Leung Wai K, Man Ellen P S, Yu Jun, Go Minnie Y Y, To Ka-fai, Yamaoka Yoshio, Cheng Victoria Y Y, Ng Enders K W, Sung Joseph J Y
Institute of Digestive Disease, Faculty of Medicine, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong.
Clin Cancer Res. 2006 May 15;12(10):3216-21. doi: 10.1158/1078-0432.CCR-05-2442.
Promoter hypermethylation of E-cadherin plays an important role on gastric cancer development. Whereas E-cadherin methylation was frequently detected in the stomach of Helicobacter pylori-infected individuals, we tested whether eradication of H. pylori alters the methylation status of the noncancerous gastric epithelium.
Endoscopic biopsies were taken from the antrum and corpus of H. pylori-infected subjects without gastric cancer. Presence of methylated E-cadherin sequences in the gastric specimens was detected by methylation-specific PCR. Bisulfite DNA sequencing was done to determine the topographical distribution and changes in methylation profiles with H. pylori eradication.
Among the 28 H. pylori-infected subjects (median age, 44.5 years), 15 (53.6%) had E-cadherin methylation detected in stomach at baseline. Discordant methylation patterns between the antrum and corpus were noted in six patients. One year after successful H. pylori eradication, there was a significant reduction in the methylation density of the promoter region and exon 1 of the E-cadherin gene as detected by bisulfite DNA sequencing (P < 0.001).
Promoter methylation in E-cadherin was frequently detected in the stomach of H. pylori-infected individuals. Eradication of H. pylori might possibly reduce the methylation density in E-cadherin gene and the chance of subsequent neoplastic transformation.
E-钙黏蛋白启动子高甲基化在胃癌发生中起重要作用。鉴于在幽门螺杆菌感染个体的胃中经常检测到E-钙黏蛋白甲基化,我们测试了根除幽门螺杆菌是否会改变非癌性胃上皮的甲基化状态。
从无胃癌的幽门螺杆菌感染受试者的胃窦和胃体取内镜活检组织。通过甲基化特异性PCR检测胃标本中甲基化E-钙黏蛋白序列的存在。进行亚硫酸氢盐DNA测序以确定幽门螺杆菌根除后甲基化谱的拓扑分布和变化。
在28名幽门螺杆菌感染受试者(中位年龄44.5岁)中,15名(53.6%)在基线时胃中检测到E-钙黏蛋白甲基化。6名患者胃窦和胃体之间的甲基化模式不一致。成功根除幽门螺杆菌一年后,通过亚硫酸氢盐DNA测序检测到E-钙黏蛋白基因启动子区域和外显子1的甲基化密度显著降低(P<0.001)。
在幽门螺杆菌感染个体的胃中经常检测到E-钙黏蛋白启动子甲基化。根除幽门螺杆菌可能会降低E-钙黏蛋白基因的甲基化密度以及随后发生肿瘤转化的机会。