Shank1 在肾细胞癌组织中的表达及临床意义

Expression of Shank1 and its clinical significance in renal cancer tissue

  • 摘要: 目的:检测Shank 家族成员Shank1 在肾细胞癌(renal cell carcinoma,RCC )中的表达,探讨在RCC 癌组织与癌旁组织中Shank1 的表达差异,分析其与RCC 临床病理特征的关系。方法:收集2008年5 月至2014年12月沧州市中心医院与济南市中心医院120 例RCC 术后患者的癌组织与癌旁组织标本,采用免疫组织化学染色及Westernblot检测Shank1 的蛋白表达水平,分析Shank1 表达与RCC 临床病理特征的关系。结果:免疫组织化学结果显示,RCC 的癌组织中Shank1 表达较癌旁组织明显上调,差异具有统计学意义(P < 0.05)。 Westernblot检测发现RCC 的癌组织中Shank1 蛋白表达水平明显高于癌旁组织。对Shank1 表达上调RCC 患者的临床病理特征分析发现,Shank1 在癌组织中的高表达与患者的性别、年龄、肿瘤的大小、TNM 分期无显著性相关(P > 0.05),但与RCC 的不同病理类型显著性相关(P < 0.05)。 结论:Shank1 在RCC 的癌组织中异常表达,并与RCC 的病理类型相关。

     

    Abstract: Objective:To detect the expression of Shank 1 protein in renal cell carcinoma (RCC), to investigate its difference between the tumor and carcinoma adjacent tissue, and to analyze its correlation with RCC clinicopathological characteristics and prognosis. Methods: The renal carcinoma and carcinoma adjacent tissues of120 patients were selected from Cangzhou Central Hospital and Ji'nan Central Hospital from May 2008 to December 2014 . The expression level of Shank1 was determined by immunohistochemistry and Western blot. Statistical analysis was performed to determine the relationship between the expression of Shank 1 and the clinicopathological features of RCC patients. Results:Results of immunohistochemistry showed that the expression level of Shank1 in renal cancer tissue was significantly higher than that in carcinoma adjacent tissue, and the difference was statistically significant (P<0.05). Western blot results showed that the expression level of Shank 1 protein in renal cancer tissue was also significantly higher than in carcinoma adjacent tissue. Correlation analysis found that the high expression level of Shank 1 in renal cancer tissue was not significantly related to gender, age, tumor size, and TNM stage, but was significantly associated with the histological differentiation of RCC (P<0.05 ). Conclusion: Shank1 is abnormally expressed in RCC renal cancer tissues and is correlated with the histological differentiation of RCC.

     

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