Theranostic PSMA ligands with optimized backbones for intraoperative multimodal imaging and photodynamic therapy of prostate cancer

Eur J Nucl Med Mol Imaging. 2022 Jun;49(7):2425-2435. doi: 10.1007/s00259-022-05685-0. Epub 2022 Jan 14.

Abstract

Introduction: The first generation ligands for prostate-specific membrane antigen (PSMA)-targeted radio- and fluorescence-guided surgery followed by adjuvant photodynamic therapy (PDT) have already shown the potential of this approach. Here, we developed three new photosensitizer-based dual-labeled PSMA ligands by crucial modification of existing PSMA ligand backbone structures (PSMA-1007/PSMA-617) for multimodal imaging and targeted PDT of PCa.

Methods: Various new PSMA ligands were synthesized using solid-phase chemistry and provided with a DOTA chelator for 111In labeling and the fluorophore/photosensitizer IRDye700DX. The performance of three new dual-labeled ligands was compared with a previously published first-generation ligand (PSMA-N064) and a control ligand with an incomplete PSMA-binding motif. PSMA specificity, affinity, and PDT efficacy of these ligands were determined in LS174T-PSMA cells and control LS174T wildtype cells. Tumor targeting properties were evaluated in BALB/c nude mice with subcutaneous LS174T-PSMA and LS174T wildtype tumors using µSPECT/CT imaging, fluorescence imaging, and biodistribution studies after dissection.

Results: In order to synthesize the new dual-labeled ligands, we modified the PSMA peptide linker by substitution of a glutamic acid into a lysine residue, providing a handle for conjugation of multiple functional moieties. Ligand optimization showed that the new backbone structure leads to high-affinity PSMA ligands (all IC50 < 50 nM). Moreover, ligand-mediated PDT led to a PSMA-specific decrease in cell viability in vitro (P < 0.001). Linker modification significantly improved tumor targeting compared to the previously developed PSMA-N064 ligand (≥ 20 ± 3%ID/g vs 14 ± 2%ID/g, P < 0.01) and enabled specific visualization of PMSA-positive tumors using both radionuclide and fluorescence imaging in mice.

Conclusion: The new high-affinity dual-labeled PSMA-targeting ligands with optimized backbone compositions showed increased tumor targeting and enabled multimodal image-guided PCa surgery combined with targeted photodynamic therapy.

Keywords: Intraoperative; Multimodal imaging; PSMA; Photodynamic therapy; Prostate cancer.

MeSH terms

  • Animals
  • Antigens, Surface / metabolism
  • Cell Line, Tumor
  • Glutamate Carboxypeptidase II / metabolism
  • Humans
  • Ligands
  • Male
  • Mice
  • Mice, Nude
  • Multimodal Imaging
  • Photochemotherapy*
  • Photosensitizing Agents / therapeutic use
  • Precision Medicine
  • Prostatic Neoplasms* / drug therapy
  • Prostatic Neoplasms* / therapy
  • Tissue Distribution

Substances

  • Antigens, Surface
  • Ligands
  • Photosensitizing Agents
  • Glutamate Carboxypeptidase II