Department of Urology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Cancers (Basel). 2010 Jul 6;2(3):1432-40. doi: 10.3390/cancers2031432.
The search for the biomarkers to precisely and non-invasively characterize the biology of prostate cancer (PCa) is the focus of many laboratories across the world. Although prostate-specific antigen (PSA) remains the standard diagnostic tool for PCa, its low specificity leads to unnecessary biopsies in a substantial number of patients. More importantly, with the current status of knowledge, it is very difficult to early identify individuals with a life-threatening disease who require an immediate treatment. The significant advances in genetics and biotechnology in recent years has led to the discovery of new molecular markers including PCA3 and the TMPRSS2:ERG genomic fusion. Both PCA3 and TMPRSS2:ERG, compared to PSA, show an increased specificity in PCa detection. However, the quest for a single PCa marker that can fully satisfy urologists and their patients is still ongoing. The aim of this review is to present the recent findings on PCA3 and TMPRSS2:ERG and to describe their clinical implications and performance.
寻找能够精确、无创地描述前列腺癌(PCa)生物学特征的生物标志物是全球许多实验室的研究重点。尽管前列腺特异性抗原(PSA)仍然是 PCa 的标准诊断工具,但由于其特异性较低,导致大量患者进行了不必要的活检。更重要的是,根据目前的知识水平,很难早期识别出患有危及生命疾病、需要立即治疗的个体。近年来遗传学和生物技术的显著进步,导致发现了新的分子标志物,包括 PCA3 和 TMPRSS2:ERG 基因组融合。与 PSA 相比,PCA3 和 TMPRSS2:ERG 在 PCa 检测中的特异性都有所提高。然而,寻找一种能够完全满足泌尿科医生及其患者需求的单一 PCa 标志物的探索仍在继续。本文旨在介绍 PCA3 和 TMPRSS2:ERG 的最新发现,并描述它们的临床意义和性能。