Comparison of the Radiotoxicity of Two Alpha-Particle-Emitting Immunoconjugates, Terbium-149 and Bismuth-213, Directed against a Tumor-Specific, Exon 9 Deleted (d9) E-Cadherin Adhesion Protein
Autor: | Matthias Miederer, Christof Seidl, Jozef J. Comor, Karl-Friedrich Becker, Roswitha Huber, Reingard Senekowitsch-Schmidtke, Sanja Vranjes-Duric, D. E. Charlton, Gerd-Jurgen Beyer, Christoph Schuhmacher, Christos Apostolidis, Tuomo Nikula |
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Rok vydání: | 2003 |
Předmět: |
Cell Survival
medicine.drug_class Biophysics Biology medicine.disease_cause Monoclonal antibody Exon Neoplasms medicine Humans Radiology Nuclear Medicine and imaging Binding site Terbium Mutation Radiation Cadherin Exons Adhesion Transfection Radioimmunotherapy Alpha Particles Cadherins Molecular biology 3. Good health Cancer cell Bismuth Gene Deletion |
Zdroj: | Radiation Research |
ISSN: | 1938-5404 0033-7587 |
DOI: | 10.1667/0033-7587(2003)159[0612:cotrot]2.0.co;2 |
Popis: | We investigated the effects of the a-particle emitters Tb-149 and Bi-213 coupled to a tumor-specific antibody targeting the mutated delta 9 E-cadherin (d9 E-Cad) on single cells and cell pellets. The d9 mutation of the adhesion molecule E-cadherin is found in 10% of diffuse-type gastric cancers and is not expressed in normal tissue. Human breast cancer cells (MDA-MB-435S) transfected with d9 E-Cad or the wild-type E-cadherin gene were used to study the effects of anti-d9 E-Cad MAb coupled to Tb-149 and Bi-213 (Tb-149-d9 MAb and Bi-213-d9 MAb). The density of binding sites determined on transfected MDA tumor cells by Scatchard analysis and flow cytometry varied from 4 x 10(4) to 6 x 10(4) antigens per cell. Internalization of radioimmunoconjugates by cells expressing d9 E-Cad was less than 10% of bound antibody within 240 min. The effect of the radioimmunoconjugates on cell suspensions and cell pellets was quantified by [H-3]thymidine incorporation, and the dose to the cell nuclei was determined using microdosimetric calculations. Tb-149 and Bi-213 immunoconjugates affected cells in suspension similarly. Significant differences in the proliferation capacity of d9 E-cadherin- and wildtype E-cadherin-expressing cells were observed at activity concentrations around 185 kBq/ml, corresponding to antibody concentrations between 200 ng/ml and 1000 ng/ml. Proliferation after incubation with Bi-213-d9 MAb was 50% greater in pelleted wild-type E-Cad-expressing cells compared to wildtype E-Cad cells in suspension. In contrast, the proliferation of pelleted d9 E-Cad cells was similar to that of d9 E-Cad cells in suspension. For Tb-149-d9 MAb, no significant difference was found between pelleted cells and cells in suspension for low activity concentrations. However, at high activity concentrations, Tb-149-d9 MAb had only a small effect on pelleted cells. These in vitro studies demonstrate different effects of Tb-149 and Bi-213 conjugated to a tumor-specific antibody toward single cells and tumor cell pellets. Microdosimetric simulation of single cell survival after a-particle irradiation modeled the experimental results with reasonable accuracy. (C) 2003 by Radiation Research Society. |
Databáze: | OpenAIRE |
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