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血管生成素和VEGF在人肝细胞癌血管生成作用机制的研究
引用本文:邓伟,梁力建.血管生成素和VEGF在人肝细胞癌血管生成作用机制的研究[J].中国普通外科杂志,2005,14(6):12-440.
作者姓名:邓伟  梁力建
作者单位:中山大学附属第一医院,肝胆外科,广东,广州,510080
摘    要:目的探讨血管生成素(Ang)及受体Tie-2、血管内皮牛长因子(VEGF)在肝细胞癌血管生成和进展中的作用。方法用RT-PCR和免疫组织化学方法分析28例肝细胞痛(HCC)、10例肝硬化和10例正常肝标本。观察血管生成素及受体、VEGF的表达与HCC肿瘤血管生成和临床病理的关系。结果Ang/Tie-2,VEGF在肝细胞癌表达明显上调,免疫组织化学也显示Ang-2和VEGF,Tie-2蛋白在肝癌表达增强。Ang-2/Ang-1 mRNA比值、VEGF mRNA与肿瘤血管侵犯及CD34染色的微血管密度相关。结论Ang/Tie-2,VEGF、在HCC肿瘤血管生成和进展中起重要作用。

关 键 词:肝肿瘤  血液供给  肝细胞癌  血液供给  血管生成素  血管内皮生长因子
文章编号:1005-6947(2005)06-0436-05
收稿时间:2005-4-7
修稿时间:2005年4月7日

Effects of angiopioetins/Tie-2 and VEGF expression on hepatocellular carcinoma angiogenesis
DENG Wei,LIANG li jian.Effects of angiopioetins/Tie-2 and VEGF expression on hepatocellular carcinoma angiogenesis[J].Chinese Journal of General Surgery,2005,14(6):12-440.
Authors:DENG Wei  LIANG li jian
Affiliation:Department of Hepatobiliary Surgery, The First Affiliated Hospital, SUN Yat Sen University, Guangzhou 510080, China
Abstract:Objective To investigate the effects of angiopioetins and tyrosine kinase receptor Tie-2 ,vascular endothelial growth factor (VEGF)on the angiogenesis and progression of hepatocellular carcinoma(HCC). Methods With the methods of RT-PCR and immunohistochemistry, the specimens from 28 HCC patients, 10 cirrhotics, and 10 normal livers were analysed, and the relationship between angiopioetins, VEGF (expression) and the clinical pathological characteristics of HCC was studied. Results Ang/Tie-2 and VEGF were significantly up-regulated in HCC compared to cirrhotic tissue and normal liver tissue. (Immunohistochemical) staining also showed increased expression of Ang-2,VEGF,Tie-2 protein in HCC. A high Ang-2/Ang-1mRNA ratio and high VEGF in HCC were closely associated with tumor vascular invasion and microvascular density level which assesssed by CD34. Conclusions Ang /Tie-2 and VEGF may play critical roles in promoting tumor angiogenesis and progression in human HCC.
Keywords:Liver neoplasms/blood supply  Hepatocellular Carcinoma/blood supply  Angiopioetins  VEGF
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