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MR Molecular Imaging of Prostate Cancer with a Small Molecular CLT1 Peptide Targeted Contrast Agent
Published on: September 3, 2013
Biphenyl-Trimeric PSMA Theranostic Platform Enables PET Imaging and Optical Detection of Prostate Cancer
Yimin Chen1, Haonan Yu2, Wanjia Liu1
1Key Laboratory of Radiopharmaceuticals, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing 100875, China.
None:
Prostate cancer (PCa) diagnosis faces challenges with current imaging tracers in sensitivity and contrast. We developed a biphenyl-trimeric PSMA-targeted theranostic system to address these challenges. A suite of trimeric PSMA probes (PSMA-T0-T6) was synthesized using a biphenyl scaffold and variable linkers, showing exceptional PSMA affinity (Ki = 0.11-0.60 nM). Preclinical studies demonstrated that [68Ga]Ga-PSMA-T3 provided superior tumor uptake (SUVmax 1.16 vs 0.61) and tumor-to-background ratios (TBR 26.82 vs 19.89) over [68Ga]Ga-PSMA-11 in 22Rv1 tumor-bearing mice. The optical counterpart, ICG-conjugated PSMA-T6, prolonged tumor retention with high tumor-to-muscle ratio (T/M = 7.3 at 24 h) and remarkable ex vivo specificity (T/M = 41.9). In first-in-human PET studies, [68Ga]Ga-PSMA-T3 showed comparable and enhanced detection rates of primary and metastatic lesions, particularly in liver and bone metastases, with higher TBR values than [68Ga]Ga-PSMA-11. Our biphenyl-trimeric PSMA platform demonstrates translational potential for enhanced diagnostic sensitivity and intraoperative management of PCa.
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