期刊文献+

肝细胞癌中PHD2蛋白与HIF-1α蛋白表达的关系及意义 被引量:5

Expression of PHD2 and HIF-1α in hepatocellular carcinoma and its clinical significance
暂未订购
导出
摘要 目的研究肝癌组织中脯氨酸羟化酶(PHD)2蛋白的表达情况及其与缺氧诱导因子(HIF)-1α蛋白表达和患者临床特征的关系。方法选取肝细胞癌标本80例,应用免疫组织化学染色方法(SP法)研究PHD2蛋白与HIF-1α蛋白的表达情况,并探讨PHD2蛋白的表达与多种临床指标的关系。结果PHD2在肝癌组织中表达的阳性率为47.5%(38/80),与HIF-1α蛋白(66.3%)的表达率无显著差异,但在低分化肝细胞癌组织中的表达率明显高于高分化者,与肿瘤直径和是否有转移或者血管侵犯没有明显关系。结论PHD2虽然是HIF-1α的直接下游基因,但其蛋白表达受多种因素的影响,两者的关系在肝癌组织中没有协同性。以增加肿瘤组织中PHD2的表达降解HIF-1α来治疗肿瘤可能对低分化肿瘤的效果明显。 Objective To investigate the expression of PHD2 and HIF-1α and their clinical significance in human hepatocellular carcinoma. Methods The expression of PHD2 and HIF-1α in 80 cases of HCC were studied by immunohistochemistry assay. Results The expression of PHD2 and HIF-1α were 47. 5%(38/80) and 66. 3% respectively. There was no significant correlation between the expression of the two kinds of protein in HCC by Chi-square test. The increased expression of PHD2 protein is found in less differentiated HCC and is not associated with the diameter of carcinomas and metastasis. Conclusion Although PHD2 is the direct HIF gene, there are no significant relationship between the expression of the two kinds of proteins because there are more other factors to influence the expression of PHD2. In conclusion, it is possible to therapy HCC by adding the expression of PHD2, especially in less differentiated HCC.
出处 《华中医学杂志》 CAS 2008年第2期116-117,129,共3页 Central China Medical Journal
关键词 脯氨酸羟化酶 缺氧诱导因子 免疫组织化学 Prolyl hydroxylase Hypoxia-inducible factor Immunohistochemistry
  • 相关文献

参考文献8

  • 1Seth P, Krop I, Porter D et al. Novel estrogen and tamoxifen induced genes identified by SAGE (serial analysis of gene expression). Oncogene, 2002,21 (5) : 836.
  • 2Bimer P, Schindl M, Oberhuber G. Overexpression of hypoxia-inducible factor-1 alpha is a marker for anunfavorable prognosis in early-stage invasive cervical cancer. Cancer Res,2000,60(18) :4693.
  • 3Berra E,Benizri E,Ginouves A et ak HIF prolyl-hydroxylase 2 is the key oxygen sensor setting low steady-state levels of HIF- 1 a in normoxia. EMBO J, 2003,22 ( 16 ) : 4082.
  • 4Metzen E, Stiehl DP, Doege K et al. Regulation of the prolyl hydroxylase domain protein 2 (phd2/egln-1) gene: identification of a functional hypoxia-responsive element. Biochem J,2005, 387(3) : 711.
  • 5Marxsen JH, Stengel P, Doege K et al. Hypoxia-inducible factor-1 (HIF-1) promotes its degradation by induction of HIF-a-prolyl-4-hydroxylases . Biochem J, 2004, 381(3): 761.
  • 6Yi Pan, Kyle DM, Cara C et al. Multiple Factors Affecting Cellular Redox Status and Energy Metabolism Modulate Hypoxia-Inducible Factor Prolyl Hydroxylase Activity In Vivo and In Vitro. Mol Cell Biol,2007,27(3) : 912.
  • 7Nakayama K, Frew IJ, Hagensen M et al. Siah 2 regulates stability of prolyl-hydroxylases, controls HIF-1α abundance ,and modulates physiological responses to hypoxia. Cell,2004,117(7) :941.
  • 8Manalo DJ, Rowan A, Lavoie T et al. Transcriptional regulation of vascular endothelial cell responses to hypoxia by HIF-1. Blood,2005,105(2) :659.

同被引文献45

引证文献5

二级引证文献23

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部