基础医学与临床 ›› 2014, Vol. 34 ›› Issue (7): 979-983.

• 研究论文 • 上一篇    下一篇

沉默信息调节因子1(SIRT1)在前列腺癌恶性生物学表型中的作用

李淑玲1,王忠利2,王翠瑶3   

  1. 1. 辽宁医学院
    2. 辽宁医学院附属一院
    3. 辽宁医学院基础医学院
  • 收稿日期:2014-02-17 修回日期:2014-05-17 出版日期:2014-07-05 发布日期:2014-06-24
  • 通讯作者: 王翠瑶 E-mail:1140379451@qq.com
  • 基金资助:
    辽宁省教育厅一般项目资助课题

Role of silent information regulator 1(SIRT1) in the malignant biological behavior of prostate cancer

  • Received:2014-02-17 Revised:2014-05-17 Online:2014-07-05 Published:2014-06-24

摘要: 目的 观察SIRT1在前列腺癌组织和细胞中的表达,探讨SIRT1在前列腺癌发生中的作用。方法 收集辽宁医学院附属第一医院手术切除的8例成对前列腺癌组织和癌旁组织随机分组,体外培养PrEC、LNCap、PC3和DU145细胞,Real-time PCR和Western blot法检测SIRT1和P53在前列腺癌组织和细胞中mRNA和蛋白表达。提取细胞系中总蛋白、浆蛋白和核蛋白,Western blot法检测PC3和DU145细胞中SIRT1和P53的蛋白表达和定位。结果 前列腺癌组织中,SIRT1的mRNA和蛋白表达明显高于癌旁组织(P<0.01);LNCap、PC3和DU145细胞中SIRT1的mRNA和蛋白表达明显高于PrEC细胞(P<0.01);PC3和DU145细胞核SIRT1蛋白表达明显高于胞质(P<0.01)。结论 SIRT1可能通过P53不同方式促进前列腺癌发生,为探讨SIRT1在前列腺癌恶性生物学表型中的作用和机制奠定基础。

关键词: 沉默信息调节因子1, 前列腺癌, p53, PC3, DU145

Abstract: Objective To detect the expression of silent information regulator 1(SIRT1)in the clinical prostate cancer tissues and cells, and to explore the role of SIRT1 in the development of prostate cancer. Methods A total of 8 human prostate adenocarcinoma tissues and adjacent normal prostate tissues were acquired from the First Affiliated Hospital of Liaoning Medical University and the SIRT1 and P53 mRNA and protein expression levels in prostate tissues were determined by Real-time PCR and Western blot. The normal human prostate epithelial cells PrEC and human prostate carcinoma cell lines LNcap, PC3and DU145 were cultured in vitro, then the SIRT1 and P53 mRNA expression levels were detected by real-time PCR. The whole cell protein lysates, nuclear and cytosolic protein lysates were prepared for Western blot to determine the SIRT1 and P53 protein expression levels in PC3 and DU145 cells. Results SIRT1 was found to be overexpressed in human prostate cancer tissues compared with adjacent normal prostate tissue(P<0.01). SIRT1 was significantly overexpressed in human prostate cancer cells LNcap, PC3 and DU145 compared with PrEC cells at mRNA and protein levels (P<0.01)and SIRT1 was predominantly localized in the nuclear of PC3 and DU145 cells(P<0.01). Conclusion Nuclear SIRT1, via P53 dependent and independent activation, could contribute to the development of prostate cancer, and pay a foundation for exploring the possible role and underlying mechanisms of SIRT1 on the malignant behavior of prostate cancer.

Key words: silent information regulator 1(SIRT1), prostate cancer, p53, PC3, DU145