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结直肠癌组织E-钙黏附素蛋白表达与甲基化的关系

黄美近 彭慧 杨祖立 康亮 王磊 王辉 刘焕亮 汪建平

中山大学学报(医学科学版)2012,Vol.33Issue(5):630-633,4.
中山大学学报(医学科学版)2012,Vol.33Issue(5):630-633,4.

结直肠癌组织E-钙黏附素蛋白表达与甲基化的关系

Relationship and Significance of Expression of E-cadherin Proteins and Methylation of Promoter in Colorectal Cancer Tissues

黄美近 1彭慧 1杨祖立 1康亮 1王磊 1王辉 1刘焕亮 1汪建平1

作者信息

  • 1. 中山大学附属第六医院//广东省胃肠肛门医院结直肠肛门外科,广东广州510655
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摘要

Abstract

[Objective] To explore the relationship between methylation of promoter and the expression of E-cadherin proteins in colorectal cancer. [Methods] Streptavidin-peroxidase (S-P) two-step method was used to measure the immunohistochemical expression of E-cadherin proteins in 100 CRC. Those slides exhibiting diffuse immunostaining presenting more than 75% of tumor cells were classified as (+++), between 50% and 75% were classified as (++), between 25% and 50% were classified as ( + ) , and those with immunoreactivity less than 10% were classified as (-).(-) and (+) were combine together as lower expression cases, while (++) and (+++) were combined together as higher expression cases for statistical analysis. [Results] The positive rate of E-cadherin proteins was 76% (+~+++) in 100 sporadic colorectal cancer specimen. Fifty-nine cases showed higher expression of E-cadherin, while decreased E-cadherin immunohistochemical expression was observed in 41 cases. The methylation positive rate was 68.3% of E-cadherin was significant association with protein decreased expression of E-cadherin gene (P < 0.001). [Conclusion] Methylation of E-cadherin gene was significant association with E-cadherin protein decreased expression. The loss of E-cadherin protein was one of the important influence factors in colorectal cancer metastatic and invasive.

关键词

E-钙黏附素/免疫组化和甲基化/结直肠癌

Key words

E-cadherin/ immunohistochemical and methylation/ colorectal cancer

分类

医药卫生

引用本文复制引用

黄美近,彭慧,杨祖立,康亮,王磊,王辉,刘焕亮,汪建平..结直肠癌组织E-钙黏附素蛋白表达与甲基化的关系[J].中山大学学报(医学科学版),2012,33(5):630-633,4.

基金项目

广东省科技计划基金(2011B080701064) (2011B080701064)

中山大学学报(医学科学版)

OA北大核心CSCDCSTPCD

1672-3554

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