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Metabolic changes associated with tumor metastasis, part 1: tumor pH, glycolysis and the pentose phosphate pathway

Journal

CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 73, Issue 7, Pages 1333-1348

Publisher

SPRINGER BASEL AG
DOI: 10.1007/s00018-015-2098-5

Keywords

Tumor metastasis; Tumor pH; Glycolysis; Phosphoglucose isomerase (PGI); Lactate; Pentose phosphate pathway (PPP)

Funding

  1. European Research Council (ERC) [243188 TUMETABO]
  2. Interuniversity Attraction Pole (IAP) grant from the Belgian Science Policy Office (Belspo) [UP7-03]
  3. Action de Recherche Concertee from the Communaute Francaise de Belgique [ARC 14/19-058]
  4. Belgian Fonds National de la Recherche Scientifique (F.R.S.-FNRS)
  5. Televie
  6. Belgian Fondation contre le Cancer [2012-186]
  7. Belgian Federal Agency for Nuclear Control (FANC-AFCN)
  8. Louvain Foundation
  9. UCL Fonds Speciaux de la Recherche (FSR)
  10. Belgian Nuclear Research Center (SCK.CEN)

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Metabolic adaptations are intimately associated with changes in cell behavior. Cancers are characterized by a high metabolic plasticity resulting from mutations and the selection of metabolic phenotypes conferring growth and invasive advantages. While metabolic plasticity allows cancer cells to cope with various microenvironmental situations that can be encountered in a primary tumor, there is increasing evidence that metabolism is also a major driver of cancer metastasis. Rather than a general switch promoting metastasis as a whole, a succession of metabolic adaptations is more likely needed to promote different steps of the metastatic process. This review addresses the contribution of pH, glycolysis and the pentose phosphate pathway, and a companion paper summarizes current knowledge regarding the contribution of mitochondria, lipids and amino acid metabolism. Extracellular acidification, intracellular alkalinization, the glycolytic enzyme phosphoglucose isomerase acting as an autocrine cytokine, lactate and the pentose phosphate pathway are emerging as important factors controlling cancer metastasis.

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