McCabe N P, Angwafo F F, Zaher A, Selman S H, Kouinche A, Jankun J
Urology Research Center, Department of Urology, Medical College of Ohio, Toledo, OH 43614-2589, USA.
Oncol Rep. 2000 Jul-Aug;7(4):879-82. doi: 10.3892/or.7.4.879.
The urokinase-type plasminogen activator receptor (uPAR) exists as a GPI anchored glycoprotein (Mr=50-60 kDa) on the surface of various cell types. This receptor can be bound by or cleaved by urokinase. The cleaved receptor, soluble urokinase-type plasminogen activator receptor (suPAR), with an Mr=35 kDa has no known physiological function and can be identified circulating in the blood of normal individuals. Although no function has been characterized, the soluble receptor has been reported to be of clinical significance. The objective of this study is to characterize novel serum markers that can be used for the early detection of prostate cancer and to predict patient prognosis. Thirty-nine patients at the University of Yaounde I, Yaounde, Cameroon, West Africa were examined for prostatic disorders. Of these, 46% were diagnosed with benign prostate hyperplasia (BPH), while 44% of the patients were diagnosed via biopsy with prostate cancer and graded accordingly. Here we show that serum from patients with BPH or prostate cancer contains elevated levels of suPAR. To examine the significance of suPAR as a diagnostic factor, we used a suPAR ELISA kit and compared these results with serum levels of prostate specific antigen (PSA), the current diagnostic marker for prostate cancer. PSA and serum suPAR levels in BPH and cancer patients were greatly elevated in the majority of patients, while others had undetectable levels of either. Serum levels of suPAR were high in cancer patients as well as, although to a lesser degree, in patients with BPH. Cancer patients who died during the follow-up period were found to have consistently higher serum suPAR levels than correlating serum PSA levels. These preliminary findings are the first evaluating serum suPAR levels as a possible diagnostic marker for the early detection of prostate cancer and for the prediction of patient prognosis.
尿激酶型纤溶酶原激活物受体(uPAR)以糖基磷脂酰肌醇(GPI)锚定糖蛋白的形式(分子量为50 - 60 kDa)存在于多种细胞类型的表面。该受体可与尿激酶结合或被其切割。切割后的受体,即可溶性尿激酶型纤溶酶原激活物受体(suPAR),分子量为35 kDa,目前尚无已知的生理功能,且可在正常个体的血液中检测到。尽管其功能尚未明确,但据报道可溶性受体具有临床意义。本研究的目的是鉴定可用于早期检测前列腺癌并预测患者预后的新型血清标志物。在喀麦隆雅温得第一大学对39例患有前列腺疾病的患者进行了检查。其中,46%被诊断为良性前列腺增生(BPH),而44%的患者经活检诊断为前列腺癌并进行了分级。在此我们表明,BPH或前列腺癌患者的血清中suPAR水平升高。为了检验suPAR作为诊断因子的意义,我们使用了suPAR ELISA试剂盒,并将这些结果与前列腺癌目前的诊断标志物前列腺特异性抗原(PSA)的血清水平进行了比较。BPH和癌症患者中,大多数患者的PSA和血清suPAR水平大幅升高,而其他患者的这两种指标均检测不到。癌症患者以及BPH患者(程度较轻)的血清suPAR水平较高。在随访期间死亡的癌症患者,其血清suPAR水平始终高于相应的血清PSA水平。这些初步发现首次评估了血清suPAR水平作为早期检测前列腺癌和预测患者预后的可能诊断标志物。