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从成纤维细胞活化蛋白解码肿瘤:最新诊断与治疗前景综述

英文原题:Decoding tumors from fibroblast activation protein: A review of the latest diagnostic and therapeutic prospects.

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Decoding tumors from fibroblast activation protein: A review of the latest diagnostic and therapeutic prospects.

PubMed 2025/06/06(内容时间) Int J Biol Macromol Q1 · IF 8.7(JCR 2025)

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中文摘要

成纤维细胞活化蛋白(FAP)与肿瘤微环境(TME)密切相关,近年来受到广泛关注。FAP是一种II型跨膜丝氨酸蛋白酶,主要表达于癌症相关成纤维细胞(CAF),在肿瘤生长、侵袭、转移及免疫逃逸过程中发挥重要作用。超过90%的上皮癌中FAP高表达,因其灵敏度和特异性均较高,可作为理想的诊断标志物。使用放射性或荧光标记的FAP特异性分子探针,可实现高对比度肿瘤成像,从而辅助早期检测和监测。在治疗方面,靶向FAP的策略,包括FAP酶活性抑制剂、FAP特异性CAR-T 细胞和FAP疫苗,均显示出抑制肿瘤生长、降低肿瘤血管生成和增强抗肿瘤免疫的巨大潜力。为提高疗效并减少正常细胞损伤,这些策略还可与化疗、放疗和免疫治疗联合使用。本文综述FAP在肿瘤诊断和治疗方面的研究进展,并探讨其在肿瘤微环境中的关键作用及潜力。

展开英文摘要原文

Fibroblast activation protein (FAP), as a molecule closely associated with the tumor microenvironment (TME), has garnered widespread attention in recent years. FAP is a type II transmembrane serine protease primarily expressed in cancer-associated fibroblasts (CAFs), and it plays a significant role in tumor growth, invasion, metastasis, and immune evasion processes. FAP is highly expressed in over 90 % of epithelial cancers, which makes it a satisfactory diagnostic marker on account of its exceptional sensitivity and specificity. Using radio or fluorescence-labeled FAP-specific molecular probes can materialize high-contrast tumor imaging, and thereby facilitate early detection and monitoring.

With regard to treatment, FAP-targeting strategies like FAP enzyme activity inhibitors, FAP-specific Chimeric Antigen Receptor T-Cell (CAR-T) cells, and FAP vaccines have demonstrated tremendous potential to hinder tumor growth, lower tumor angiogenesis, and reinforce anti-tumor immunity.

For strengthening efficacy and lessening damage to normal cells, these strategies can also be integrated with chemotherapy, radiotherapy, and immunotherapy. This article not only reviews the research progress of FAP in tumor diagnosis and treatment, but also explores its paramount role and potential in the tumor microenvironment.

论文信息

作者
Wang Q、Song C、Zhao C、Wei X、Li D、Wu Q、Li J、Yang X
第一作者单位
School of Basic Medical Science, Guangxi Medical University, Nanning, Guangxi 530021, PR China.China
通讯作者单位
School of Basic Medical Science, Guangxi Medical University, Nanning, Guangxi 530021, PR China; Guangxi Key Laboratory of Nanobody Research, Guangxi Nanobody Engineering Research Center, Guangxi Medical University, Nanning, Guangxi 530021, PR China. Electronic address: yangxiaomei6009@sina.com.China
文献类型
综述
期刊
International journal of biological macromolecules2025 Jul
原文标识
PubMed 40484084 · DOI 10.1016/j.ijbiomac.2025.145006