FXYD6: a novel therapeutic target toward hepatocellular carcinoma

Protein Cell. 2014 Jul;5(7):532-43. doi: 10.1007/s13238-014-0045-0. Epub 2014 Apr 10.

Abstract

FXYD6, FXYD domain containing ion transport regulator 6, has been reported to affect the activity of Na(+)/K(+)-ATPase and be associated with mental diseases. Here, we demonstrate that FXYD6 is up-regulated in hepatocellular carcinoma (HCC) and enhances the migration and proliferation of HCC cells. Up-regulation of FXYD6 not only positively correlates with the increase of Na(+)/K(+)-ATPase but also coordinates with the activation of its downstream Src-ERK signaling pathway. More importantly, blocking FXYD6 by its functional antibody significantly inhibits the growth potential of the xenografted HCC tumors in mice, indicating that FXYD6 represents a potential therapeutic target toward HCC. Altogether, our results establish a critical role of FXYD6 in HCC progression and suggest that the therapy targeting FXYD6 can benefit the clinical treatment toward HCC patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology*
  • Antineoplastic Agents / pharmacology*
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / metabolism
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Female
  • HEK293 Cells
  • Humans
  • Ion Channels / antagonists & inhibitors
  • Ion Channels / metabolism*
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / metabolism
  • Mice, Inbred BALB C
  • Mice, Nude
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Tumor Burden / drug effects
  • Xenograft Model Antitumor Assays

Substances

  • Antibodies, Monoclonal
  • Antineoplastic Agents
  • FXYD6 protein, human
  • Ion Channels
  • Sodium-Potassium-Exchanging ATPase