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首页> 外文期刊>Nature Communications >Epigenetic silencing of miR-210 increases the proliferation of gastric epithelium during chronic Helicobacter pylori infection
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Epigenetic silencing of miR-210 increases the proliferation of gastric epithelium during chronic Helicobacter pylori infection

机译: miR-210 的表观遗传沉默增加了慢性幽门螺杆菌感染期间胃上皮细胞的增殖

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Persistent colonization of the gastric mucosa by Helicobacter pylori (Hp) elicits chronic inflammation and aberrant epithelial cell proliferation, which increases the risk of gastric cancer. Here we examine the ability of microRNAs to modulate gastric cell proliferation in response to persistent Hp infection and find that epigenetic silencing of miR-210 plays a key role in gastric disease progression. Importantly, DNA methylation of the miR-210 gene is increased in Hp-positive human gastric biopsies as compared with Hp-negative controls. Moreover, silencing of miR-210 in gastric epithelial cells promotes proliferation. We identify STMN1 and DIMT1 as miR-210 target genes and demonstrate that inhibition of miR-210 expression augments cell proliferation by activating STMN1 and DIMT1 . Together, our results highlight inflammation-induced epigenetic silencing of miR-210 as a mechanism of induction of chronic gastric diseases, including cancer, during Hp infection.
机译:幽门螺杆菌(Hp)持续在胃粘膜上定殖会引起慢性炎症和上皮细胞异常增殖,从而增加患胃癌的风险。在这里,我们检查了microRNA调节Hp持续感染引起的胃细胞增殖的能力,并发现miR-210的表观遗传沉默在胃病进展中起关键作用。重要的是,与Hp阴性对照相比,在Hp阳性的人胃活检中miR-210基因的DNA甲基化增加。此外,使胃上皮细胞中的miR-210沉默会促进增殖。我们确定STMN1和DIMT1为miR-210靶基因,并证明抑制miR-210的表达通过激活STMN1和DIMT1增强细胞增殖。在一起,我们的结果强调了炎症诱导的miR-210的表观遗传沉默是Hp感染期间诱导慢性胃病(包括癌症)的一种机制。

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