肝癌组织中VHL表达及其临床意义
详细信息    查看全文 | 推荐本文 |
  • 英文篇名:Expression and Clinical significance of VHL in Hepatocellular carcinoma
  • 作者:陈江明 ; 刘付宝 ; 谢胜学 ; 余立权 ; 耿小平
  • 英文作者:CHEN Jiang-ming;LIU Fu-bao;XIE Sheng-xie;The Second Hospital of Anhui Medical University;
  • 关键词:von ; Hippel-Lindau ; 肝细胞肝癌
  • 英文关键词:von Hippel-Lindau;;hepatocellular carcinoma
  • 中文刊名:GDWZ
  • 英文刊名:Journal of Hepatobiliary Surgery
  • 机构:安徽医科大学第二附属医院;
  • 出版日期:2016-12-31
  • 出版单位:肝胆外科杂志
  • 年:2016
  • 期:v.24
  • 基金:安徽医科大学校校基金(项目编号:2015xkj022)
  • 语种:中文;
  • 页:GDWZ201606021
  • 页数:4
  • CN:06
  • ISSN:34-1143/R
  • 分类号:74-77
摘要
目的讨论肝癌组织中希佩尔林道(von Hippel-Lindau,VHL)的表达及其临床意义。方法采用免疫组化两步法检测VHL蛋白在40例肝癌患者癌组织和癌旁组织及10例正常肝组织中的表达,并分析VHL蛋白的表达与临床指标的关系。结果肝癌组织中VHL表达阳性率(45%)显著低于对应癌旁组织(82.5%)(χ~2=12.17,P<0.0001)。正常肝组织中VHL表达阳性率90%。VHL蛋白的表达与血管侵犯显著相关。肝癌组织中VHL表达阳性和阴性1年、3年、5年的总体生存率分别为83.3%、61.1%、55.5%和59.1%、50%、40.9%,差异无统计学意义(P=0.228)。结论 VHL蛋白在肝癌中的表达与肿瘤的生物学行为及预后密切相关。
        Objective To investigate the expression and clinical significance of von Hippel-Lindau protein in hepatocellular carcinoma. Methods Immunohistochemistry was used for detecting the expression of VHL in HCC tissues(n = 40) and normal hepatic tissues(n = 10). We also analyzed the relationships between the expression of VHL and the clinical characteristics. Results The positive rate of VHL was significantly lower in HCC tissues(45%)than that in paired nocancerous tissue(82. 5%; χ~2= 12. 17,P <0. 0001) and normal hepatic tissues(90%,P = 0. 014). The positive rate of VHL was significantly lower in the vascular invasion groups.The cumulative survival rates at 1,3,5 year VHL positive expression group and VHL negative expression group were 83. 3%,61. 1%,55. 5% and 59. 1%,50%,40. 9%,respectively. Conclusions The expression of VHL are closely related with the biological behavior and prognosis of HCC.
引文
1 Chen W,Zheng R,Baade PD,et al.Cancer statistics in China,2015.CA Cancer J Clin.2016;66(2):115-32.
    2 Findeis-Hosey JJ,Mc Mahon KQ,Findeis SK.Von Hippel-Lindau Disease.J Pediatr Genet.2016;5(2):116-23.
    3 Frew IJ,Krek W.p VHL:A Multipurpose Adaptor Protein.Science Signaling,2008,1,pe30.
    4 Liang Y,Zheng T,Song R,et al.Hypoxia-mediated sorafenib resistance can be overcome by EF24 through Von Hippel-Lindau tumor suppressor-dependent HIF-1αinhibition in hepatocellular carcinoma.Hepatology,2013;57(5):1847-57.
    5 Latif F,Tory K,Gnarra J,et al.Identification of the yon Hippel-Lindau disease tumor suppressor gene.Science 1993,260:1317-1320.
    6 Li M,Kim WY.Two sides to every story:the HIF-dependent and HIF-independent functions of p VHL.J Cell Mol Med 2011,15:187-195.
    7 Leisz S,Schulz K,Erb S,et al.Distinct von Hippel-Lindau gene and hypoxia-regulated alterations in gene and protein expression patterns of renal cell carcinoma and their effects on metabolism.Oncotarget,2015,6(13):11395-406.
    8 Zhou Q,Chen T,Ibe JC,et al.Knockdown of von Hippel-Lindau protein decreases lung cancer cell proliferation and colonization.FEBS Lett.2012;586(10):1510-5.
    9 Kivela AJ,Parkkila S,Saarnio J,et al.Expression of von HippelLindau tumor suppressor and tumor-associated carbonic anhydrases IX and XII in normal and neoplastic colorectal mucosa.World J Gastroenterol.2005,11(17):2616-25.
    10 Wang J,Ma Y,Jiang H,et al.Overexpression of von Hippel-Lindau protein synergizes with doxorubicin to suppress hepatocellular carcinoma in mice.J Hepatol.2011,55(2):359-68
NGLC 2004-2010.National Geological Library of China All Rights Reserved.
Add:29 Xueyuan Rd,Haidian District,Beijing,PRC. Mail Add: 8324 mailbox 100083
For exchange or info please contact us via email.