Targeting novel sodium iodide symporter interactors ADP-ribosylation factor 4 and valosin-containing protein enhances radioiodine uptake

Alice Fletcher, Martin Read, Caitlin Thornton, Dean Larner, Vikki Poole, Kate Brookes, Hannah Nieto, Mohammed Alshahrani, Rebecca Thompson, Gareth Lavery, Iňigo Landa, James A Fagin, Moray J Campbell, Kristien Boelaert, Andrew Turnell, Vicki Smith, Christopher McCabe

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)
179 Downloads (Pure)

Abstract

The sodium iodide symporter (NIS) is required for iodide uptake which facilitates thyroid hormone biosynthesis. NIS has been exploited for over 75 years in ablative radioiodine (RAI) treatment of thyroid cancer where its ability to transport radioisotopes depends on its localization to the plasma membrane. The advent of NIS-based in vivo imaging and theranostic strategies in other malignancies and disease modalities has recently increased the clinical importance of NIS. However, NIS trafficking remains ill-defined. Here, we employed tandem mass spectrometry followed by co-immunoprecipitation and proximity ligation assays to identify and validate two key nodes - ADP-ribosylation factor 4 (ARF4) and valosin-containing protein (VCP) - controlling NIS trafficking. Using cell surface biotinylation assays and highly inclined and laminated optical sheet microscopy we demonstrated that ARF4 enhanced NIS vesicular trafficking from the Golgi to the plasma membrane, whereas VCP - a principal component of ER-associated degradation - governed NIS proteolysis. Gene expression analysis indicated VCP expression was particularly induced in aggressive thyroid cancers and in patients who had poorer outcomes following RAI treatment. Two re-purposed Food and Drug Administration (FDA)-approved VCP inhibitors abrogated VCP-mediated repression of NIS function resulting in significantly increased NIS at the cell surface and markedly increased RAI uptake in mouse and human thyroid models. Collectively, these discoveries delineate NIS trafficking and highlight the new possibility of systemically enhancing RAI therapy in patients using FDA-approved drugs.
Original languageEnglish
Pages (from-to)102–115
JournalCancer Research
Volume80
Issue number1
Early online date31 Oct 2019
DOIs
Publication statusPublished - Jan 2020

Keywords

  • NIS
  • radioiodine
  • ARF4
  • VCP
  • FDA-approved

Fingerprint

Dive into the research topics of 'Targeting novel sodium iodide symporter interactors ADP-ribosylation factor 4 and valosin-containing protein enhances radioiodine uptake'. Together they form a unique fingerprint.

Cite this