Expression of UPA and UPAR is associated with the clinical course of urinary bladder neoplasms

被引:29
作者
Seddighzadeh, M
Steineck, G
Larsson, P
Wijkström, H
Norming, U
Onelöv, E
Linder, S
机构
[1] Karolinska Inst & Hosp, Can Ctr Karolinska, S-17176 Stockholm, Sweden
[2] Karolinska Hosp & Inst, Dept Oncol Pathol, Stockholm, Sweden
[3] Huddinge Univ Hosp, Dept Urol, S-14186 Huddinge, Sweden
[4] Stockholm S Hosp, Dept Urol, Stockholm, Sweden
关键词
bladder cancer; urokinase; urokinase receptor; mRNA expression; survival; metastasis;
D O I
10.1002/ijc.10426
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The expression of urokinase plasminogen activator (uPA) and its receptor (uPAR) nRNA was determined in 194 subjects with newly detected bladder neoplasms, selected from a larger population-based series. An association was found between uPA and uPAR expression (n = 172; Spearman r(s) = 0.60, p < 0.001). Both uPA and uPAR mRNA levels were higher in muscle invasive (T2+) tumors than in noninvasive mucosal tumors (Ta) or those invading submucosa (T 1). The relative hazard ratios (RHRs) for cancer-specific death associated with elevated expression (95% CI), adjusted for age and gender in a Cox proportional hazard model, were 1.8 (1.0-3.3) for uPA (upper quartile cut-line), 2.2 (1.3-4.0) for uPAR (median quartile cut-line) and 2.5 (1.3-4.9) for uPA + uPAR. An RHR for metastatic disease of 4.0 (1.6-9.9) was observed for uPAR. Restricting the analyses to T2+ tumors, the corresponding figures were: 2.1 (1.1-3.9) for uPA, 1.6 (0.8-3.3) for uPAR and 2.5 (1.1-5.6) for both. We conclude that expression of uPA and uPAR is associated with the clinical behaviour of bladder neoplasms, possibly providing means for refined staging of muscle invasive tumors and target proteins for novel therapies. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:721 / 726
页数:6
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