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靶向成纤维细胞活化蛋白α的基于蛋白质的放射性药物:当前进展综述

Protein-based Radiopharmaceuticals that target fibroblast activation protein alpha: a review of current progress.

作者信息

Homedan Abdelrahman, Pandya Darpan N, Schnicker Nicholas J, Wadas Thaddeus J

机构信息

Department of Radiology, University of Iowa, Iowa City, IA, 52242, USA.

Protein and Crystallography Facility, University of Iowa, Iowa City, 52242, USA.

出版信息

EJNMMI Radiopharm Chem. 2025 Jun 21;10(1):32. doi: 10.1186/s41181-025-00356-5.


DOI:10.1186/s41181-025-00356-5
PMID:40542914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12182545/
Abstract

BACKGROUND: Fibroblast activation protein alpha (FAP) is a serine protease that is expressed at basal levels in benign tissues but is overexpressed in a variety of pathologies, including cancer. Consequently, significant research efforts have been expended to develop diagnostic radiopharmaceuticals and effective radiotherapies that target this protein. The aim of this review is to summarize the current progress on the development of protein-based radiopharmaceuticals that target FAP. MAIN BODY: A literature survey spanning nearly 40 years was conducted to assess the historical development and current progress in protein-based radiopharmaceuticals that target FAP. To date, more than 20 publications have been introduced that describe these agents in preclinical and clinical settings. This review summarizes the development and evaluation of radiopharmaceuticals involving antibodies, antibody fragments, and single domain antibodies. CONCLUSION: The results of this literature review demonstrate that while significant research efforts have been expended on peptide-based radiopharmaceuticals and small molecule FAP inhibitors, the development of protein-based radiopharmaceuticals that target FAP remains an active research area that has yet to reach its full potential.

摘要

背景:成纤维细胞活化蛋白α(FAP)是一种丝氨酸蛋白酶,在良性组织中呈基础水平表达,但在包括癌症在内的多种病理状态下过度表达。因此,人们投入了大量研究精力来开发针对该蛋白的诊断性放射性药物和有效的放射疗法。本综述的目的是总结靶向FAP的基于蛋白质的放射性药物的当前进展。 主体:进行了一项跨越近40年的文献调查,以评估靶向FAP的基于蛋白质的放射性药物的历史发展和当前进展。迄今为止,已有20多篇出版物介绍了这些药物在临床前和临床环境中的情况。本综述总结了涉及抗体、抗体片段和单域抗体的放射性药物的开发和评估。 结论:本综述结果表明,虽然在基于肽的放射性药物和小分子FAP抑制剂方面已经投入了大量研究精力,但靶向FAP的基于蛋白质的放射性药物的开发仍然是一个活跃的研究领域,尚未充分发挥其潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/0d508909ac1c/41181_2025_356_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/6591df8c7784/41181_2025_356_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/3537ae83e1e9/41181_2025_356_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/8a7f41ca53ec/41181_2025_356_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/fd8c6da68eab/41181_2025_356_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/3688b7da0e27/41181_2025_356_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/7290ef06d9bb/41181_2025_356_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/0d508909ac1c/41181_2025_356_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/6591df8c7784/41181_2025_356_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/3537ae83e1e9/41181_2025_356_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/8a7f41ca53ec/41181_2025_356_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/fd8c6da68eab/41181_2025_356_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/3688b7da0e27/41181_2025_356_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/7290ef06d9bb/41181_2025_356_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23f/12182545/0d508909ac1c/41181_2025_356_Fig7_HTML.jpg

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本文引用的文献

[1]
An iridium(iii) 3-chloro-6-thio-1,2,4,5-tetrazine complex for cysteine conjugation, bioimaging and photoactivated therapy.

RSC Chem Biol. 2025-5-7

[2]
Benign non-immune cells in tumor microenvironment.

Front Immunol. 2025-4-3

[3]
Breast Cancer and Tumor Microenvironment: The Crucial Role of Immune Cells.

Curr Oncol. 2025-2-28

[4]
New insights on anti-tumor immunity of CD8 T cells: cancer stem cells, tumor immune microenvironment and immunotherapy.

J Transl Med. 2025-3-17

[5]
FAP inhibitors: are we really using the best method to evaluate the residence time?

Eur J Nucl Med Mol Imaging. 2025-2-26

[6]
Cryo-electron microscopy reveals a single domain antibody with a unique binding epitope on fibroblast activation protein alpha.

RSC Chem Biol. 2025-2-6

[7]
Unique mechanisms to increase structural stability and enhance antigen binding in nanobodies.

Structure. 2025-4-3

[8]
Trends in nanobody technology in industrialization.

Discov Nano. 2025-2-10

[9]
High prevalence of FAP+ cancer-associated fibroblasts predicts poor outcome in patients with high-grade serous ovarian cancer with high CD8 T-cell density.

Gynecol Oncol. 2025-2

[10]
Strategies for specific multimodal imaging of cancer-associated fibroblasts and applications in theranostics of cancer.

Mater Today Bio. 2024-12-24

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