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脑胶质瘤中ppENK基因启动子区的甲基化状态研究

吴开福 徐培坤 朱立新 赵庭生 刘正

国际神经病学神经外科学杂志2011,Vol.38Issue(6):520-524,5.
国际神经病学神经外科学杂志2011,Vol.38Issue(6):520-524,5.

脑胶质瘤中ppENK基因启动子区的甲基化状态研究

Methylation status of promoter of mismatch repair gene ppENK in glioma

吴开福 1徐培坤 1朱立新 2赵庭生 1刘正1

作者信息

  • 1. 安徽医科大学第一附属医院神经外科,安徽 合肥 230022
  • 2. 安徽医科大学第一附属医院中心实验室,安徽 合肥 230022
  • 折叠

摘要

Abstract

Objective To explore the methylation status of ppENK promoter region in glioma and discuss the abnormal ppENK gene promoter methylation gliomas occurrence and development, the relationship between role and clinical pathological material. Methods Methylation status of the ppENK promoter region was assayed in 32 glioma tissues and 10 normal brain tissues by nested polymerase chain reaction (nPCR) and Bisulfite sequence polymerase chain reaction (BSP). Results BSP showed that the ppENK promoter region was hypermethylated in 13 of the 32 glioma tissues and no methylation of ppENK promoter was detected in the 10 normal brain tissues. The promoter hypermethylation ratio of ppENK gene in glioma tissues (40.6% ) was significantly higher than that in normal brain tissues (0%, P=0.015). Moreover, we found that the aberrant promoter methylation of ppENK gene was significantly correlated with tumor grade ( P = 0.006) , but not correlated with age, sex and tumor types of patients (P=0.154, 0.961 and 0.694, respectively). The rate (21. 1% ) of ppENK promoter methylation in grades I ~ II gliomas was significantly lower than that (69. 2% ) in grades M ~ IV gliomas (P <0.05). Conclusions ppENK. Promoter ( CpG island) hypermethylation exists in glioma, which may correlates with the occurrence of glioma. The expression and promoter region methylation of ppENK gene in the gliomas are related to pathological grades, not related to the patients age, gender and tumor size factors.

关键词

ppENK/甲基化/胶质瘤

Key words

ppENK/ Methylation/ glioma

引用本文复制引用

吴开福,徐培坤,朱立新,赵庭生,刘正..脑胶质瘤中ppENK基因启动子区的甲基化状态研究[J].国际神经病学神经外科学杂志,2011,38(6):520-524,5.

基金项目

安徽省卫生厅基金(2010B013) (2010B013)

国际神经病学神经外科学杂志

OACSTPCD

1673-2642

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