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前列腺癌中前列腺特异性膜抗原(PSMA)表达、调控及异质性的生物学决定因素

Biological determinants of PSMA expression, regulation and heterogeneity in prostate cancer.

作者信息

Bakht Martin K, Beltran Himisha

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

Harvard Medical School, Boston, MA, USA.

出版信息

Nat Rev Urol. 2025 Jan;22(1):26-45. doi: 10.1038/s41585-024-00900-z. Epub 2024 Jul 8.

Abstract

Prostate-specific membrane antigen (PSMA) is an important cell-surface imaging biomarker and therapeutic target in prostate cancer. The PSMA-targeted theranostic Lu-PSMA-617 was approved in 2022 for men with PSMA-PET-positive metastatic castration-resistant prostate cancer. However, not all patients respond to PSMA-radioligand therapy, in part owing to the heterogeneity of PSMA expression in the tumour. The PSMA regulatory network is composed of a PSMA transcription complex, an upstream enhancer that loops to the FOLH1 (PSMA) gene promoter, intergenic enhancers and differentially methylated regions. Our understanding of the PSMA regulatory network and the mechanisms underlying PSMA suppression is evolving. Clinically, molecular imaging provides a unique window into PSMA dynamics that occur on therapy and with disease progression, although challenges arise owing to the limited resolution of PET. PSMA regulation and heterogeneity - including intertumoural and inter-patient heterogeneity, temporal changes, lineage dynamics and the tumour microenvironment - affect PSMA theranostics. PSMA response and resistance to radioligand therapy are mediated by a number of potential mechanisms, and complementary biomarkers beyond PSMA are under development. Understanding the biological determinants of cell surface target regulation and heterogeneity can inform precision medicine approaches to PSMA theranostics as well as other emerging therapies.

摘要

前列腺特异性膜抗原(PSMA)是前列腺癌中一种重要的细胞表面成像生物标志物和治疗靶点。靶向PSMA的治疗诊断药物Lu-PSMA-617于2022年获批用于PSMA-PET阳性的转移性去势抵抗性前列腺癌男性患者。然而,并非所有患者都对PSMA放射性配体疗法有反应,部分原因是肿瘤中PSMA表达的异质性。PSMA调控网络由一个PSMA转录复合体、一个与FOLH1(PSMA)基因启动子环化的上游增强子、基因间增强子和差异甲基化区域组成。我们对PSMA调控网络以及PSMA抑制背后机制的理解正在不断发展。临床上,分子成像为治疗过程中和疾病进展过程中发生的PSMA动态变化提供了一个独特的窗口,尽管由于PET分辨率有限会出现一些挑战。PSMA的调控和异质性——包括肿瘤间和患者间的异质性、时间变化、谱系动态以及肿瘤微环境——会影响PSMA治疗诊断。PSMA对放射性配体疗法的反应和耐药性是由多种潜在机制介导的,除PSMA之外的互补生物标志物也正在研发中。了解细胞表面靶点调控和异质性的生物学决定因素可为PSMA治疗诊断以及其他新兴疗法的精准医学方法提供依据。

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