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成纤维细胞激活蛋白抑制剂和肽的放射性分子治疗学。

Radiomolecular Theranostics With Fibroblast-Activation-Protein Inhibitors and Peptides.

机构信息

Curanosticum Wiesbaden-Frankfurt, Center for Advanced Radiomolecular Precision Oncology, Department of Nuclear Medicine, DKD HELIOS Klinik, Wiesbaden, Germany.

Department of Nuclear Medicine, Medical Faculty, Heinrich-Heine-University, University Hospital Düsseldorf, Düsseldorf, Germany.

出版信息

Semin Nucl Med. 2024 Jul;54(4):537-556. doi: 10.1053/j.semnuclmed.2024.05.010. Epub 2024 Jul 16.

Abstract

The advancement of theranostics, which combines therapeutic and diagnostic capabilities in oncology, has significantly impacted cancer management. This review explores fibroblast activation protein (FAP) expression in the tumor microenvironment (TME) and its association with various malignancies, highlighting its potential as a theranostic marker for PET/CT imaging using FAP-targeted tracers and for FAP-targeted radiopharmaceutical therapy. We examine the development and clinical applications of FAP inhibitors (FAPIs) and peptides, providing insights into their diagnostic accuracy, initial therapeutic efficacy, and clinical impact across diverse cancer types, as well as the synthesis of novel FAP-targeted ligands. This review aims to showcase the promising outcomes and challenges in integrating FAP-targeted approaches into cancer management.

摘要

治疗诊断学的进步,将治疗和诊断能力结合在肿瘤学中,对癌症管理产生了重大影响。本综述探讨了成纤维细胞激活蛋白(FAP)在肿瘤微环境(TME)中的表达及其与各种恶性肿瘤的关联,强调了其作为使用 FAP 靶向示踪剂的 PET/CT 成像和 FAP 靶向放射性药物治疗的治疗诊断标志物的潜力。我们研究了 FAP 抑制剂(FAPIs)和肽的开发和临床应用,深入了解它们在不同癌症类型中的诊断准确性、初始治疗效果和临床影响,以及新型 FAP 靶向配体的合成。本综述旨在展示将 FAP 靶向方法整合到癌症管理中的有希望的结果和挑战。

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