Inositol phosphate recycling regulates glycolytic and lipid metabolism that drives cancer aggressiveness

ACS Chem Biol. 2014 Jun 20;9(6):1340-50. doi: 10.1021/cb5001907. Epub 2014 Apr 28.

Abstract

Cancer cells possess fundamentally altered metabolism that supports their pathogenic features, which includes a heightened reliance on aerobic glycolysis to provide precursors for synthesis of biomass. We show here that inositol polyphosphate phosphatase 1 (INPP1) is highly expressed in aggressive human cancer cells and primary high-grade human tumors. Inactivation of INPP1 leads to a reduction in glycolytic intermediates that feed into the synthesis of the oncogenic signaling lipid lysophosphatidic acid (LPA), which in turn impairs LPA signaling and further attenuates glycolytic metabolism in a feed-forward mechanism to impair cancer cell motility, invasiveness, and tumorigenicity. Taken together these findings reveal a novel mode of glycolytic control in cancer cells that can serve to promote key oncogenic lipid signaling pathways that drive cancer pathogenicity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Blotting, Western
  • Carcinoma, Papillary / drug therapy
  • Carcinoma, Papillary / metabolism
  • Carcinoma, Papillary / pathology*
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cystadenocarcinoma, Serous / drug therapy
  • Cystadenocarcinoma, Serous / metabolism
  • Cystadenocarcinoma, Serous / pathology*
  • Female
  • Glycolysis / drug effects*
  • Humans
  • Inositol Phosphates / pharmacology*
  • Lipid Metabolism / drug effects*
  • Metabolome / drug effects
  • Mice
  • Mice, SCID
  • Neoplasms / drug therapy
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / metabolism
  • Ovarian Neoplasms / pathology*
  • Phosphoric Monoester Hydrolases / antagonists & inhibitors
  • Phosphoric Monoester Hydrolases / genetics
  • Phosphoric Monoester Hydrolases / metabolism*
  • RNA, Small Interfering / genetics
  • Signal Transduction / drug effects
  • Tumor Cells, Cultured

Substances

  • Inositol Phosphates
  • RNA, Small Interfering
  • Phosphoric Monoester Hydrolases
  • inositol-1,4-bisphosphate 1-phosphatase