Cancer Research CTRC-AACR San Antonio Breast Cancer Symposium
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 25, 1463-1467, October 1, 1965]
© 1965 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 Donisch, V.
Right arrow Articles by Rossiter, R. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Donisch, V.
Right arrow Articles by Rossiter, R. J.

Metabolism of Phospholipids in Ehrlich Ascites Tumor1

V. Donisch2 and R. J. Rossiter

Department of Biochemistry, University of Western Ontario, London, Canada

When Ehrlich ascites cells were incubated in a suitable medium containing one of a number of 14C-labeled phospholipid precursors, radioactivity was recovered from the lipid fraction. For the same concentration and specific radioactivity of precursor, the incorporation was in the following order: choline-1,2-14C > ethanolamine-1,2-14C > L-serine-14C > glycerol-1-14C > formate-14C > acetate-1-14C.

Radioactivity from choline-1,2-14C was incorporated into the 3 choline-containing phospholipids—lecithin, choline plasmalogen, and sphingomyelin. Radioactivity from ethanolamine-1,2-14C was incorporated into phosphatidyl ethanolamine, ethanolamine plasmalogen, choline plasmalogen, and lecithin. Radioactivity from L-serine-14C was incorporated into phosphatidyl serine, serine plasmalogen, and sphingomyelin, and also into phosphatidic acid and other glycerophosphatides. Radioactivity from glycerol-1-14C was incorporated into phosphatidic acid and the glycerophosphatides, and also into sphingomyelin. Radioactivity from formate-14C was incorporated into phosphatidyl serine, serine plasmalogen and sphingomyelin, with lesser amounts into other phosphatides. With acetate-1-14C, radioactivity was poorly incorporated into the phosphatides of this tissue.

These results are discussed in relation to current knowledge concerning the biosynthesis of phosphatides. Evidence is given to support the following generalizations concerning the metabolism of phospholipids in the Ehrlich ascites tumor: (a) The cytosine nucleotide pathway for the biosynthesis of glycerophosphatides is operative. (b) Lipid ethanolamine is methylated to form lipid choline. (c) Phosphatidyl serine is not decarboxylated to yield phosphatidyl ethanolamine.

1 This investigation was supported by grants from the National Cancer Institute and Medical Research Council of Canada.

2 Fellow, National Cancer Institute of Canada.

Received 2/26/65. Revised 6/ 6/65.





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 © 1965 by the American Association for Cancer Research.