Transformation by different oncogenes relies on specific metabolic adaptations

Cell Cycle. 2016 Oct;15(19):2656-2668. doi: 10.1080/15384101.2016.1215387. Epub 2016 Aug 2.

Abstract

Metabolic adaptations are emerging as common traits of cancer cells and tumor progression. In vitro transformation of NIH 3T3 cells allows the analysis of the metabolic changes triggered by a single oncogene. In this work, we have compared the metabolic changes induced by H-RAS and by the nuclear resident mutant of histone deacetylase 4 (HDAC4). RAS-transformed cells exhibit a dominant aerobic glycolytic phenotype characterized by up-regulation of glycolytic enzymes, reduced oxygen consumption and a defect in complex I activity. In this model of transformation, glycolysis is strictly required for sustaining the ATP levels and the robust cellular proliferation. By contrast, in HDAC4/TM transformed cells, glycolysis is only modestly up-regulated, lactate secretion is not augmented and, instead, mitochondrial oxygen consumption is increased. Our results demonstrate that cellular transformation can be accomplished through different metabolic adaptations and HDAC4/TM cells can represent a useful model to investigate oncogene-driven metabolic changes besides the Warburg effect.

Keywords: CLN3; CPT1A; ENO2; GLA; Glycolysis; HDAC4; HDAC5; HDAC7; HDAC9; HK2; MEF2A; MEF2B; MEF2C; MEF2D; NSDHL; OXPHOS; PGK1; PKM2; RHOB; Warburg; class IIa; mitochondria.

MeSH terms

  • Adaptation, Physiological*
  • Animals
  • Breast Neoplasms / genetics
  • Cell Respiration
  • Cell Transformation, Neoplastic / metabolism*
  • Electron Transport Complex I / metabolism
  • Female
  • Fibroblasts / metabolism
  • Gene Expression Regulation
  • Glycolysis
  • Histone Deacetylases / metabolism
  • Humans
  • Lactic Acid / metabolism
  • Lipid Metabolism / genetics
  • Mice
  • Mitochondria / metabolism
  • NIH 3T3 Cells
  • Oncogenes*
  • ras Proteins / metabolism

Substances

  • Lactic Acid
  • Histone Deacetylases
  • ras Proteins
  • Electron Transport Complex I