Specific Binding and Uptake of 131I-MIBG and 111In-Octreotide in Metastatic Paraganglioma – Tools for Choice of Radionuclide Therapy

J. Spetz; J. Dalmo; O. Nilsson; B. Wängberg; H. Ahlman; E. Forssell-Aronsson

doi:10.1055/s-0032-1311603

Hormone and Metabolic Research, Table of Contents

Horm Metab Res 2012; 44(05): 400-404
DOI: 10.1055/s-0032-1311603

Original Basic

Specific Binding and Uptake of ¹³¹I-MIBG and ¹¹¹In-Octreotide in Metastatic Paraganglioma – Tools for Choice of Radionuclide Therapy

J. Spetz

¹Department of Radiation Physics, Sahlgrenska Cancer Center, University of Gothenburg, Göteborg, Sweden

,

J. Dalmo

¹Department of Radiation Physics, Sahlgrenska Cancer Center, University of Gothenburg, Göteborg, Sweden

,

O. Nilsson

²Department of Pathology, Sahlgrenska Cancer Center, University of Gothenburg, Göteborg, Sweden

,

B. Wängberg

³Department of Surgery, Sahlgrenska Cancer Center, University of Gothenburg, Göteborg, Sweden

,

H. Ahlman

³Department of Surgery, Sahlgrenska Cancer Center, University of Gothenburg, Göteborg, Sweden

,

E. Forssell-Aronsson

¹Department of Radiation Physics, Sahlgrenska Cancer Center, University of Gothenburg, Göteborg, Sweden

› Author Affiliations

Abstract

Tumor-specific uptake of the radiolabeled norepinephrine analogue meta-iodobenzylguanidine via norepinephrine transporter or radiolabeled somatostatin analogues octreotide/octreotate via somatostatin receptors offers possibilities to diagnose and treat metastatic pheochromocytoma/paraganglioma. High uptake of ¹²³I-meta-iodobenzylguanidine is dependent on high expression of vesicular monoamine transporters responsible for mediating uptake of biogenic amines into dense core granules. A patient with metastatic paraganglioma (liver and bone metastases) underwent surgical removal of the primary after injection of ¹³¹I-meta-iodobenzylguanidine and ¹¹¹In-octreotide. Radioactivity was determined in biopsies from tumor and normal tissue biopsies. The tumor/blood concentration value was high: 180 for ¹³¹I-meta-iodobenzylguanidine 3 h after injection and 590 for ¹¹¹In-octreotide 27 h after injection. Studies of primary tumor cell cultures demonstrated increased cell membrane binding and internalization over time for ¹³¹I-meta-iodobenzylguanidine. The vesicular monoamine transporter antagonist reserpine and the norepinephrine transporter inhibitor clomipramine reduced internalization by 90% and 70%, respectively, after 46 h of incubation. The results demonstrated increased cell membrane binding and internalization over time also for ¹¹¹In-octreotide. Internalization was highest for a low concentration of ¹¹¹In-octreotide. Excess of octreotide reduced internalization of ¹¹¹In-octreotide with 75% after 46 h of incubation. In conclusion, uptake and tumor/blood concentration values of radiolabeled meta-iodobenzylguanidine and somatostatin analogues can be determined for metastatic pheochromocytoma/paraganglioma to evaluate the possibility to use one or both agents for therapy. For this patient, the high tumor/blood values clearly demonstrated that therapy using both radiopharmaceuticals would be most beneficial. In vitro studies verified specific cell-membrane binding and internalization in tumor cells of both radiopharmaceuticals.

Key words

norepinephrine transporter - VMAT - clomipramine - reserpine - somatostatin receptors - octreotate

Full Text

References

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