Overexpression of SphK2 contributes to ATRA resistance in colon cancer through rapid degradation of cytoplasmic RXRα by K48/K63-linked polyubiquitination

Oncotarget. 2017 Jun 13;8(24):39605-39617. doi: 10.18632/oncotarget.17174.

Abstract

The resistance mechanisms that limit the efficacy of retinoid therapy in cancer are poorly understood. Sphingosine kinase 2 (SphK2) is a highly conserved enzyme that is mainly located in the nucleus and endoplasmic reticulum. Unlike well-studied sphingosine kinase 1 (SphK1) located in the cytosol, little has yet understood the functions of SphK2. Here we show that SphK2 overexpression contributes to the resistance of all-trans retinoic acid (ATRA) therapy in colon cancer through rapid degradation of cytoplasmic retinoid X receptor α (RXRα) by lysine 48 (K48)- and lysine 63 (K63)-based polyubiquitination. Human colonic adenocarcinoma HCT-116 cells transfected with SphK2 (HCT-116Sphk2 cells) demonstrate resistance to ATRA therapy as determined by in vitro and in vivo assays. Sphk2 overexpression increases the ATRA-induced nuclear RXRα export to cytoplasm and then rapidly degrades RXRα through the polyubiquitination pathway. We further show that Sphk2 activates the ubiquitin-proteasome system through the signal mechanisms of (1) K48-linked proteosomal degradation and (2) K63-linked ubiquitin-dependent autophagic degradation. These results provide new insights into the biological functions of Sphk2 and the molecular mechanisms that underlie the Sphk2-mediated resistance to retinoid therapy.

Keywords: cytoplasmic RXRα; polyubiquitination; retinoid therapy resistance; sphingosine kinase 2 (SphK2).

MeSH terms

  • Animals
  • Autophagy
  • Colonic Neoplasms / drug therapy
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • Disease Models, Animal
  • Drug Resistance, Neoplasm / genetics*
  • Gene Expression*
  • HCT116 Cells
  • Humans
  • Ligands
  • Mice
  • Phosphotransferases (Alcohol Group Acceptor) / genetics*
  • Protein Binding
  • Protein Transport
  • Proteolysis / drug effects
  • Retinoid X Receptor alpha / metabolism*
  • Tretinoin / pharmacology*
  • Tumor Burden / drug effects
  • Ubiquitination / drug effects
  • Ubiquitins / metabolism
  • Xenograft Model Antitumor Assays

Substances

  • Ligands
  • Retinoid X Receptor alpha
  • Ubiquitins
  • Tretinoin
  • Phosphotransferases (Alcohol Group Acceptor)
  • sphingosine kinase 2, human