Literature DB >> 165343

Lipids of cultured hepatoma cells. VI. Glycerolipid and monoenoic fatty acid biosynthesis in minimal deviation hepatoma 7288C-1.

R D Wiegand, R Wood.   

Abstract

1-14C-Acetic, 1-14C-palmitic, or 1-14C-stearic acid was incubated with minimal deviation hepatoma 7288C cells grown in culture to assess: de novo fatty acid synthesis, oxidation, desaturation, and elongation of saturated fatty acids, as well as the ability of media fatty acids to serve as precursors of cellular glycerolipids. Distribution of radioactivity in the individual lipid classes and the various fatty acids of triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine was determined. The radioactivity among the monoenoic acid isomers derived from triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine was analyzed by reductive ozonolysis. Only small amounts of the labeled substrates were oxidized to carbon dioxide. Except for labeled stearic acid, which also was incorporated heavily into phosphatidyl inositol and phosphatidyl serine, most radioactivity was recovered in triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine. Synthesis of cholesterol and long chain fatty acids from labeled acetic acid demonstrated that these cells can perform de novo synthesis of fatty acids and cholesterol. Both labeled palmitic and stearic acids were desaturated to the corresponding delta9 monoenes, and palmitic and palmitoleic acids were elongated. The nexadecenoic acid fraction isolated from triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine, when acetic or palmitic acid was the labeled substrate, showed that greater than 70 percent of the labeled acids were the delta9 isomer. Radioactivity of the octadecenoic acid fraction derived from labeled acetic or palmitic acids was nearly equally divided between the delta9 isomer, oleic acid, and the delta11 isomer, vaccenic acid. Desaturation of labeled stearic acid produced only oleic acid. These data demonstrate that the biosynthesis of vaccenic acid in these cultured neoplastic cells proceeds via the elongation of palmitoleic acid. The relatively high level of vaccenic acid synthesis in these cells suggests that the reported elevation of "oleic acid" in many neoplasms may result from increased concentration of vaccenic acid.

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Year:  1975        PMID: 165343     DOI: 10.1007/bf02534159

Source DB:  PubMed          Journal:  Lipids        ISSN: 0024-4201            Impact factor:   1.880


  12 in total

1.  A rapid method of total lipid extraction and purification.

Authors:  E G BLIGH; W J DYER
Journal:  Can J Biochem Physiol       Date:  1959-08

2.  Investigation on lipid separation methods. Separation of phospholipids from neutral fat and fatty acids.

Authors:  B BORGSTROM
Journal:  Acta Physiol Scand       Date:  1952-06-06

3.  Lipids of cultured hepatoma cells. 3. Triglyceride and phosphoglyceride biosynthesis in minimal deviation hepatoma 7288C.

Authors:  R D Wiegand; R Wood
Journal:  Lipids       Date:  1974-03       Impact factor: 1.880

4.  Lipid metabolism in cultured cells. XI. Utilization of serum triglycerides.

Authors:  J M Bailey; B V Howard; S F Tillman
Journal:  J Biol Chem       Date:  1973-02-25       Impact factor: 5.157

5.  Tumor lipids. Biosynthesis of plasmalogens.

Authors:  R Wood; K Healy
Journal:  J Biol Chem       Date:  1970-05-25       Impact factor: 5.157

6.  Conversions of palmitic and stearic acid in the intact rat.

Authors:  J Elovson
Journal:  Biochim Biophys Acta       Date:  1965-10-04

7.  [On polyenoic fatty acid and phospholipid synthesis in the tissue culture of HeLa cells].

Authors:  W Stoffel; A Scheid
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1967-02

8.  Lipids of cultured hepatoma cells. II. Effect of media lipids on cellular phospholipids.

Authors:  R Wood; J Falch
Journal:  Lipids       Date:  1973-12       Impact factor: 1.880

9.  Lipids of cultured hepatoma cells. I. Effect of serum lipid levels on cell and media lipids.

Authors:  R Wood
Journal:  Lipids       Date:  1973-12       Impact factor: 1.880

10.  Lipids of cultured hepatoma cells: V. Distribution of isomeric monoene fatty acids in individual lipid classes.

Authors:  R Wood; J Falch; R D Wiegand
Journal:  Lipids       Date:  1974-12       Impact factor: 1.880

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  15 in total

1.  Effect of dietary cyclopropene fatty acids on the octadecenoates of individual lipid classes of rat liver and hepatoma.

Authors:  R Wood; F Chumbler; R D Wiegand
Journal:  Lipids       Date:  1978-04       Impact factor: 1.880

2.  Analysis of the stearoyl-CoA desaturase system in the Morris hepatoma 7288C and 7288CTC.

Authors:  R A Zoeller; R Wood
Journal:  Lipids       Date:  1984-07       Impact factor: 1.880

3.  Effect of methyl 2-hexadecynoate on hepatic fatty acid metabolism.

Authors:  R Wood; T Lee; H Gershon
Journal:  Lipids       Date:  1980-03       Impact factor: 1.880

4.  Effect of 2-hexadecynoic acid on cultured 7288C hepatoma cells.

Authors:  G C Upreti; M Matocha; R Wood
Journal:  Lipids       Date:  1981-05       Impact factor: 1.880

5.  Geometrical and positional isomer content of the monounsaturated fatty acids from various rat tissues.

Authors:  R Wood; F Chumbler; M Matocha; A Zoeller
Journal:  Lipids       Date:  1979-09       Impact factor: 1.880

6.  Occurrence of unusual hexadecenoate fatty acids in hepatoma lipids.

Authors:  R Wood; T Lee
Journal:  Lipids       Date:  1980-10       Impact factor: 1.880

7.  Lipids of cultured hepatoma cells: VIII. Utilization of D-[1-14C] glucose for lipid biosynthesis.

Authors:  C L Welch; R Wood
Journal:  Lipids       Date:  1977-03       Impact factor: 1.880

8.  Incorporation and metabolism of stearic, oleic, linoleic and alpha-linolenic acids in minimal deviation hepatoma 7288 C cells.

Authors:  G Gaspar; M J de Alaniz; R R Brenner
Journal:  Mol Cell Biochem       Date:  1977-07-05       Impact factor: 3.396

9.  Changes in host animal plasma lipids during hepatoma growth.

Authors:  M Matocha; R Wood
Journal:  Lipids       Date:  1980-06       Impact factor: 1.880

10.  Effect of hepatoma on host liver, heart and lung lipids as tumor growth progresses.

Authors:  R Wood; A Zoeller; M Matocha
Journal:  Lipids       Date:  1982-11       Impact factor: 1.880

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