Department of Surgical Sciences, University of Bergen, Norway.
BMC Urol. 2010 Dec 3;10:20. doi: 10.1186/1471-2490-10-20.
To examine the expression of type 1 plasminogen inhibitor (PAI-1) in clear cell renal cell carcinoma (CCRCC), and its possible association with microvessel density (MVD), the expression of thrombospondin-1 (TSP-1), nuclear grade, tumour stage, continuously coded tumour size (CCTS) and to assess the value of PAI as a prognostic marker in 162 patients with CCRCC treated with radical nephrectomy.
A total of 172 consecutive patients with CCRCC treated with radical nephrectomy were enrolled in the study. The expression of PAI-1, TSP-1 and factor VIII were analysed on formalin-fixed, paraffin-embedded tissues without knowledge of the clinical outcome. Ten cases, where PAI-1 immunohistochemistry was not possible due to technical problems and lack of material, were excluded. Sixty-nine patients (43%) died of RCC, while 47 patients (29%) died of other diseases. Median follow-up was 13.8 years for the surviving 46 patients (28%).
Nine percent of the tumours showed PAI-1 positivity. High expression of PAI-1 was significantly inversely correlated with TSP-1 (p = 0.046) and directly with advanced stage (p = 0.008), high NG (3+4) (p = 0.002), tumour size (p = 0.011), microvessel density (p = 0.049) and disease progression (p = 0.002). In univariate analysis PAI-1 was a significant prognosticator of cancer-specific survival (CSS) (p < 0.001). Multivariate analysis revealed that TNM stage (p < 0.001), PAI-1 (p = 0.020), TSP-1 (p < 0.001) and MVD (p = 0.007) were independent predictors of CSS.
PAI-1 was found to be an independently significant prognosticator of CSS and a promoter of tumour angiogenesis, aggressiveness and progression in CCRCC.
为了研究 1 型纤溶酶原抑制剂(PAI-1)在透明细胞肾细胞癌(CCRCC)中的表达及其与微血管密度(MVD)、血小板反应蛋白-1(TSP-1)、核分级、肿瘤分期、连续编码肿瘤大小(CCTS)的可能相关性,并评估 PAI-1 在 162 例接受根治性肾切除术的 CCRCC 患者中的预后价值。
本研究共纳入 172 例接受根治性肾切除术的 CCRCC 连续患者。在不了解临床结果的情况下,对福尔马林固定、石蜡包埋组织中的 PAI-1、TSP-1 和因子 VIII 的表达进行了分析。由于技术问题和缺乏材料,10 例 PAI-1 免疫组化无法进行的病例被排除在外。69 例(43%)患者死于 RCC,47 例(29%)患者死于其他疾病。46 例存活患者(28%)的中位随访时间为 13.8 年。
9%的肿瘤呈 PAI-1 阳性。高表达 PAI-1 与 TSP-1(p = 0.046)和晚期(p = 0.008)、高核分级(3+4)(p = 0.002)、肿瘤大小(p = 0.011)、微血管密度(p = 0.049)和疾病进展(p = 0.002)呈显著负相关。在单因素分析中,PAI-1 是癌症特异性生存(CSS)的显著预后因素(p < 0.001)。多因素分析显示,TNM 分期(p < 0.001)、PAI-1(p = 0.020)、TSP-1(p < 0.001)和 MVD(p = 0.007)是 CSS 的独立预测因素。
PAI-1 是 CCRCC CSS 的独立显著预后因素,也是肿瘤血管生成、侵袭性和进展的促进因素。