Beyond Small Molecules: Antibodies and Peptides for Fibroblast Activation Protein Targeting Radiopharmaceuticals

被引:5
|
作者
Sun, Xiaona [1 ,2 ]
Wu, Yuxuan [1 ,2 ]
Wang, Xingkai [2 ]
Gao, Xin [2 ]
Zhang, Siqi [2 ]
Sun, Zhicheng [1 ]
Liu, Ruping [1 ]
Hu, Kuan [2 ]
机构
[1] Beijing Inst Graph Commun, Sch Printing & Packaging Engineer, Beijing 102600, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing 100050, Peoples R China
关键词
FAP; radiopharmaceuticals; PET imaging; theranostics; radionuclide therapy; CANCER-ASSOCIATED FIBROBLASTS; CARCINOMA-ASSOCIATED FIBROBLASTS; INHIBIT TUMOR-GROWTH; MONOCLONAL-ANTIBODY; STROMAL FIBROBLASTS; SERINE-PROTEASE; DIFFERENTIAL EXPRESSION; DIPEPTIDYL-PEPTIDASE; STELLATE CELLS; LUNG-CANCER;
D O I
10.3390/pharmaceutics16030345
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fibroblast activation protein (FAP) is a serine protease characterized by its high expression in cancer-associated fibroblasts (CAFs) and near absence in adult normal tissues and benign lesions. This unique expression pattern positions FAP as a prospective biomarker for targeted tumor radiodiagnosis and therapy. The advent of FAP-based radiotheranostics is anticipated to revolutionize cancer management. Among various types of FAP ligands, peptides and antibodies have shown advantages over small molecules, exemplifying prolonged tumor retention in human volunteers. Within its scope, this review summarizes the recent research progress of the FAP radiopharmaceuticals based on antibodies and peptides in tumor imaging and therapy. Additionally, it incorporates insights from recent studies, providing valuable perspectives on the clinical utility of FAP-targeted radiopharmaceuticals.
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页数:24
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