中国癌症杂志 ›› 2013, Vol. 23 ›› Issue (11): 900-903.doi: 10.3969/j.issn.1007-3969.2013.11.008

• 论著 • 上一篇    下一篇

胃癌患者外周血与胃癌组织中ERCC1基因甲基化的关系及其意义

王红兵1,2,陈卫昌1   

  1. 1.苏州大学附属第一医院消化内科,江苏 苏州, 215006;
    2.徐州医学院附属医院肿瘤内科,江苏 徐州, 221009
  • 出版日期:2013-11-25 发布日期:2014-02-18
  • 通信作者: 陈卫昌 E-mail:wcchen1990@126.com

The relationship between methylation of ERCC1 gene in peripheral blood and in gastric cancer tissues

WANG Hong-bing1,2,CHEN Wei-chang1   

  1. 1.Department of Digestive Disease, The First Affiliated Hospital of Soochow University, Suzhou Jiangsu 215006, China;
    2.Department of Oncology, Affiliated Hospital of Xuzhou Medical College, Xuzhou Jiangsu 221009, China
  • Published:2013-11-25 Online:2014-02-18
  • Contact: CHEN Wei-chang E-mail: wcchen1990@126.com

摘要:

背景与目的:胃癌的发生基于基因和表观遗传学机制,表观遗传学的改变在胃癌的发展中起到重要作用。DNA甲基化是目前研究最多、最为深入的一种表观遗传学表达机制。DNA甲基化是一个可逆性过程。核苷酸切除修复交叉互补基因1(excision repair cross-complementing gene 1ERCC1)是一种DNA损伤修复基因。本研究检测胃癌患者外周血与胃癌组织中ERCC1基因启动子CpG岛甲基化状态,探讨两者的关系及其意义。方法:采用甲基化特异性PCR技术,检测30例胃癌患者外周血、胃癌组织中ERCC1基因启动子CpG岛甲基化状态。结果:胃癌组织中ERCC1基因启动子CpG岛甲基化率为76.7%(23/30),外周血中ERCC1基因启动子CpG岛甲基化率为63.3%(19/30),差异无统计学意义。结论:胃癌患者外周血中的ERCC1基因启动子CpG岛甲基化率与胃癌组织中相似,检测胃癌患者外周血中的ERCC1基因启动子CpG岛甲基化状态为治疗胃癌提供一个简便、快捷、可靠的途径,同时也为以ERCC1基因启动子CpG岛甲基化作为靶点治疗胃癌提供了可靠的理论依据。

关键词: 胃癌, 核苷酸切除修复交叉互补基因1, CpG岛, 甲基化, 甲基化特异性PCR

Abstract:

Background and purpose: At present, gastric cancer is considered to be both genetic and epigenetic disease, and epigenetic alterations play a significant role in the development of gastric cancer. DNA methylation is the most well studied and most in-depth epigenetic modifications in human-beings. The silencing of tumor-related genes by DNA methylation is reversible. ERCC1 is a kind of DNA repair gene. The present study was aimed to detect the CpG island methylation status of ERCC1 gene promoter in gastric cancer tissues and corresponding peripheral blood, and to explore the relationship between methylation of ERCC1 gene in peripheral blood and in gastric cancer tissues. Methods: Methylation specific PCR was performed to detect the methylation status of ERCC1 gene in the tumor tissues and the paired peripheral blood from 30 gastric cancer patients. Results: The positive rate of methylation of ERCC1 gene promoter CpG island was 76.7% (23/30) in the tumor tissues and 63.3% (19/30) in serum of gastric cancer patients, and the difference had no statistical significance. Conclusion: Our studies suggest that ERCC1 gene promoter CpG island methylation can be detected in a high proportion of the serum consisting with that in tumor tissues of gastric cancer patients, and the detection of methylation status of ERCC1 gene in peripheral blood provides a more simple, fast and reliable way for the medical treatment of gastric cancer and also provides the possible theoretical basis for the CpG island methylation of ERCC1 gene promoter as a target for the treatment of gastric cancer.

Key words: Gastric cancer, ERCC1 gene, CpG island, Methylation, Methylation specific PCR