Stephan Carsten, Jung Klaus, Lein Michael, Diamandis Eleftherios P
Department of Urology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Eur J Cancer. 2007 Sep;43(13):1918-26. doi: 10.1016/j.ejca.2007.06.006. Epub 2007 Aug 3.
Prostate cancer is the most common neoplasia of middle-aged men. Prostate specific antigen (PSA) is the first FDA-approved tumour marker for early detection of cancer and it is now in widespread clinical use. The discovery of different PSA molecular forms in serum (free PSA, PSA complexed with various protease inhibitors) in the early 1990s renewed clinical research to enhance the specificity of PSA. Also, the use of a homologous prostate-localised antigen, human glandular kallikrein 2 (KLK2) may further reduce the number of unnecessary prostate biopsies. More recently, promising data is emerging regarding molecular forms of free PSA (proPSA, BPSA, 'intact' PSA) and other members of the expanded human kallikrein family. These new findings may add substantial clinical information for early detection of prostate cancer.
前列腺癌是中年男性最常见的肿瘤。前列腺特异性抗原(PSA)是首个获美国食品药品监督管理局(FDA)批准用于癌症早期检测的肿瘤标志物,目前已在临床广泛应用。20世纪90年代初血清中不同PSA分子形式(游离PSA、与各种蛋白酶抑制剂结合的PSA)的发现,重新激发了旨在提高PSA特异性的临床研究。此外,使用同源的前列腺定位抗原——人腺体激肽释放酶2(KLK2),可能会进一步减少不必要的前列腺活检数量。最近,关于游离PSA的分子形式(proPSA、BPSA、“完整”PSA)以及扩展的人激肽释放酶家族的其他成员,出现了一些有前景的数据。这些新发现可能会为前列腺癌的早期检测增添大量临床信息。