Exp Clin Endocrinol Diabetes 2001; Vol. 109(1): 60-62
DOI: 10.1055/s-2001-11010
Mini-Review

© Johann Ambrosius Barth

Gene therapy with sodium/iodide symporter in hepatocarcinoma

U. Haberkorn
  • Department of Nuclear Medicine, University of Heidelberg and Clinical Cooperation Unit Radiation Therapy, German Cancer Research Center, Heidelberg, Germany
Further Information

Publication History

Publication Date:
31 December 2001 (online)

Summary:

The ability of thyroid cells to accumulate iodide is a prerequisite for successfull radioiodide therapy of benign thyroid diseases and differentiated thyroid carcinoma. The transport of iodide across the cell membrane is mediated by the sodium iodide symporter (hNIS). Employing a bicistronic retroviral vector for the transfer of the hNIS coding sequence and the hygromycin resistence gene stable hNIS expressing rat Morris hepatoma (MH3924A) cell lines were generated by hygromycin selection. Genetically modified MH3924A cell lines accumulated up to 235 times more iodide when compared to non-infected hepatoma cells with a maximal iodide uptake after 60 minutes incubation. Competition experiments in the presence of sodium perchlorate revealed a dose dependent decrease of the iodide uptake, FCCP led to a loss of accumulated I-, whereas DIDS increased the I- uptake into the cells. However, a rapid efflux of the radioactivity (80%) was observed during the first 10 minutes after the 125I- containing medium had been replaced by non-radioactive medium. In rats, the hNIS-expressing tumors accumulated six times more iodide as compared to the contralateral wild type tumor as monitored by scintigraphy. An ex vivo quantitation of the iodide content performed 1 hour after tracer administration in 1g tumor tissue revealed a 17-fold higher iodide accumulation in the genetically modified tumors. In vivo also a rapid efflux of the radioactivity out of the tumor was observed. Therefore, the transduction of the hNIS gene per se is sufficient to induce 125I- transport in Morris hepatoma cells in vitro and in vivo. For a therapeutic application of the hNIS gene, however, additional conditions need to be defined which inhibit the iodide efflux.

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Prof. Dr. Uwe Haberkorn

Department of Nuclear Medicine

University of Heidelberg

Im Neuenheimer Feld 400

D-69120 Heidelberg

Germany

Phone: +49-6221-567731

Fax: +49-6221-567473

Email: Uwe_Haberkorn@med.uni-heidelberg.de

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