The sodium iodide symporter (NIS): novel applications for radionuclide imaging and treatment.

C Spitzweg, P J Nelson, E Wagner, P Bartenstein, W A Weber, M Schwaiger, J C Morris

Journal: Endocrine-related cancer 2022;28(10):T193-T213

PMID: 34259647

Abstract

Cloning of the sodium iodide symporter (NIS) 25 years ago has opened an exciting chapter in molecular thyroidology with the characterization of NIS as one of the most powerful theranostic genes and the development of a promising gene therapy strategy based on image-guided selective NIS gene transfer in non-thyroidal tumors followed by application of 131I or alternative radionuclides, such as 188Re and 211At. Over the past two decades, significant progress has been made in the development of the NIS gene therapy concept, from local NIS gene delivery towards promising new applications in disseminated disease, in particular through the use of oncolytic viruses, non-viral polyplexes, and genetically engineered MSCs as highly effective, highly selective and flexible gene delivery vehicles. In addition to allowing the robust therapeutic application of radioiodine in non-thyroid cancer settings, these studies have also been able to take advantage of NIS as a sensitive reporter gene that allows temporal and spatial monitoring of vector biodistribution, replication, and elimination - critically important issues for preclinical development and clinical translation.

Address: Department of Internal Medicine IV, University Hospital of LMU Munich, Munich, Germany.; Division of Endocrinology, Diabetes, Metabolism and Nutrition, Mayo Clinic, Rochester, Minnesota, USA.; Pharmaceutical Biotechnology, Department of Pharmacy, Centre for System-Based Drug Research, and Centre for Nanoscience, LMU Munich, Munich, Germany.; Department of Nuclear Medicine, University Hospital of LMU Munich, Munich, Germany.; Department of Nuclear Medicine, Klinikum rechts der Isar, Technical University Munich, Munich, Germany.; Division of Medical Oncology, Mayo Clinic, Rochester, Minnesota, USA.

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