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Beyond aerobic glycolysis: transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis.

Tumor cell proliferation requires rapid synthesis of macromolecules including lipids, proteins, and nucleotides. Many tumor cells exhibit rapid glucose consumption, with most of the glucose-derived carbon being secreted as lactate despite abundant oxygen availability (the Warburg effect). Here, we used 13C NMR spectroscopy to examine the metabolism of glioblastoma cells exhibiting aerobic glycolysis. In these cells, the tricarboxylic acid (TCA) cycle was active but was characterized by an efflux of substrates for use in biosynthetic pathways, particularly fatty acid synthesis. The success of this synthetic activity depends on activation of pathways to generate reductive power (NADPH) and to restore oxaloacetate for continued TCA cycle function (anaplerosis). Surprisingly, both these needs were met by a high rate of glutamine metabolism. First, conversion of glutamine to lactate (glutaminolysis) was rapid enough to produce sufficient NADPH to support fatty acid synthesis. Second, despite substantial mitochondrial pyruvate metabolism, pyruvate carboxylation was suppressed, and anaplerotic oxaloacetate was derived from glutamine. Glutamine catabolism was accompanied by secretion of alanine and ammonia, such that most of the amino groups from glutamine were lost from the cell rather than incorporated into other molecules. These data demonstrate that transformed cells exhibit a high rate of glutamine consumption that cannot be explained by the nitrogen demand imposed by nucleotide synthesis or maintenance of nonessential amino acid pools. Rather, glutamine metabolism provides a carbon source that facilitates the cell's ability to use glucose-derived carbon and TCA cycle intermediates as biosynthetic precursors.

Pubmed ID: 18032601

Authors

  • DeBerardinis RJ
  • Mancuso A
  • Daikhin E
  • Nissim I
  • Yudkoff M
  • Wehrli S
  • Thompson CB

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Data

December 4, 2007

Associated Grants

  • Agency: NIDDK NIH HHS, Id: K08 DK072565
  • Agency: NCI NIH HHS, Id: P01 CA104838
  • Agency: NIGMS NIH HHS, Id: T32 GM008638

Mesh Terms

  • Aerobiosis
  • Brain Neoplasms
  • Cell Line, Tumor
  • Cell Proliferation
  • Cell Transformation, Neoplastic
  • Citric Acid Cycle
  • Glioblastoma
  • Glucose
  • Glutamine
  • Glycolysis
  • Humans
  • Nucleotides
  • Protein Biosynthesis