213 Bi-Labeled Prostate-Specific Membrane Antigen-Targeting Agents Induce DNA Double-Strand Breaks in Prostate Cancer Xenografts

Abstract

Background:

Up to now, prostate-specific membrane antigen (PSMA)-targeted radionuclide therapy mainly focused on β-emitting radionuclides. Herein, two new ²¹³Bi-labeled agents for PSMA-targeted α therapy of prostate cancer (PCa) are reported.

Methods:

The biodistribution of ²¹³Bi-labeled small-molecule inhibitor PSMA I&T and nanobody JVZ-008 was evaluated in mice bearing PSMA-positive LNCaP xenografts. DNA damage response was followed using LNCaP cells and LNCaP xenografts.

Results:

In vitro, ²¹³Bi-PSMA I&T and ²¹³Bi-JVZ-008 therapy of LNCaP cells led to increased number of DNA double-strand breaks (DSBs), detected as 53BP1 and γH2AX nuclear foci. In vivo, tumor uptake of ²¹³Bi-PSMA I&T and ²¹³Bi-JVZ-008 was 5.75% ± 2.70%ID/g (injected dose per gram) and 2.68% ± 0.56%ID/g, respectively, with similar tumor-to-kidney ratios. Furthermore, both agents induced in vivo DSBs in the tumors, which were detected between 1 hour and 24 hours after injection. ²¹³Bi-PSMA I&T induced significantly more DSBs than ²¹³Bi-JVZ-008 (p < 0.01).

Conclusions:

²¹³Bi-PSMA I&T and ²¹³Bi-JVZ-008 showed efficient and rapid tumor targeting and produced DSBs in PSMA-expressing LNCaP cells and xenografts. These promising results require further evaluation of ²¹³Bi-labeled agents with regard to their therapeutic efficacy and toxicity for PCa therapy.