Abstract
The cellular expression of the sodium iodide symporter (NIS) has been shown to confer iodide-concentrating capacity in non-thyroid cell types. We examined the role of NIS in the uptake of the alpha-particle emitting radiohalide [(211)At]astatide in the UVW human glioma cell line transfected to express NIS. [(211)At]Astatide uptake is shown to be NIS-dependent, with characteristics similar to [(131)I]iodide uptake. These studies suggest [(211)At]astatide as a possible alternative radionuclide to [(131)I]iodide for NIS-based endoradiotherapy, and provide a model for the study of [(211)At]astatide behavior at a cellular level.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Astatine / pharmacokinetics*
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Dose-Response Relationship, Drug
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Glioma / metabolism*
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Humans
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Iodine Radioisotopes / pharmacokinetics*
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Methimazole / administration & dosage
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Perchlorates / administration & dosage
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Radiopharmaceuticals / pharmacokinetics
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Reference Values
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Reproducibility of Results
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Sensitivity and Specificity
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Sodium Compounds / administration & dosage
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Symporters / metabolism*
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Transfection
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Tumor Cells, Cultured / metabolism
Substances
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Iodine Radioisotopes
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Perchlorates
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Radiopharmaceuticals
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Sodium Compounds
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Symporters
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sodium-iodide symporter
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Methimazole
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sodium perchlorate
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Astatine