Metabolic reprogramming of cancer-associated fibroblasts by IDH3α downregulation

Cell Rep. 2015 Mar 3;10(8):1335-48. doi: 10.1016/j.celrep.2015.02.006. Epub 2015 Feb 26.

Abstract

Cancer-associated fibroblasts (CAFs) provide critical metabolites for tumor growth and undergo metabolic reprogramming to support glycolysis. However, the molecular mechanisms responsible for this change remain unclear. Here, we report that TGF-β1- or PDGF-induced CAFs switch from oxidative phosphorylation to aerobic glycolysis. We identify downregulation of isocitrate dehydrogenase 3α (IDH3α) as a marker for this switch. Furthermore, miR-424 downregulates IDH3α during CAF formation. Downregulation of IDH3α decreases the effective level of α-ketoglutarate (α-KG) by reducing the ratio of α-KG to fumarate and succinate, resulting in PHD2 inhibition and HIF-1α protein stabilization. The accumulation of HIF-1α, in turn, promotes glycolysis by increasing the uptake of glucose, upregulating expression of glycolytic enzymes under normoxic conditions, and inhibiting oxidative phosphorylation by upregulating NDUFA4L2. CAFs from tumor samples exhibit low levels of IDH3α, and overexpression of IDH3α prevents transformation of fibroblasts into CAFs. Our studies reveal IDH3α to be a critical metabolic switch in CAFs.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cells, Cultured
  • Colonic Neoplasms / metabolism
  • Colonic Neoplasms / pathology*
  • Down-Regulation* / drug effects
  • Electron Transport Complex I / metabolism
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism*
  • Glucose / metabolism
  • Glycolysis / drug effects
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Isocitrate Dehydrogenase / antagonists & inhibitors
  • Isocitrate Dehydrogenase / genetics
  • Isocitrate Dehydrogenase / metabolism*
  • Ketoglutaric Acids / metabolism
  • Metabolic Engineering*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • MicroRNAs / metabolism
  • Oxidative Phosphorylation
  • Phosphorylation
  • Platelet-Derived Growth Factor / pharmacology
  • Prolyl Hydroxylases / metabolism
  • RNA, Small Interfering / metabolism
  • Transforming Growth Factor beta1 / pharmacology
  • Up-Regulation / drug effects

Substances

  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Ketoglutaric Acids
  • MIRN424 microrna, human
  • MicroRNAs
  • Platelet-Derived Growth Factor
  • RNA, Small Interfering
  • Transforming Growth Factor beta1
  • Isocitrate Dehydrogenase
  • Prolyl Hydroxylases
  • NDUFA4L2 protein, mouse
  • Electron Transport Complex I
  • Glucose

Associated data

  • GEO/GSE61797