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首页> 外文期刊>BMC Gastroenterology >The overmethylated genes in Helicobacter pylori-infected gastric mucosa are demethylated in gastric cancers
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The overmethylated genes in Helicobacter pylori-infected gastric mucosa are demethylated in gastric cancers

机译:幽门螺杆菌感染的胃黏膜中甲基化过高的基因在胃癌中脱甲基

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Background The transitional-CpG sites between weakly methylated genes and densely methylated retroelements are overmethylated in the gastric mucosa infected with Helicobacter pylori (H. pylori) and they are undermethylated in the gastric cancers depending on the level of loss of heterozygosity (LOH) events. This study delineated the transitional-CpG methylation patterns of CpG-island-containing and -lacking genes in view of the retroelements. Methods The transitional-CpG sites of eight CpG-island-containing genes and six CpG-island-lacking genes were semi-quantitatively examined by performing radioisotope-labelling methylation-specific PCR under stringent conditions. The level of LOH in the gastric cancers was estimated using the 40 microsatellite markers on eight cancer-associated chromosomes. Each gene was scored as overmethylated or undermethylated based on an intermediate level of transitional-CpG methylation common in the H. pylori-negative gastric mucosa. Results The eight CpG-island genes examined were overmethylated depending on the proximity to the nearest retroelement in the H. pylori-positive gastric mucosa. The six CpG-island-lacking genes were similarly methylated in the H. pylori-positive and -negative gastric mucosa. In the gastric cancers, long transitional-CpG segments of the CpG-island genes distant from the retroelements remained overmethylated, whereas the overmethylation of short transitional-CpG segments close to the retroelements was not significant. Both the CpG-island-containing and -lacking genes tended to be decreasingly methylated in a LOH-level-dependent manner. Conclusions The overmethylated genes under the influence of retroelement methylation in the H. pylori-infected stomach are demethylated in the gastric cancers influenced by LOH.
机译:背景技术弱甲基化基因和密集甲基化逆转录元件之间的CpG过渡位点在感染幽门螺杆菌(H. pylori)的胃粘膜中被甲基化程度过高,而在胃癌中根据杂合度丧失(LOH)事件的程度被甲基化程度低下。这项研究从后元素的角度描绘了含CpG岛和缺失岛基因的过渡CpG甲基化模式。方法在严格的条件下,通过放射性同位素标记甲基化特异性PCR,半定量检测了八个含CpG岛的基因和六个CpG岛缺失的基因的过渡CpG位点。使用八个与癌症相关的染色体上的40个微卫星标记来估计胃癌中LOH的水平。根据幽门螺杆菌阴性胃黏膜常见的过渡CpG甲基化的中间水平,将每个基因的甲基化程度都记为过甲基化或甲基化程度不足。结果根据幽门螺杆菌阳性胃粘膜中最接近的逆向元件的接近程度,检测的八个CpG-岛基因被甲基化。在幽门螺杆菌阳性和阴性胃粘膜中,六个缺乏CpG的基因被甲基化。在胃癌中,远离逆转录元件的CpG-岛基因的长过渡CpG片段保持甲基化,而靠近逆转录元件的短过渡CpG片段的超甲基化作用不明显。含有CpG岛的基因和缺乏CpG的基因都倾向于以依赖LOH水平的方式降低甲基化。结论在幽门螺杆菌感染的胃癌中,在幽门螺杆菌感染的胃中受逆向甲基化影响的过甲基化基因被去甲基化。

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