Suppr超能文献

1 型纤溶酶原激活物抑制剂(PAI-1)在透明细胞肾细胞癌(CCRCC)中的表达及其对血管生成、进展和根治性肾切除术后患者生存的影响。

Type 1 plasminogen activator inhibitor (PAI-1) in clear cell renal cell carcinoma (CCRCC) and its impact on angiogenesis, progression and patient survival after radical nephrectomy.

机构信息

Department of Surgical Sciences, University of Bergen, Norway.

出版信息

BMC Urol. 2010 Dec 3;10:20. doi: 10.1186/1471-2490-10-20.

Abstract

BACKGROUND

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.

METHODS

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%).

RESULTS

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.

CONCLUSIONS

PAI-1 was found to be an independently significant prognosticator of CSS and a promoter of tumour angiogenesis, aggressiveness and progression in CCRCC.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f0d/3002359/48d5388943b2/1471-2490-10-20-1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验