We investigated the effects of the alpha-particle emitters (149)Tb and (213)Bi 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 (149)Tb and (213)Bi ((149)Tb-d9 MAb and (213)Bi-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 [(3)H]
thymidine incorporation, and the dose to the cell nuclei was determined using microdosimetric calculations. (149)Tb and (213)Bi
immunoconjugates affected cells in
suspension similarly. Significant differences in the proliferation capacity of d9
E-cadherin- and wild-type
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 (213)Bi-d9 MAb was 50% greater in pelleted wild-type E-Cad-expressing cells compared to wild-type 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 (149)Tb-d9 MAb, no significant difference was found between pelleted cells and cells in
suspension for low activity concentrations. However, at high activity concentrations, (149)Tb-d9 MAb had only a small effect on pelleted cells. These in vitro studies demonstrate different effects of (149)Tb and (213)Bi conjugated to a
tumor-specific antibody toward single cells and
tumor cell pellets. Microdosimetric simulation of single cell survival after alpha-particle irradiation modeled the experimental results with reasonable accuracy.