowett, Minnie L. Johnson and Aleck Borman

( Squibb Institute for Medical Research, New Brunswick, N.J.)

The effects of Sarcoma 180, heterologous tissue implantation, and daily injections of turpentine upon adrenal and liver nucleic acids were investigated. Progressive tumor growth caused an initial elevation in adrenal ribonucleic acid (RNA) which was followed by a return to control levels. Adrenal deoxyribonucleic acid (DNA) concentration was increased during most of the period of tumor growth. The combined effect, as measured by the RNA/DNA ratio, resulted in a marked decrease below the controls as tumor growth progressed. Neither of the two nonspecific stresses studied simulated the effect of tumor growth upon adrenal nucleic acids. In general, the liver nucleic acid changes paralleled those found in the adrenal, best exemplified by the RNA/DNA ratios. These results indicate that Sarcoma 180 had a rather unique effect upon adrenal nucleic acids, and these results are discussed in relationship to the other stresses studied.

* Work supported by Contract No. Sa-43-ph-2395 from the Cancer Chemotherapy National Service Center, National Cancer Institute, National Institutes of Health.

Presented in part at the 52d Annual Meeting of the American Association for Cancer Research in Atlantic City, New Jersey, April 7–9, 1961. An abstract appears in Proc. Am. Assoc. Cancer Research, 3:235, 1961.

Received 8/14/61.





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 © 1962 by the American Association for Cancer Research.