Gong S J, Rha S Y, Chung H C, Yoo N C, Roh J K, Yang W I, Lee K S, Min J S, Kim B S, Chung H C
Department of Internal Medicine, Eulji Medical Center, Eulji Hospital, Seoul, Korea.
Int J Mol Med. 2000 Sep;6(3):301-5.
Cancer invasion is induced by several proteolytic enzyme systems associated with the destruction of basement membrane and extracellular matrix. Urokinase-type plasminogen activator (uPA) and plasminogen activator inhibitor-1 (PAI-1) have been reported as prognostic factors in breast cancer patients and plasminogen activation is regulated by various factors such as uPAR and growth factors. Thus, we examined the tissue levels of urokinase-type plasminogen activator receptor (uPAR) in breast cancer patients. Tissue uPAR levels were measured by ELISA assay in 268 breast cancer patients. The median and mean values of tissue uPAR level in breast cancer were 3.5 ng/mg cytosol protein and 4.8+/-3.6 ng/mg cytosol protein, respectively. Tissue uPAR level was the highest in T1 stage, but there was no statistical significance between the T stages (p>0.05), nor in nodal stage, in the value of uPAR according to progression. And the value of uPAR expression was not associated with estrogen and progesterone receptor status, number of involved node and percent of node involvement. In TNM stage, tissue uPAR levels were higher in patients with stage I-II than in patients with stage III-IV (p=0.027). In univariate analysis, nodal factor (p=0.002) and TNM stage (p=0.0004) were significant. But, multivariate analysis showed that TNM stage was the only significant prognostic factor (p=0.0002). These results suggest that uPAR is mainly associated with initial tumor invasion and other factors might be involved in later stages of cancer progression.
癌症侵袭是由几种与基底膜和细胞外基质破坏相关的蛋白水解酶系统所诱导的。尿激酶型纤溶酶原激活物(uPA)和纤溶酶原激活物抑制剂-1(PAI-1)已被报道为乳腺癌患者的预后因素,并且纤溶酶原激活受多种因素调节,如uPAR和生长因子。因此,我们检测了乳腺癌患者组织中尿激酶型纤溶酶原激活物受体(uPAR)的水平。通过ELISA法检测了268例乳腺癌患者的组织uPAR水平。乳腺癌组织uPAR水平的中位数和平均值分别为3.5 ng/mg胞浆蛋白和4.8±3.6 ng/mg胞浆蛋白。组织uPAR水平在T1期最高,但根据分期,T分期之间(p>0.05)以及淋巴结分期的uPAR值均无统计学意义。并且uPAR表达值与雌激素和孕激素受体状态、受累淋巴结数量及淋巴结受累百分比无关。在TNM分期中,I-II期患者的组织uPAR水平高于III-IV期患者(p=0.027)。单因素分析显示,淋巴结因素(p=0.002)和TNM分期(p=0.0004)具有显著性。但是,多因素分析表明TNM分期是唯一具有显著性的预后因素(p=0.0002)。这些结果提示,uPAR主要与肿瘤的初始侵袭相关,而其他因素可能参与癌症进展的后期阶段。