Preclinical Evaluation of <sup>68</sup> Ga-Labeled CSPG4-Targeting Peptides for PET/CT Imaging in Pancreatic and Gastric Carcinoma

Chondroitin sulfate proteoglycan 4 (CSPG4) is highly expressed in various solid tumors and promotes tumor progression and migration. Targeting CSPG4 therapy, such as monoclonal antibodies 9.2.27 and CAR-M, has already been in clinical trials. Database analysis further correlated elevated levels of CSPG4 with reduced overall survival in both cancers. Achieving real-time visualization of aberrant CSPG4 expression in various solid tumors remains a critical issue that needs to be addressed. To address this, we pioneered the preparation of three <sup>68</sup>Ga-labeled PET probes targeting CSPG4, [<sup>68</sup>Ga]Ga-DOTA-LS10, [<sup>68</sup>Ga]Ga-DOTA-SH11, and [<sup>68</sup>Ga]Ga-DOTA-TH10. In pancreatic (ASPC1) and gastric (MKN45) carcinoma models, [<sup>68</sup>Ga]Ga-DOTA-TH10 showed prominent tumor uptake (ASPC1:1.63 ± 0.15%ID/g at 60 min), validated by Western blot and immunohistochemistry confirming CSPG4 overexpression. This study conducted the first PET imaging on CSPG4 expression in pancreatic cancer and gastric cancer models using <sup>68</sup>Ga-labeled peptides, aiming to provide guidance for clinical real-time monitoring of its expression.

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Journal
Journal of Medicinal Chemistry
Published
2025-10-15
DOI
https://doi.org/10.1021/acs.jmedchem.5c02187
Primary Topic
Peptidase Inhibition and Analysis
Type
article
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article

Preclinical Evaluation of 68 Ga-Labeled CSPG4-Targeting Peptides for PET/CT Imaging in Pancreatic and Gastric Carcinoma

Fengsheng Zhang, Jindian Li, Ye Li, Zerong Wang et al.
Journal of Medicinal Chemistry
Peptidase Inhibition and Analysis
article

Preclinical Evaluation of 68 Ga-Labeled CSPG4-Targeting Peptides for PET/CT Imaging in Pancreatic and Gastric Carcinoma

Fengsheng Zhang, Jindian Li, Ye Li, Zerong Wang, Xiaoyu Pan, Linjie Bian
article en

Abstract

Chondroitin sulfate proteoglycan 4 (CSPG4) is highly expressed in various solid tumors and promotes tumor progression and migration. Targeting CSPG4 therapy, such as monoclonal antibodies 9.2.27 and CAR-M, has already been in clinical trials. Database analysis further correlated elevated levels of CSPG4 with reduced overall survival in both cancers. Achieving real-time visualization of aberrant CSPG4 expression in various solid tumors remains a critical issue that needs to be addressed. To address this, we pioneered the preparation of three <sup>68</sup>Ga-labeled PET probes targeting CSPG4, [<sup>68</sup>Ga]Ga-DOTA-LS10, [<sup>68</sup>Ga]Ga-DOTA-SH11, and [<sup>68</sup>Ga]Ga-DOTA-TH10. In pancreatic (ASPC1) and gastric (MKN45) carcinoma models, [<sup>68</sup>Ga]Ga-DOTA-TH10 showed prominent tumor uptake (ASPC1:1.63 ± 0.15%ID/g at 60 min), validated by Western blot and immunohistochemistry confirming CSPG4 overexpression. This study conducted the first PET imaging on CSPG4 expression in pancreatic cancer and gastric cancer models using <sup>68</sup>Ga-labeled peptides, aiming to provide guidance for clinical real-time monitoring of its expression.

Journal of Medicinal ChemistryVol. 68(21)
Shanghai Medical College of Fudan University (CN), Fudan University (CN), Fudan University Shanghai Cancer Center (CN), Institute of Modern Physics (CN)
Openalex Percentile: Top 61%
Peptidase Inhibition and Analysis
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