HMGB1在肝细胞癌中的表达及其与VEGF、MVD的关系  被引量:12

Correlations of HMGB1 expression with VEGF and microvascular density in hepatocellular carcinoma

在线阅读下载全文

作  者:周宝勇[1] 郑军[1] 侯俊丞[1] 黄军伟[1] 

机构地区:[1]重庆医科大学附属第一医院肝胆外科,重庆400016

出  处:《重庆医科大学学报》2012年第5期409-412,共4页Journal of Chongqing Medical University

摘  要:目的:探讨高迁移率族蛋白1(High mobility group protein box-1,HMGB1)在肝细胞癌组织中的表达及其与血管内皮生长因子(Vascular endothelial growth factor,VEGF)表达、肿瘤微血管密度(Microvascular density,MVD)的关系和临床意义。方法:免疫组织化学SP法检测HMGB1、VEGF和CD34在37例人肝癌组织及相应癌旁肝组织和10例人正常肝组织中的表达;并用抗CD34抗体标记微血管,计数微血管密度;应用Western blot技术定量检测HMGB1在10例肝癌及相应癌旁和5例正常肝组织的表达情况。结果:HMGB1蛋白在肝癌组织中的表达明显高于癌旁组织及正常肝组织。HMGB1的表达与肿瘤大小、门静脉侵犯相关(P=0.018;P=0.036)。肝癌组织中HMGB1表达与VEGF表达及MVD间均呈正相关(r=0.544,P=0.001;r=0.672,P<0.05)。结论:肝癌组织中异常表达增高的HMGB1、VEGF与肝癌微血管生成过程相关,HMGB1可能成为阻断肝癌血管生成的有效靶点。Objective:To investigate the correlations of high mobility group protein box-1(HMGB1) expression with vascular endothelial growth factor(VEGF) expression and microvessel density(MVD) in hepatocellular carcinoma(HCC) and its clinical significance.Methods: Expressions of HMGB1,VEGF and CD34 were detected with immunohistochemistry in 37 specimens of HCC tissues and the corresponding adjacent-tumor tissues,and 10 cases of normal hepatic tissues.The MVD was calculated using CD34 antibody as an endothelial marker.Western blot was performed in 10 HCC tissues and the corresponding adjacent-tumor tissues,and 5 normal hepatic tissues.Results: Expression of HMGB1 appeared at a high level compared to adjacent-tumor tissues and normal hepatic tissues.HMGB1 expression was significantly correlated with the tumor size and the portal venous invasion.HMGB1 expression was positively correlated with VEGF expression and MVD in HCC(r=0.544,P=0.001;r=0.672,P0.05).Conclusion: Upregulation of HMGB1 and VEGF are involved in the angiogenesis of HCC,and HMGB1 may be a therapeutic target for angiogenesis in HCC.

关 键 词:肝癌 高迁移率族蛋白1 血管内皮生长因子 微血管密度 

分 类 号:R735.7[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象