Stephens R W, Nielsen H J, Christensen I J, Thorlacius-Ussing O, Sørensen S, Danø K, Brünner N
The Finsen Laboratory, Rigshospitalet, Copenhagen, Denmark.
J Natl Cancer Inst. 1999 May 19;91(10):869-74. doi: 10.1093/jnci/91.10.869.
The proteolytic enzyme plasmin, which is generated from the precursor plasminogen by the action of urokinase plasminogen activator, is thought to play a role in tumor cell invasion and metastasis. Urokinase plasminogen activator receptor (uPAR) is functionally involved in the cell surface activation (i.e., cleavage) of plasminogen. Increased tumor tissue levels of uPAR are associated with poor prognosis in several types of cancer. This retrospective study was undertaken to test the relationship between preoperative plasma levels of soluble uPAR (suPAR) and survival in patients with colorectal cancer.
suPAR levels in preoperative plasma from 591 patients with colorectal cancer were determined by use of a kinetic enzyme-linked immunosorbent assay and analyzed with respect to associations with postoperative survival, Dukes' stage, age, and serum carcinoembryonic antigen level. Plasma suPAR measurements were log transformed for survival analysis, which employed the Kaplan-Meier method and the Cox proportional hazards model. All P values reported are two-sided.
Univariate analysis, using the log-transformed suPAR concentrations, demonstrated that there was an increasing risk of mortality with increasing plasma suPAR level (P<.0001). An arbitrary cut point, the median for all patients (1.37 ng/mL), divided patients with Dukes' stage B, C, or D disease into statistically different prognostic groups. In multivariate Cox analysis including Dukes' stage, age, and carcinoembryonic antigen level, the suPAR concentration independently predicted survival (P<.0001).
The preoperative plasma suPAR level independently predicted survival of patients with colorectal cancer. Further studies of plasma suPAR in patients with cancer are needed to evaluate the utility of plasma suPAR measurements and cut points in identifying high-risk patients among those with early stage disease.
纤溶酶是一种蛋白水解酶,由尿激酶型纤溶酶原激活剂作用于纤溶酶原前体产生,被认为在肿瘤细胞侵袭和转移中起作用。尿激酶型纤溶酶原激活剂受体(uPAR)在纤溶酶原的细胞表面激活(即裂解)过程中发挥功能作用。多种癌症中,肿瘤组织uPAR水平升高与预后不良相关。本回顾性研究旨在检测结直肠癌患者术前血浆可溶性uPAR(suPAR)水平与生存之间的关系。
采用动力学酶联免疫吸附测定法测定591例结直肠癌患者术前血浆中的suPAR水平,并分析其与术后生存、Dukes分期、年龄和血清癌胚抗原水平的相关性。血浆suPAR测量值进行对数转换以进行生存分析,生存分析采用Kaplan-Meier法和Cox比例风险模型。所有报告 的P值均为双侧。
使用对数转换后的suPAR浓度进行单因素分析表明,血浆suPAR水平升高,死亡风险增加(P<0.0001)。以所有患者的中位数(1.37 ng/mL)作为任意切点,可将Dukes分期为B、C或D期疾病的患者分为具有统计学差异的预后组。在包括Dukes分期、年龄和癌胚抗原水平的多因素Cox分析中,suPAR浓度可独立预测生存(P<0.0001)。
术前血浆suPAR水平可独立预测结直肠癌患者的生存情况。需要对癌症患者的血浆suPAR进行进一步研究,以评估血浆suPAR测量值和切点在识别早期疾病高危患者中的效用。