Casella Roberto, Shariat Shahrokh F, Monoski Mara A, Lerner Seth P
The Scott Department of Urology, Baylor College of Medicine and The Methodist Hospital, Houston, Texas 77030, USA.
Cancer. 2002 Dec 15;95(12):2494-9. doi: 10.1002/cncr.10989.
The authors found previously that plasma levels of urokinase-type plasminogen activator (uPA) and its receptor (uPAR) were elevated in patients with bladder carcinoma and were associated with features of biologically aggressive disease. In the current study, they tested the hypothesis that elevated urinary levels of uPA and uPAR would predict the presence of bladder malignancy by comparing the performance of uPA and uPAR with the performance of bladder wash-out cytology in the noninvasive diagnosis of bladder tumors.
An enzyme-linked immunosorbent assay was used to compare levels of uPA and uPAR in urine that was collected before cystoscopy from 122 patients with bladder carcinoma and from 107 participants in a control group. Seventy-two patients had clinical Tis or Ta transitional cell carcinoma, and 50 patients had invasive disease (>or= T1); 85 patients had clinical Grade 1-2 tumors, and 37 patients had Grade 3 tumors. For cytology, only high grade was considered positive.
Urinary levels of uPA and uPAR were higher in patients with bladder carcinoma compared with levels in the control group (P < 0.001 and P = 0.016, respectively). However, only uPA levels were elevated in patients with abnormal urinary cytology (P = 0.006). After controlling for cytology (odds ratio [OR], 10.182; 95% confidence interval [95%CI], 4.451-23.291; P < 0.001), uPAR (P for trend = 0.168), and age (P = 0.091), those in the highest quartile for uPA had an increased risk of bladder carcinoma compared with those in the lowest quartile (OR, 3.022; 95%CI, 1.295-7.054; P for trend = 0.031).
The current findings suggest that urinary levels of uPA, but not uPAR, are related to the risk of bladder carcinoma. The study confirmed the central role of urinary cytology in the noninvasive diagnosis of bladder carcinoma.
作者之前发现,尿激酶型纤溶酶原激活剂(uPA)及其受体(uPAR)的血浆水平在膀胱癌患者中升高,且与具有生物学侵袭性疾病的特征相关。在当前研究中,他们通过比较uPA和uPAR与膀胱冲洗细胞学在膀胱肿瘤非侵入性诊断中的表现,来检验尿中uPA和uPAR水平升高可预测膀胱恶性肿瘤存在这一假设。
采用酶联免疫吸附测定法,比较122例膀胱癌患者和107例对照组参与者在膀胱镜检查前收集的尿液中uPA和uPAR的水平。72例患者患有临床Tis或Ta期移行细胞癌,50例患者患有浸润性疾病(≥T1期);85例患者患有临床1 - 2级肿瘤,37例患者患有3级肿瘤。对于细胞学检查,仅高级别被视为阳性。
与对照组相比,膀胱癌患者尿液中uPA和uPAR的水平更高(分别为P < 0.001和P = 0.016)。然而,尿液细胞学异常的患者中仅uPA水平升高(P = 0.006)。在控制了细胞学(比值比[OR],10.182;95%置信区间[95%CI],4.451 - 23.291;P < 0.00i)、uPAR(趋势P = 0.168)和年龄(P = 0.091)后,uPA处于最高四分位数的患者与处于最低四分位数的患者相比,患膀胱癌的风险增加(OR,3.022;95%CI,1.295 - 7.054;趋势P = 0.031)。
当前研究结果表明,尿液中uPA水平而非uPAR水平与膀胱癌风险相关。该研究证实了尿液细胞学在膀胱癌非侵入性诊断中的核心作用。