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Relationship of In Vitro Toxicity of Technetium-99m to Subcellular Localisation and Absorbed Dose.

Authors :
Costa IM
Siksek N
Volpe A
Man F
Osytek KM
Verger E
Schettino G
Fruhwirth GO
Terry SYA
Source :
International journal of molecular sciences [Int J Mol Sci] 2021 Dec 15; Vol. 22 (24). Date of Electronic Publication: 2021 Dec 15.
Publication Year :
2021

Abstract

Auger electron-emitters increasingly attract attention as potential radionuclides for molecular radionuclide therapy in oncology. The radionuclide technetium-99m is widely used for imaging; however, its potential as a therapeutic radionuclide has not yet been fully assessed. We used MDA-MB-231 breast cancer cells engineered to express the human sodium iodide symporter-green fluorescent protein fusion reporter (hNIS-GFP; MDA-MB-231.hNIS-GFP) as a model for controlled cellular radionuclide uptake. Uptake, efflux, and subcellular location of the NIS radiotracer [ <superscript>99m</superscript> Tc]TcO <subscript>4</subscript> <superscript>-</superscript> were characterised to calculate the nuclear-absorbed dose using Medical Internal Radiation Dose formalism. Radiotoxicity was determined using clonogenic and γ-H2AX assays. The daughter radionuclide technetium-99 or external beam irradiation therapy (EBRT) served as controls. [ <superscript>99m</superscript> Tc]TcO <subscript>4</subscript> <superscript>-</superscript> in vivo biodistribution in MDA-MB-231.hNIS-GFP tumour-bearing mice was determined by imaging and complemented by ex vivo tissue radioactivity analysis. [ <superscript>99m</superscript> Tc]TcO <subscript>4</subscript> <superscript>-</superscript> resulted in substantial DNA damage and reduction in the survival fraction (SF) following 24 h incubation in hNIS-expressing cells only. We found that 24,430 decays/cell (30 mBq/cell) were required to achieve SF <subscript>0.37</subscript> (95%-confidence interval = [SF <subscript>0.31</subscript> ; SF <subscript>0.43</subscript> ]). Different approaches for determining the subcellular localisation of [ <superscript>99m</superscript> Tc]TcO <subscript>4</subscript> <superscript>-</superscript> led to SF <subscript>0.37</subscript> nuclear-absorbed doses ranging from 0.33 to 11.7 Gy. In comparison, EBRT of MDA-MB-231.hNIS-GFP cells resulted in an SF <subscript>0.37</subscript> of 2.59 Gy. In vivo retention of [ <superscript>99m</superscript> Tc]TcO <subscript>4</subscript> <superscript>-</superscript> after 24 h remained high at 28.0% ± 4.5% of the administered activity/gram tissue in MDA-MB-231.hNIS-GFP tumours. [ <superscript>99m</superscript> Tc]TcO <subscript>4</subscript> <superscript>-</superscript> caused DNA damage and reduced clonogenicity in this model, but only when the radioisotope was taken up into the cells. This data guides the safe use of technetium-99m during imaging and potential future therapeutic applications.

Details

Language :
English
ISSN :
1422-0067
Volume :
22
Issue :
24
Database :
MEDLINE
Journal :
International journal of molecular sciences
Publication Type :
Academic Journal
Accession number :
34948266
Full Text :
https://doi.org/10.3390/ijms222413466