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Thrombomodulin Expression in Bladder Cancer Tissue and Its Association with Prognosis and Patient Survival

机译:膀胱癌组织中的血栓调节蛋白表达及其与预后和患者存活的关联

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Background: Decreased expression of thrombomodulin (TM) in bladder cancer tissue has been shown to be associated with cell proliferation, increased malignancy and a poor prognosis. The aim of this study was to investigate the immunoexpression of TM in bladder tissue cores by immunohistochemistry (IHC) and the relationship between TM score and patient survival for the following pathologies: transitional cell papillary carcinoma (TCPC), transitional cell carcinoma (non-papillary) (TCC), squamous cell carcinoma (SCC), adenocarcinoma, and sarcoma. TM immunoexpression was also evaluated in normal adjacent bladder tissue cores. Methods: TM immunoexpression was assessed in n=185 formalin-fixed paraffin-embedded (FFPE) bladder tissue cores from n=98 patients by IHC. Tissue cores included TCPC (n=29), TCC (n=85), SCC (n=21), adenocarcinoma (n=12), sarcoma (n=4), and normal tissue cores (n=34). Results: TM immunoexpression scores are stronger in TCPC, TCC and SCC bladder cancer tissue?cores with respect to adenocarcinoma and sarcoma (mean TM immunoexpression scores: 3.04, 2.57, 2.55, 1.55 and 1.19, respectively) (Kruskal–Wallis p 0.001). TM immunoexpression scores significantly decreased in bladder cancer tissue cores across both stage (p 0.001) and grade (p 0.001) (Kruskal–Wallis). Survival data were available for n=45 bladder cancer patients (mean follow-up of 34 months). Applying a TM immunoexpression cut-off score of 3.0 demonstrated that patients with bladder cancer who had a TM immunoexpression score 3.0 had lower survival rates (median survival 23.5 months). In contrast, patients with TM immunoexpression scores ≥ 3.0 had longer survival rates (median survival 40 months) (log-rank; p=0.045). Conclusion: TM immunoexpression in bladder cancer tissue may be a clinically relevant predictor of tumor progression and survival. Low expression of TM in bladder cancer biopsies or in recurrent bladder cancer may be indicative of a poor prognosis. TM immunoexpression could be used to guide clinical decision making.
机译:背景:膀胱癌组织中血栓调节蛋白(TM)的表达减少已被证明与细胞增殖相关,恶性肿瘤增加和预后不良。本研究的目的是通过免疫组织化学(IHC)来研究膀胱组织核心的TM免疫表达和TM评分与患者存活的关系:过渡细胞乳头状癌(TCPC),过渡细胞癌(非乳头状)(TCC),鳞状细胞癌(SCC),腺癌和肉瘤。在正常相邻的膀胱组织核中也评估了TM免疫表达。方法:在N = 185型固定石蜡包埋(FFPE)膀胱组织核中评估TM免疫表达,由IHC患者的N = 98例。组织核包括TCPC(n = 29),TCC(N = 85),SCC(n = 21),腺癌(n = 12),肉瘤(n = 4)和正常组织核(n = 34)。结果:TM免疫表达分数在TCPC,TCC和SCC膀胱癌组织中较强?相对于腺癌和肉瘤的核心(平均TM免疫表达分数:3.04,2.57,2.55,1.55和1.19)(Kruskal-Wallis P <0.001) 。 TM免疫表达在膀胱癌组织核上横跨两级(P <0.001)和等级(P <0.001)(Kruskal-Wallis)显着降低。可用于N = 45膀胱癌患者的存活数据(平均34个月)。应用TM免疫表达截止得分3.0证明,膀胱癌的患者患有TM免疫表达得分<3.0的存活率降低(中位生存率23.5个月)。相比之下,TM免疫表达评分≥3.0的患者体育率较长(中位存活40个月)(对数级别; P = 0.045)。结论:膀胱癌组织中的TM免疫表达可能是肿瘤进展和存活的临床相关预测因子。在膀胱癌活检或复发性膀胱癌中表达TM的低表达可能表明预后差。 TM免疫表达可用于指导临床决策。

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