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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1985 Jun;82(11):3535–3538. doi: 10.1073/pnas.82.11.3535

Glycolysis and methylaminoisobutyrate uptake in rat-1 cells transfected with ras or myc oncogenes.

E Racker, R J Resnick, R Feldman
PMCID: PMC397819  PMID: 3858838

Abstract

A high rate of aerobic glycolysis was catalyzed by rat-1 cells transfected with a ras oncogene (ras cells); rat-1 cells and rat-1 cells transfected with myc oncogene (myc cells) showed a low rate of glycolysis that was increased after exposure of the cells to type B transforming growth factor (TGF-beta). The uptake of radioactive methylaminoisobutyric acid or L-methionine via system A of amino acid transport also was accelerated after exposure of these cells to TGF-beta, with the myc cells being most sensitive and the ras cells least sensitive. Methionine was found to be a potent inhibitor of glycolysis in ras cells as well as in rat-1 or myc cells that were exposed to TGF-beta. We propose a relationship between the product of the ras oncogene (p21) and the protein(s) induced by exposure to TGF-beta.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Boerner P., Resnick R. J., Racker E. Stimulation of glycolysis and amino acid uptake in NRK-49F cells by transforming growth factor beta and epidermal growth factor. Proc Natl Acad Sci U S A. 1985 Mar;82(5):1350–1353. doi: 10.1073/pnas.82.5.1350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Boerner P., Saier M. H., Jr Growth regulation and amino acid transport in epithelial cells: influence of culture conditions and transformation on A, ASC, and L transport activities. J Cell Physiol. 1982 Nov;113(2):240–246. doi: 10.1002/jcp.1041130209. [DOI] [PubMed] [Google Scholar]
  3. Christiansen R. O., Steensland H., Loyter A., Saltzgaber J., Racker E. Energy-linked ion translocation in submitochondrial particles. II. Properties of submitochondrial particles capable of Ca++ translocation. J Biol Chem. 1969 Aug 25;244(16):4428–4436. [PubMed] [Google Scholar]
  4. Gazzola G. C., Dall'Asta V., Franchi-Gazzola R., Bussolati O., Longo N., Guidotti G. G. Post-translational control by carrier availability of amino acid transport in fetal human fibroblasts. Biochem Biophys Res Commun. 1984 Apr 16;120(1):172–178. doi: 10.1016/0006-291x(84)91429-3. [DOI] [PubMed] [Google Scholar]
  5. Inman W. H., Colowick S. P. Stimulation of glucose uptake by transforming growth factor beta: evidence for the requirement of epidermal growth factor-receptor activation. Proc Natl Acad Sci U S A. 1985 Mar;82(5):1346–1349. doi: 10.1073/pnas.82.5.1346. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Isselbacher K. J. Increased uptake of amino acids and 2-deoxy-D-glucose by virus-transformed cells in culture. Proc Natl Acad Sci U S A. 1972 Mar;69(3):585–589. doi: 10.1073/pnas.69.3.585. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Jullien M., Villaudy J., Golde A., Harel L. Inhibition by quercetin of the release of density dependent-inhibition of cell growth in RSV-transformed chicken cells. Cell Biol Int Rep. 1984 Nov;8(11):939–947. doi: 10.1016/0309-1651(84)90192-9. [DOI] [PubMed] [Google Scholar]
  8. Kelley D. S., Potter V. R. Regulation of amino acid transport systems by amino acid depletion and supplementation in monolayer cultures of rat hepatocytes. J Biol Chem. 1978 Dec 25;253(24):9009–9017. [PubMed] [Google Scholar]
  9. Kelley D. S., Potter V. R. Repression, derepression, transinhibition, and trans-stimulation of amino acid transport in rat hepatocytes and four rat hepatoma cell lines in culture. J Biol Chem. 1979 Jul 25;254(14):6691–6697. [PubMed] [Google Scholar]
  10. Land H., Parada L. F., Weinberg R. A. Tumorigenic conversion of primary embryo fibroblasts requires at least two cooperating oncogenes. Nature. 1983 Aug 18;304(5927):596–602. doi: 10.1038/304596a0. [DOI] [PubMed] [Google Scholar]
  11. Racker E., Johnson J. H., Blackwell M. T. The role of ATPase in glycolysis of Ehrlich ascites tumor cells. J Biol Chem. 1983 Mar 25;258(6):3702–3705. [PubMed] [Google Scholar]
  12. Scholnick P., Lang D., Racker E. Regulatory mechanisms in carbohydrate metabolism. IX. Stimulation of aerobic glycolysis by energy-linked ion transport and inhibition by dextran sulfate. J Biol Chem. 1973 Jul 25;248(14):5175–5175. [PubMed] [Google Scholar]
  13. Stern P. H., Wallace C. D., Hoffman R. M. Altered methionine metabolism occurs in all members of a set of diverse human tumor cell lines. J Cell Physiol. 1984 Apr;119(1):29–34. doi: 10.1002/jcp.1041190106. [DOI] [PubMed] [Google Scholar]
  14. Tamanoi F., Walsh M., Kataoka T., Wigler M. A product of yeast RAS2 gene is a guanine nucleotide binding protein. Proc Natl Acad Sci U S A. 1984 Nov;81(22):6924–6928. doi: 10.1073/pnas.81.22.6924. [DOI] [PMC free article] [PubMed] [Google Scholar]

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