Id-1在子宫内膜腺癌中的表达及与VEGF、TSP-1的关系  被引量:3

Expression of Id-1 in the Endometrial Adenocarcinoma and its Correlation with VEGF and TSP-1

在线阅读下载全文

作  者:黄玉秀[1] 郑秀[1] 刘林芳[1] 

机构地区:[1]福建医科大学附属第一医院妇产科,福州350005

出  处:《福建医科大学学报》2009年第3期231-233,240,共4页Journal of Fujian Medical University

基  金:福建省卫生厅青年科研基金(2006-2-4)

摘  要:目的探讨DNA结合抑制蛋白(Id-1)在子宫内膜腺癌组织中的表达以及与血管内皮生长因子(VEGF)、血小板反应素-1(TSP-1)的关系。方法免疫组织化学法检测56例子宫内膜腺癌、18例子宫内膜不典型增生、20例正常子宫内膜组织中Id-1及VEGF、TSP-1蛋白的表达;图像分析软件进行量化处理。结果子宫内膜癌组织中Id-1表达高于正常子宫内膜组织及子宫内膜不典型增生(P<0.05),且与组织分化程度及浸润肌层深度、手术病理分期有关(P<0.05)。子宫内膜癌组织中Id-1与VEGF表达呈正相关性(r=0.318,P=0.017),与TSP-1呈负相关(r=-0.453,P=0.000)。Id-1表达与生存时间无关(P>0.05)。结论Id-1在子宫内膜腺癌中存在着过表达;抑制TSP-1和促进VEGF可能是Id-1参与子宫内膜腺癌的发生发展的一个机制。Objective To study the expressiort of inhibitors of DNA binding-1 (Id-1) in endometrial adenocarcinoma and its correlation with VEGF, TSP-1. Methods By using immunohistochemistry and image analysis, the expressions of Id-1, VEGF and TSP-1 proteins Were studied in a group of 56 patients with endometrial adenocarcinoma, 18 patients with atypia hyperplasia and 20 patients with normal endometria. Results The expression of Id-1 in endometrial adenocarcinoma tissues was significantly higher than that in normal endometria and atypia hyperplasia tissues(P〈0.05) and was significantly correlated with the histological grades, depth of myometrial invasion and clinical stage (all P〈0.05). Id-1 expression in endometrial adenoearcinoma tissues was positively correlated with VEGF expression(r = 0.318, P=0.017)and negatively correlated with TSP-1 expression(r=-0. 453, P=0. 000). No signifi- cant association was found between Id-1 expression and patients' survival time. Conclusions Overexpression of Id-1 is common in endometrial adenocarcinoma. Id-1 might be related to the carcinogenesis and progression of endometrial adenocarcinoma by decreasing TSP-1 expression and increasing VEGF expression.

关 键 词:抑制蛋白 子宫内膜肿瘤 血管内皮生长因子类 血小板 反应素类 

分 类 号:R737.330.22[医药卫生—肿瘤] R392.31[医药卫生—临床医学]

 

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