Predictive Value of the Differential Expression of the Urokinase Plasminogen Activation Axis in Radical Prostatectomy Patients

被引:50
作者
Gupta, Amit [1 ]
Lotan, Yair [1 ]
Ashfaq, Raheela [2 ]
Roehrborn, Claus G. [1 ]
Raj, Ganesh V. [1 ]
Aragaki, Corinne C. [3 ]
Montorsi, Francesco [4 ]
Shariat, Shahrokh F. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Urol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[3] Univ Texas MD Anderson Canc Ctr, Univ Texas Sch Publ Hlth, Ctr Human Genet, Houston, TX 77030 USA
[4] Univ Vita Salute San Raffaele, Sci Inst H San Raffaele, Dept Urol, Milan, Italy
关键词
Biochemical failure; Prostatic neoplasms; Recurrence; Radical Prostatectomy; Urokinase plasminogen activator; BREAST-CANCER PATIENTS; POTENTIAL MARKER; CELL CARCINOMA; TUMOR-GROWTH; RETROPUBIC PROSTATECTOMY; ADJUVANT CHEMOTHERAPY; SYNTHETIC INHIBITOR; COLORECTAL-CANCER; HIGH-RISK; IN-VIVO;
D O I
10.1016/j.eururo.2008.06.054
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: The urokinase plasminogen axis is composed of urokinase plasminogen activator (uPA), its receptor (uPAR), and its inhibitors (PAI-1 and PAI-2). This axis is involved in cell proliferation, angiogenesis, extracellular matrix degradation, invasion, and metastases. Objective: To assess the relationship of the uPA axis with pathologic features and outcomes in prostate cancer. Interventions: None. Measurements: Immunohistochemical staining for uPA, uPAR, and PAI-1 were carried out on serial archival tissue microarray specimens. These markers were histologically categorized as normal or overexpressed. Disease recurrence was classified as aggressive if metastases were present, if postrecurrence prostate-specific antigen (PSA) doubling time was <10 mo, or if the patients failed to respond to salvage local radiation therapy. Results and limitations: The median follow-up was 63 mo. The combined expression of uPA and PAI-1 was associated with extraprostatic extension (p = 0.01) and seminal vesicle invasion (p = 0.008). On multivariable analysis, the combined uPA/PAI-1 expression was associated with overall (risk ratio [RR]: 2.3; 95% confidence interval [CI]: 1.1-4.8; p = 0.02) and aggressive disease recurrence (RR: 9.4; 95% Cl: 3.5-25; p < 0.0001) but not with nonaggressive disease recurrence. Expression of uPAR was not associated with any of the outcomes. The study is limited by its retrospective nature and lack of long-term follow-up. Conclusions: Overexpression of both uPA and PAI-1 is associated with adverse pathologic features and higher risk of overall and aggressive disease recurrence in men treated with radical prostatectomy for clinically localized prostate cancer. After validation, these markers may be useful in selecting patients most likely to benefit from adjuvant therapy. These markers should also be considered for addition into postoperative prediction tools. (C) 2008 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1124 / 1133
页数:10
相关论文
共 39 条
[1]  
ACHBAROU A, 1994, CANCER RES, V54, P2372
[2]   Å6, a urokinase plasminogen activator (uPA)-derived peptide in patients with advanced gynecologic cancer:: A phase I trial [J].
Berkenblit, A ;
Matulonis, UA ;
Kroener, JF ;
Dezube, BJ ;
Lam, GN ;
Cuasay, LC ;
Brünner, N ;
Jones, TR ;
Silverman, MH ;
Gold, MA .
GYNECOLOGIC ONCOLOGY, 2005, 99 (01) :50-57
[3]   Evaluation of urokinase plasminogen activator and its receptor in different grades of human prostate cancer [J].
Cozzi, Paul J. ;
Wang, Jian ;
Delprado, Warick ;
Madigan, Michele C. ;
Fairy, Stephen ;
Russell, Pamela J. ;
Li, Yong .
HUMAN PATHOLOGY, 2006, 37 (11) :1442-1451
[4]   PREVENTION OF METASTASIS BY INHIBITION OF THE UROKINASE RECEPTOR [J].
CROWLEY, CW ;
COHEN, RL ;
LUCAS, BK ;
LIU, GH ;
SHUMAN, MA ;
LEVINSON, AD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :5021-5025
[5]  
Dondi D, 2006, ONCOL REP, V15, P393
[6]   The urokinase plasminogen activator system: Role in malignancy [J].
Duffy, MJ .
CURRENT PHARMACEUTICAL DESIGN, 2004, 10 (01) :39-49
[7]   Inhibition of the invasion capacity of carcinoma cells by WX-UK1, a novel synthetic inhibitor of the urokinase-type plasminogen activator system [J].
Ertongur, S ;
Lang, S ;
Mack, B ;
Wosikowski, K ;
Muehlenweg, B ;
Gires, O .
INTERNATIONAL JOURNAL OF CANCER, 2004, 110 (06) :815-824
[8]   Long-term biochemical disease-free and cancer-specific survival following anatomic radical retropubic prostatectomy - The 15-year Johns Hopkins experience [J].
Han, M ;
Partin, AW ;
Pound, CR ;
Epstein, JI ;
Walsh, PC .
UROLOGIC CLINICS OF NORTH AMERICA, 2001, 28 (03) :555-+
[9]  
Harbeck N, 2002, CANCER RES, V62, P4617
[10]  
HENSON DE, 1994, ARCH PATHOL LAB MED, V118, P779