Design and Preclinical Evaluation of First <sup>68</sup> Ga-Labeled Cathepsin D-Targeted Radiotracers

Cathepsin D (CTSD), a lysosomal aspartic protease linked to cancer progression and poor patient outcomes, is underexplored as a diagnostic biomarker. This study developed the first CTSD-targeted radiotracers, identifying [<sup>68</sup>Ga]Ga-NOTA-FZCD-3 as optimal due to its strong binding to CTSD (dissociation constant = 0.65 μM), rapid clearance from the body (elimination half-life = 16.61 min), and high tumor-specific uptake in mouse models. Imaging analysis revealed that tumors with higher CTSD levels absorbed more of the tracer, particularly in the MDA-MB-175VII model, which showed the highest tumor uptake (3.63 ± 0.32%ID/g at 0.5 h) and excellent tumor/nontumor contrast (7.65 ± 1.14 at 1 h). The tracer remained stable in blood for over 2 h without causing toxicity. These findings highlight CTSD as a key cancer biomarker and demonstrate the potential of this radiotracer for improving early cancer detection and monitoring therapy response in patients.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-11-26
DOI
https://doi.org/10.1021/acs.jmedchem.5c02151
Primary Topic
Protease and Inhibitor Mechanisms
Type
article
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article

Design and Preclinical Evaluation of First 68 Ga-Labeled Cathepsin D-Targeted Radiotracers

Xiangwei Wang, Mengjing Ji, Simin He, Shaoli Song et al.
Journal of Medicinal Chemistry
Protease and Inhibitor Mechanisms
article

Design and Preclinical Evaluation of First 68 Ga-Labeled Cathepsin D-Targeted Radiotracers

Xiangwei Wang, Mengjing Ji, Simin He, Shaoli Song, Jianping Zhang, Xiaoping Xu, Yue Xi
article en

Abstract

Cathepsin D (CTSD), a lysosomal aspartic protease linked to cancer progression and poor patient outcomes, is underexplored as a diagnostic biomarker. This study developed the first CTSD-targeted radiotracers, identifying [<sup>68</sup>Ga]Ga-NOTA-FZCD-3 as optimal due to its strong binding to CTSD (dissociation constant = 0.65 μM), rapid clearance from the body (elimination half-life = 16.61 min), and high tumor-specific uptake in mouse models. Imaging analysis revealed that tumors with higher CTSD levels absorbed more of the tracer, particularly in the MDA-MB-175VII model, which showed the highest tumor uptake (3.63 ± 0.32%ID/g at 0.5 h) and excellent tumor/nontumor contrast (7.65 ± 1.14 at 1 h). The tracer remained stable in blood for over 2 h without causing toxicity. These findings highlight CTSD as a key cancer biomarker and demonstrate the potential of this radiotracer for improving early cancer detection and monitoring therapy response in patients.

Journal of Medicinal ChemistryVol. 68(23)
Shanghai Medical College of Fudan University (CN), Fudan University (CN), Fudan University Shanghai Cancer Center (CN), Tracer Technologies (United States) (US), Laboratoire d’Imagerie Biomédicale (FR), United Imaging Healthcare (China) (CN)
Openalex Percentile: Top 55%
Protease and Inhibitor Mechanisms
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