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肝细胞癌尿激酶型纤溶酶原激活物受体mRNA、VEGF和c-erbB2的表达及意义
引用本文:吕小平,詹灵凌,姜海行,唐国都,梁水庭. 肝细胞癌尿激酶型纤溶酶原激活物受体mRNA、VEGF和c-erbB2的表达及意义[J]. 临床肝胆病杂志, 2007, 23(1): 36-38
作者姓名:吕小平  詹灵凌  姜海行  唐国都  梁水庭
作者单位:广西医科大学第一附属医院消化内科,广西,南宁,530021;广西医科大学第一附属医院临床检验中心,广西,南宁,530021;广西医科大学第一附属医院肝胆外科,广西,南宁,530021
基金项目:广西科学研究与技术开发计划资助项目(桂科基0143059)
摘    要:探讨尿激酶型纤溶酶原激活物受体(UPAR)mRNA、血管内皮细胞生长因子(VEGF)和癌基因c—erbB2在肝细胞癌(HCC)的表达与其病理学特性和肿瘤转移的关系。采用原位杂交方法检测肝细胞癌UPA mRNA表达,免疫组化法检测VEGF和c—erbB2的表达。肝癌转移组的UPAR mRNA、VEGF和c—erbB2阳性表达率及表达强度均明显高于无转移组,二者相比均有显著性差异(P〈0.05),但它们的表达与肝癌的大小、分化程度却无关;UPAR mRNA与VEGF及c—erbB2的表达强度均呈正相关(r=0.656、0.653,P〈0.05)。UPA mRNA、VEGF和c—erbB2的表达可作为肝细胞癌的侵袭表型、判断疗效以及估计预后的重要指标。

关 键 词:肝细胞癌  癌基因  尿激酶受体  原位杂交  免疫组化
文章编号:1001-5256(2007)01-0036-03
收稿时间:2005-12-19
修稿时间:2006-01-09

Expression and significance of UPAmRNA, VEGF and c - erbB2 in hepatocellular carcinoma
LU Xiao - ping, ZHAN Ling -ling, JIANG Hai -xing,et al.. Expression and significance of UPAmRNA, VEGF and c - erbB2 in hepatocellular carcinoma[J]. Chinese Journal of Clinical Hepatology, 2007, 23(1): 36-38
Authors:LU Xiao - ping   ZHAN Ling -ling   JIANG Hai -xing  et al.
Affiliation:Department of Gastroenterology, First Affiliated Hospital, Guangxi Medical University, Nanning 530021, China
Abstract:To investigate the expression of urokinase type plasminogen activator receptor(UPAR) mRNA,VEGF and c-erbB2 and to evaluate the relationship between them and pathological properties and metastasis of hepatocellular carcinoma(HCC).The expression of UPAmRNA was detected by in situ hybridization,VEGF and c-erbB2 tested by immunohistochemical assay.The expression rates of UPAR mRNA,VEGF and c-erbB2 tested by immunohistochemical assay.The expression rates of UPAR mRNA,VEGF and c-erbB2 were obviously higher in HCC with metastasis than those in HCC without metastasis(P<0.05).But their expressions were not closely related to tumor size or degree of differentiation.There was a significant relationship between UPAR mRNA,VEGF and c-erbB2 in HCC(r=0.656,0.653,P<0.05).The expression of UPAR mRNA,VEGF and c-erbB2 may be important indexes on evaluating treatment and prognosis of HCC.
Keywords:hepatocellular carcinoma   oncogenes   urokinase type plasminogen activator receptor   in situ hybridization   immunohistochemistry
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