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前列腺癌细胞表面蛋白靶向治疗进展(综述)

英文原题:Progress in targeted therapy for prostate cancer via cell surface proteins (Review).

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Progress in targeted therapy for prostate cancer via cell surface proteins (Review).

PubMed 2025/11/05(内容时间) Biomed Rep Q3 · IF 2.5(JCR 2025)

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中文摘要

前列腺癌(PCa),尤其是转移性去势抵抗性PCa,仍然是一个重大的治疗挑战。细胞表面蛋白已成为有前景的治疗靶点。本综述探讨了PCa细胞表面蛋白的生物学特征,重点关注主要靶点,如前列腺特异性膜抗原、六跨膜上皮抗原1、滋养层细胞表面抗原2和前列腺干细胞抗原。这些靶点为新兴治疗策略的开发提供了基础,包括放射性配体治疗、抗体-药物偶联物以及双特异性T细胞和CAR-T 细胞治疗。结合最新临床试验数据,本综述讨论了靶向治疗的疗效、药物治疗耐药机制和联合治疗策略,分析了它们在PCa管理中的潜在应用,并探讨了未来精准治疗发展的前景。此外,本综述旨在系统总结该领域的相关进展。总之,这些发现为PCa的分子靶向治疗提供了理论基础和临床指导,从而促进进一步的研究和应用。

展开英文摘要原文

Prostate cancer (PCa), particularly metastatic castration-resistant PCa, remains a significant therapeutic challenge. Cell-surface proteins have emerged as promising therapeutic targets. The present review examines the biological characteristics of PCa cell surface proteins focusing on major targets, such as prostate-specific membrane antigen, six-transmembrane epithelial antigen 1, trophoblast cell-surface antigen 2, and prostate stem cell antigen.

These targets provide the foundation for the development of emerging therapeutic strategies, including radioligand therapy, antibody-drug conjugates, and bispecific T cells and chimeric antigen receptor T cell therapy. Combining the latest clinical trial data, the present review discusses the efficacy of targeted therapy, the mechanisms of drug therapy resistance, and combination treatment strategies, analyzing their potential application in the management of PCa and exploring prospects for the development of precision therapy in the future.

Additionally, this review aims to systematically summarize the relevant progress in this field.

In conclusion, the findings provide a theoretical basis and clinical guidance for molecular-targeted therapy in PCa, thereby promoting further research and applications.

论文信息

作者
Luo H
单位
Department of Urology, Deyang Hospital of Sichuan Provincial People's Hospital, Deyang, Sichuan 618000, P.R. China.China
文献类型
综述
期刊
Biomedical reports2026 Jan
原文标识
PubMed 41282505 · DOI 10.3892/br.2025.2080