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诱骗受体3在胰腺癌组织中的表达及意义[J]. 肿瘤防治研究, 2013, 40(12): 1143-1146. DOI: 10.3971/j.issn.1000-8578.2013.12.008
引用本文: 诱骗受体3在胰腺癌组织中的表达及意义[J]. 肿瘤防治研究, 2013, 40(12): 1143-1146. DOI: 10.3971/j.issn.1000-8578.2013.12.008
Clinical Signifi cance of Decoy Receptor 3 Expression in Pancreatic Carcinoma[J]. Cancer Research on Prevention and Treatment, 2013, 40(12): 1143-1146. DOI: 10.3971/j.issn.1000-8578.2013.12.008
Citation: Clinical Signifi cance of Decoy Receptor 3 Expression in Pancreatic Carcinoma[J]. Cancer Research on Prevention and Treatment, 2013, 40(12): 1143-1146. DOI: 10.3971/j.issn.1000-8578.2013.12.008

诱骗受体3在胰腺癌组织中的表达及意义

Clinical Signifi cance of Decoy Receptor 3 Expression in Pancreatic Carcinoma

  • 摘要: 目的 探讨诱骗受体3(decoy receptor,DcR3)在胰腺癌组织中的表达及其与预后生存的相关性。方法 通过免疫组织化学和ELISA分别检测组织和血清中DcR3蛋白的表达,并分析其与预后生存的关系。结果 DcR3阳性细胞染色定位于胞质中,胰腺癌组织中DcR3阳性率为50 %(25/50),而非癌胰腺组织中DcR3阳性率为24%(12/50),两者差异有统计学意义(P<0.05)。术前胰腺癌患者血清中DcR3为(73.71±18.26)pg/ml,与胰腺囊腺瘤组(7.96±1.25)pg/ml相比,差异有统计学意义(P<0.01)。胰腺癌组术后DcR3水平(19.76±4.52)pg/ml明显下降,与术前相比,有统计学差异(P<0.01)。50例随访患者中位生存时间为27.4月。DcR3在血清中的表达水平与患者术后总体生存时间有关 (P<0.05)。Cox回归分析显示与胰腺癌患者总体生存时间相关的指标有肿瘤大小、TNM分期、淋巴转移和血清中DcR3的表达水平。结论 (1)胰腺癌组织和血清中DcR3蛋白高表达;(2)胰腺癌患者血清中DcR3的水平将有助于肿瘤的临床诊断和预后判断。

     

    Abstract: Objective To investigate the expression of DcR3 and correlation between DcR3 and prognosis in pancreatic carcinoma. Methods DcR3 protein expressions in tissues and sera were respectively detected by i mmunohistochemistry(IHC) and ELISA. Correlations between DcR3 expression and prognosis were analyzed. Results DcR3 staining positive cells were located in cytoplasm. The positive rate of DcR3 in pancreatic carcinoma tissues was 50 % (25/50) higher than that in non-cancerous tissues was (24%, 12/50), (P < 0.05). The level of DcR3 in serum of pancreatic carcinoma before operation was (73.71±18.26)pg/ml, showing a signifi cant difference compared to cystadenoma(7.96±1.25) pg/ml (P<0.01),and signifi cantly decreased after operation (19.76±4.52) pg/ml, P < 0.01.The median survival time of these patients was 27.4 months. Patients with higher levels of DcR3 had signifi cantly shorter survival time than those with lower levels of DcR3(P <0.05). The cox regression analysis showed tumor size, TNM stage, lymph node metastasis, and levels of DcR3 were associated with survival. Conclusions DcR3 protein was over-expressed in tissues and sera of pancreatic carcinoma. DcR3 in serum should be considered as a novel parameter for clinical diagnosis and prognostic judgement in pancreatic carcinoma.

     

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