期刊文献+

肝外胆管癌组织中HIF-1α、VEGF的表达及其相关性

Expression and relationship of HIF-1α and VEGF in extrahepatic cholangiocarcinoma
下载PDF
导出
摘要 目的观察肝外胆管癌组织中缺氧诱导因子-1α(HIF-1α)与血管内皮生长因子(VEGF)的表达及其相关性。方法采用免疫组化SP法检测50例肝外胆管癌及20例正常肝外胆管组织中的HIF-1α及VEGF。结果肝外胆管癌组织中HIF-1α、VEGF表达均明显高于正常肝外胆管组织(P<0.01);二者表达与肝外胆管癌淋巴结转移有关(P<0.05);在肝外胆管癌组织中HIF-1α、VEGF的表达呈正相关(r=0.467,P=0.01)。结论HIF-1α、VEGF在肝外胆管癌组织中均呈高表达,两者对肝外胆管癌的发生、发展及转移有协同作用。 Objective To observe the expression of hypoxia-inducible factor 1 alpha(HIF-1α) and vascular endothelial growth factor(VEGF) in extrahepatic cholangiocarcinoma tissue, and investigate their relationship. Methods The expression of HIF-1α and VEGF were detected by immunohistochemistry SP in 50 cases of extrahepatic cholangiocarcinoma and 20 cases of normal extrahepatic bile duct tissue. Results The expression of HIF-1α and VEGF in extrahepatic cholangiocarcinoma tissue were obviously higher than in normal extrahepatic bile duct tissue( P 〈 0.01 ) ,The expression of HIF-1α and VEGF had no significant relationship with sex,age,tumor size,TNM clinical stage and the degree of differentiation,but which is related to lymph node metastasis( P 〈 0.05 ) ;The expression of HIF-1α and VEGF in extrahepatic cholangiocarcinoma tissue were positive correlation(r = 0.467, P = 0.01 ). Conclusion HIF-1α and VEGF are high expression in extrahepatic cholangiocareinoma tissue, both have synergistic effect in the occurrence of extrahepatic cholangiocarcinoma, development and transfer.
出处 《山东医药》 CAS 北大核心 2009年第34期17-19,共3页 Shandong Medical Journal
关键词 肝外胆管癌 缺氧诱导因子-1Α 血管内皮生长因子 extrahepatic cholangiocarcinoma hypoxia-inducible factor 1 alpha vascular endothelial growth factor
  • 相关文献

参考文献9

  • 1Kaio E,Tanaka S, Kitadai Y, et al. Clinical significance of angiogenie factor expression at the deepest invasive site of advanced colovectal carcinoma[ J ]. Oncology ,2003,64 ( 1 ) :61-73.
  • 2樊利芳,刁路明,陈德基.缺氧诱导因子-1与肿瘤[J].中华病理学杂志,2002,31(2):168-170. 被引量:43
  • 3Bracken CP,Whitelaw ML, Peer DL, The hypoxia-indueible factors: Key transcriptional regulators of hypoxie responses[ J]. Cell Mol Life Sci ,2003,60(7) : 1376-1393.
  • 4Birner P, Schindl M, Obermair A, et al. Overexpression of hypoxia inducible factor-1 alpha is a maker for an unfavorable prognosis in early-stage invasive cervical cancer[ J]. Cancer Res, 2000,60 ( 17 ) : 4693 -4696.
  • 5Schmaltz C, Hardenbergh PH, Wells A, et al. Regulation of proliferation survival decisions during tumor cell hypoxia[ J]. Mol Cell Biol, 1998,18(5) :2845- 2854.
  • 6Kuwai T, Kitadai Y, Tanks S, et al. Expression of hypoxia inducible factor-1 alpha is associated with tumor vascularlzaton in human colorectal carcinoma [ J ]. Int J Cancer, 2003, 105 ( 2 ) : 176-181.
  • 7Ryan HE,Poloni M, Menulty W, et al. Hypoxia-inducible factor-1αis a positive factor in solid tumor growth [ J ]. Cancer Rreseach, 2000,60(15) : 4010-4015.
  • 8Werther K, Christensen IJ, Nielsen H J, et al. Prognostic impact of matched preoperative plasma and serum VEGF in patients with primary eoloreetal carcinoma[J]. Br J Cancer,2002,86 (3) : 417- 423.
  • 9Bairey O, Boycov O, Kaganovsky E, et al. All three receptors for vascular endothelial growth factor (VEGF) are expressed on B-chroniclymphocytic leukemia ( CLL ) cells [ J]. Leuk Res,2004,28 (3) : 221-222.

二级参考文献23

  • 1Semenza GL,Agani F,Booth G,et a1.Structural and f un ctional analysis of hypoxia-inducible factor 1.Kidney Int,1997,51:553-555.
  • 2Minet E,Michel G-Remacle P,et al.Role of HIF-1 as a tran scription factor i nvolved in embryonic development,cancer progression and apoptosis.Int J Mol Me d,2000,5:253-259.
  • 3Maxwell PH,Dachs GU,Gleadle JM,et a1.Hypoxia-inducible f actor 1 modulates gene expression in solid tumors and influences both angiogenesis and tumor growt h. Pro Natl Acad Sci U S A,1997,94:8104-8109.
  • 4Boast K,Binley K,Iqbau S,et al.Characterization of physiologi cally regulated v ectors for the treatment of ischemic disease.Human Gene Therapy,1999,10:2197- 2208.
  • 5Okino ST,Chichester CH,Whitlock JP Jr.Hypoxia-inducible mamm alian gene express ion analyzed in vivo at a TATA-driven promoter and at initiator-driven promote r. J Biol Chem, 1998,273:23837-23843.
  • 6Ruan H,Wang J,Hu L,et al. Killing of brain tumor cells by hypoxia-responsive element mediated expression of BAX. Neoplasi a, 1999,1:431-437.
  • 7Suzuki H,Tomida A,Tsuruo T,et al.Dephosphorylated hypoxia-in ducib le factor 1 alpha as a mediator of p53-dependent apoptosis during hypoxia.Oncog e ne,2001,20:5779-5788.
  • 8Bl agosklonny MV,An WG,Romanova LY,et al.p53 inhibits hypoxia-inducible factor-s ti mulated transcription.J Biol Chem,1998,273:11995-11998.
  • 9Ravi R,Mookerjee B,Bh ujwalla ZM,et al.Regulation of tumor,or angiogenesis by p53-induced degradatio n o f hypoxia-inducible factor 1 alpha.Genes Dev,2000,14:34-44.
  • 10Jiang BH,Agani F,Pas saniti A,et al.V-SRC induces expression of hypoxia-inducible factor 1(HIF-1) and transcription of genes encoding vascular endothelial growth factor and enolase 1:involvement of HIF-1 in tumor progression.cancer Res, 1997,57:5328-5335.

共引文献42

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