INPP4B-mediated tumor resistance is associated with modulation of glucose metabolism via hexokinase 2 regulation in laryngeal cancer cells

Biochem Biophys Res Commun. 2013 Oct 11;440(1):137-42. doi: 10.1016/j.bbrc.2013.09.041. Epub 2013 Sep 17.

Abstract

Inositol polyphosphate 4-phosphatase type II (INPP4B) was recently identified as a tumor resistance factor in laryngeal cancer cells. Herein, we show that INPP4B-mediated resistance is associated with increased glycolytic phenotype. INPP4B expression was induced by hypoxia and irradiation. Intriguingly, overexpression of INPP4B enhanced aerobic glycolysis. Of the glycolysis-regulatory genes, hexokinase 2 (HK2) was mainly regulated by INPP4B and this regulation was mediated through the Akt-mTOR pathway. Notably, codepletion of INPP4B and HK2 markedly sensitized radioresistant laryngeal cancer cells to irradiation or anticancer drug. Moreover, INPP4B was significantly associated with HK2 in human laryngeal cancer tissues. Therefore, these results suggest that INPP4B modulates aerobic glycolysis via HK2 regulation in radioresistant laryngeal cancer cells.

Keywords: ERK-1/2; FDG; Glycolysis; HIF-1α; HK2; INPP4B; Laryngeal cancer; PI3K; PTEN; RR-HEp-2; Tumor resistance; extracellular signal-regulated protein kinase-1/2; fluorodeoxyglucose; hexokinase 2; hypoxia-inducible factor-1α; inositol polyphosphate 4-phosphatase Type II; phosphatase and tensin homolog; phosphoinositide 3-kinases; radioresistant HEp-2; siRNA; small interfering RNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm*
  • Glucose / metabolism
  • Glycolysis
  • Hexokinase / genetics
  • Hexokinase / metabolism*
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Laryngeal Neoplasms / drug therapy*
  • Laryngeal Neoplasms / genetics
  • Laryngeal Neoplasms / pathology
  • Laryngeal Neoplasms / radiotherapy*
  • Larynx / drug effects*
  • Larynx / metabolism
  • Larynx / pathology
  • Larynx / radiation effects*
  • Phosphoric Monoester Hydrolases / genetics
  • Phosphoric Monoester Hydrolases / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism
  • RNA Interference
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Antineoplastic Agents
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Hexokinase
  • MTOR protein, human
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • Phosphoric Monoester Hydrolases
  • phosphatidylinositol-3,4-bisphosphate 4-phosphatase
  • Glucose