Analysis of correlation between the important Helicobacter pylori virulence genes (CagA, SabA and Oip) and gastric epithelial stem cells (LGR5) in patients with gastric disease

Safyia Abdullah, Wasan A. Bakir, Mais Alsikafi
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Abstract

Background: Gastric diseases are commonly caused by Helicobacter pylori, by colonizing the mucosa of the gastric epithelium in more than half of the population worldwide. It has the ability for adhering to gastric epithelium, with an important aspect of the pathogenicity of the microorganism facilitating the transport of certain proteins such as CagA, sialic acid-binding adhesion (SabA), and outer inflammatory protein (Oip) into that epithelium. The LGR5 are markers that were recognized as cancer stem cells marker that have prognostic value in some disorders such as gastric cancers (GCs), metaplasia, and inflammation of gastric mucosa. This study aimed for determining the association between expression of LGR5 in patients with gastric diseases and the presence of some virulence genes (CagA, SabA and Oip). Patients, Material and Methods: For the 140 patients enrolled H. pylori virulence factors including (CagA, SabA and Oip) was detected using Multiplex real-time polymerase chain reaction, while LGR5 expressions were carried out via immunohistochemistry. Results: SabA and Oip was significant difference with gastric disease such as GC, gastric metaplasia and gastritis with and without H. pylori. While no significant difference Cag gene with gastric disease due to all patient have Cag gene. LGR5 stem cell marker expression has significant difference with GC and gastric metaplasia. Conclusion: There was a significant increase in H. pylori Ag (SabA and Oip) expression among patients with gastric disease compared to the apparently normal individuals this might be able to be that H. pylori as one of the risk factor for developing cancer. However, no significant between H. pylori Cag Ag expression among patients with gastric disease due to all the patients infected with H. pylori has Cag gene (100%). It is suggested that LGR5 may play an important role in gastric carcinoma formation and may be used as a potential marker for the progression in patients with gastric disease.
胃癌患者幽门螺杆菌重要毒力基因CagA、SabA和Oip与胃上皮干细胞(LGR5)的相关性分析
背景:胃疾病通常是由幽门螺杆菌引起的,幽门螺杆菌在全球一半以上的人群中定植于胃上皮粘膜。它具有粘附于胃上皮的能力,微生物致病性的一个重要方面促进了某些蛋白质的转运,如CagA、唾液酸结合粘附(SabA)和外部炎症蛋白(Oip)进入该上皮。LGR5是被识别为癌症干细胞标志物的标志物,其在某些疾病中具有预后价值,如胃癌(GC)、化生和胃粘膜炎症。本研究旨在确定胃疾病患者中LGR5的表达与某些毒力基因(CagA、SabA和Oip)的存在之间的关系。患者、材料和方法:对140名入选的幽门螺杆菌患者,采用多重实时聚合酶链反应检测毒力因子(CagA、SabA和Oip),同时通过免疫组织化学检测LGR5的表达。结果:SabA和Oip与胃癌、胃化生和胃炎伴幽门螺杆菌和不伴幽门螺杆杆菌有显著性差异。Cag基因与胃癌无显著性差异,因为所有患者均具有Cag基因。LGR5干细胞标志物的表达与胃癌和胃化生有显著差异。结论:与表面正常人相比,胃病患者幽门螺杆菌Ag(SabA和Oip)的表达显著增加,这可能是幽门螺杆菌成为癌症发生的危险因素之一。然而,由于所有感染幽门螺杆菌的患者都具有Cag基因,幽门螺杆菌Cag-Ag在胃癌患者中的表达没有显著差异(100%)。提示LGR5可能在胃癌的形成中发挥重要作用,并可作为胃癌患者进展的潜在标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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