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[Cancer Research 27, 1587-1594, September 1, 1967]
© 1967 American Association for Cancer Research

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The Effect of Fatty Acid Structure on Utilization by Ehrlich Ascites Tumor Cells

Arthur A. Spector and Daniel Steinberg

Laboratory of Metabolism, National Heart Institute, NIH, Bethesda, Maryland 20014

The effect of fatty acid structure on utilization by Ehrlich ascites tumor cells was studied in vitro. Unesterified palmitate, stearate, oleate, and linoleate were metabolized in a qualitatively similar fashion and at roughly comparable rates. Each of these fatty acids was rapidly taken up by the cells in unesterified form. The amount of free fatty acid taken up during the first few minutes was determined by the molar ratio of fatty acid to albumin in the incubation medium and differed for each fatty acid: stearate > palmitate > oleate > linoleate. This concentration of cell-free fatty acid was then maintained with little or no further change during continued exposure for 1 hr to the same medium. On the other hand, the amounts of free fatty acid oxidized to CO2 and incorporated into lipid esters increased progressively. The rates of oxidation and esterification were related to the fatty acid-albumin molar ratio in the medium and, thus, to the steady-state concentration of free fatty acid associated with the cells. Radioactive linoleate was oxidized at a somewhat greater rate than the other long-chain free fatty acids. Acetate, ß-hydroxybutyrate, octanoate, and laurate were metabolized at considerably lower rates than the long-chain free fatty acids. Pyruvate was oxidized as rapidly as palmitate but was poorly incorporated into cell lipid. Attempts to demonstrate net utilization of lipid esters contained in Ehrlich ascites tumor fluid by the cells in vitro were negative. Radioactive palmitate contained in biologically labeled rat chylomicrons was utilized very slowly relative to unesterified palmitate. These observations support the hypothesis that exogenously supplied free fatty acid is a major source of fat for this tumor cell.

Received 1/ 4/67. Accepted 5/ 8/67.







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 Cell Growth & Differentiation
Copyright © 1967 by the American Association for Cancer Research.