A novel mechanism of sodium iodide symporter repression in differentiated thyroid cancer

J Cell Sci. 2009 Sep 15;122(Pt 18):3393-402. doi: 10.1242/jcs.045427. Epub 2009 Aug 25.

Abstract

Differentiated thyroid cancers and their metastases frequently exhibit reduced iodide uptake, impacting on the efficacy of radioiodine ablation therapy. PTTG binding factor (PBF) is a proto-oncogene implicated in the pathogenesis of thyroid cancer. We recently reported that PBF inhibits iodide uptake, and have now elucidated a mechanism by which PBF directly modulates sodium iodide symporter (NIS) activity in vitro. In subcellular localisation studies, PBF overexpression resulted in the redistribution of NIS from the plasma membrane into intracellular vesicles, where it colocalised with the tetraspanin CD63. Cell-surface biotinylation assays confirmed a reduction in plasma membrane NIS expression following PBF transfection compared with vector-only treatment. Coimmunoprecipitation and GST-pull-down experiments demonstrated a direct interaction between NIS and PBF, the functional consequence of which was assessed using iodide-uptake studies in rat thyroid FRTL-5 cells. PBF repressed iodide uptake, whereas three deletion mutants, which did not localise within intracellular vesicles, lost the ability to inhibit NIS activity. In summary, we present an entirely novel mechanism by which the proto-oncogene PBF binds NIS and alters its subcellular localisation, thereby regulating its ability to uptake iodide. Given that PBF is overexpressed in thyroid cancer, these findings have profound implications for thyroid cancer ablation using radioiodine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Caveolins / metabolism
  • Cell Differentiation*
  • Cell Line
  • Gene Deletion
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Iodides / metabolism
  • Membrane Proteins / metabolism
  • Platelet Membrane Glycoproteins / metabolism
  • Protein Binding
  • Protein Transport
  • Proto-Oncogene Mas
  • Rats
  • Repressor Proteins / metabolism*
  • Subcellular Fractions / metabolism
  • Symporters / metabolism*
  • Tetraspanin 30
  • Thyroid Neoplasms / metabolism*
  • Thyroid Neoplasms / pathology*

Substances

  • Antigens, CD
  • CD63 protein, human
  • Caveolins
  • Cd63 protein, rat
  • Intracellular Signaling Peptides and Proteins
  • Iodides
  • MAS1 protein, human
  • Membrane Proteins
  • PTTG1IP protein, human
  • Platelet Membrane Glycoproteins
  • Proto-Oncogene Mas
  • Repressor Proteins
  • Symporters
  • Tetraspanin 30
  • sodium-iodide symporter