Design and Preclinical Evaluation of a Novel Prostate-Specific Membrane Antigen Radioligand Modified with a Transthyretin Binder.
Christian VaccarinAna Katrina MapanaoLuisa M DeberleAnna E BeckerFrancesca BorgnaGiovanni MarzaroRoger SchibliCristina MüllerPublished in: Cancers (2024)
Transthyretin binders have previously been used to improve the pharmacokinetic properties of small-molecule drug conjugates and could, thus, be utilized for radiopharmaceuticals as an alternative to the widely explored "albumin binder concept". In this study, a novel PSMA ligand modified with a transthyretin-binding entity (TB-01) was synthesized and labeled with lutetium-177 to obtain [ 177 Lu]Lu-PSMA-TB-01. A high and specific uptake of [ 177 Lu]Lu-PSMA-TB-01 was found in PSMA-positive PC-3 PIP cells (69 ± 3% after 4 h incubation), while uptake in PSMA-negative PC-3 flu cells was negligible (<1%). In vitro binding studies showed a 174-fold stronger affinity of [ 177 Lu]Lu-PSMA-TB-01 to transthyretin than to human serum albumin. Biodistribution studies in PC-3 PIP/flu tumor-bearing mice confirmed the enhanced blood retention of [ 177 Lu]Lu-PSMA-TB-01 (16 ± 1% IA/g at 1 h p.i.), which translated to a high tumor uptake (69 ± 13% IA/g at 4 h p.i.) with only slow wash-out over time (31 ± 8% IA/g at 96 h p.i.), while accumulation in the PC-3 flu tumor and non-targeted normal tissue was reasonably low. Further optimization of the radioligand design would be necessary to fine-tune the biodistribution and enable its use for therapeutic purposes. This study was the first of this kind and could motivate the use of the "transthyretin binder concept" for the development of future radiopharmaceuticals.
Keyphrases
- pet imaging
- pet ct
- mycobacterium tuberculosis
- small molecule
- wild type
- induced apoptosis
- positron emission tomography
- prostate cancer
- cell cycle arrest
- stem cells
- emergency department
- computed tomography
- oxidative stress
- dna binding
- endoplasmic reticulum stress
- cell therapy
- binding protein
- cell death
- mesenchymal stem cells
- cell proliferation
- insulin resistance
- pi k akt