Homedan Abdelrahman, Pandya Darpan N, Schnicker Nicholas J, Wadas Thaddeus J
Department of Radiology, University of Iowa, Iowa City, IA, 52242, USA.
Protein and Crystallography Facility, University of Iowa, Iowa City, 52242, USA.
EJNMMI Radiopharm Chem. 2025 Jun 21;10(1):32. doi: 10.1186/s41181-025-00356-5.
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.
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。
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