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LINE-1低甲基化与幽门螺杆菌相关性皱襞增生性胃炎中CpG岛甲基化增加有关。

LINE-1 hypomethylation is associated with increased CpG island methylation in Helicobacter pylori-related enlarged-fold gastritis.

作者信息

Yamamoto Eiichiro, Toyota Minoru, Suzuki Hiromu, Kondo Yutaka, Sanomura Tamana, Murayama Yoko, Ohe-Toyota Mutsumi, Maruyama Reo, Nojima Masanori, Ashida Masami, Fujii Kyoko, Sasaki Yasushi, Hayashi Norio, Mori Mitsuru, Imai Kohzoh, Tokino Takashi, Shinomura Yasuhisa

机构信息

First Department of Internal Medicine, Sapporo Medical University, South 1,West 16, Chuo-ku, Sapporo 060-8543, Japan.

出版信息

Cancer Epidemiol Biomarkers Prev. 2008 Oct;17(10):2555-64. doi: 10.1158/1055-9965.EPI-08-0112.

Abstract

BACKGROUND

The molecular mechanism by which Helicobacter pylori infection leads to gastric cancer is not fully understood. Similarly, patients with enlarged-fold (EF+) gastritis, one cause of which is H. pylori infection, have an increased risk for gastric cancer, although again molecular mechanism is unclear. In the present study, we analyzed the methylation status of long interspersed nucleotide elements (LINE-1) and three cancer-related genes in a panel of gastric mucosae, with or without EF+ gastritis.

METHODS

We used bisulfite pyrosequencing to assess the levels of LINE-1, CDH1, CDH13, and PGP9.5 methylation in 78 gastric mucosa specimens from 48 patients.

RESULTS

Levels of LINE-1 methylation were significantly reduced in mucosae from patients with EF+ gastritis. This hypomethylation of LINE-1 was associated with increased methylation of the 5' CpG islands of the genes, which suggests that, in EF+ gastritis, the methylation of the promoter regions of certain genes is accompanied by global demethylation of repetitive sequences.

CONCLUSIONS

Our results indicate that genomewide hypomethylation and regional hypermethylation occur in EF+ gastritis and may contribute to the tumorigenesis of diffuse-type gastric cancers.

摘要

背景

幽门螺杆菌感染导致胃癌的分子机制尚未完全明确。同样,皱襞增大型(EF+)胃炎患者患胃癌的风险增加,幽门螺杆菌感染是其病因之一,不过分子机制同样不明。在本研究中,我们分析了一组有或无EF+胃炎的胃黏膜中长散在核苷酸元件(LINE-1)及三个癌症相关基因的甲基化状态。

方法

我们采用亚硫酸氢盐焦磷酸测序法评估了48例患者的78份胃黏膜标本中LINE-1、CDH1、CDH13和PGP9.5的甲基化水平。

结果

EF+胃炎患者胃黏膜中LINE-1甲基化水平显著降低。LINE-1的这种低甲基化与基因5' CpG岛甲基化增加相关,这表明在EF+胃炎中,某些基因启动子区域的甲基化伴随着重复序列的全基因组去甲基化。

结论

我们的结果表明,EF+胃炎中发生全基因组低甲基化和区域高甲基化,可能促进弥漫型胃癌的肿瘤发生。

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