Overexpression of miR-146a and miR-155 are Potentially Biomarkers and Predict Unfavorable Relationship between Gastric Cancer and Helicobacter pylori Infection.

Chonnam medical journal Pub Date : 2023-09-01 Epub Date: 2023-09-25 DOI:10.4068/cmj.2023.59.3.167
Masoud Karimi, Abdolreza Mohammadnia, Mohammad Amin Amini, Azar Ghavimi Shamekh, Elahe Derakhshanfar, Farzaneh Hosseini
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Abstract

Gastric Cancer (GC) is one of the most dangerous malignancies in the world. This study aims to evaluate the relationship between miR-146a and miR-155 in patients with H. pylori infections with GC compared to H. pylori-infected patients and healthy subjects. Forty patients with H. pylori and GC positive diagnoses and 40 patients with H. pylori positive and GC negative diagnoses, and 40 healthy persons were selected. The expression of miR-146a and miR-155 genes in the whole blood was examined using qRT-PCR. Moreover, ROC curves were drawn to represent the sensitivity and specificity of miR-146a and miR-155 expression as biomarkers. The results showed the expression of miR-146a and miR-155 in the whole blood of patients with H. pylori and GC positive diagnoses are significantly higher than in healthy individuals and are non-significantly enhanced compared to H. pylori positive and GC negative. Also, the results stated miR-146a and miR-155 expression in the whole blood of patients who are H. pylori positive and GC negative are significantly increased compared to healthy individuals. Furthermore, the ROC curve analysis of miR-146a and miR-155 RNA level demonstrated the two miRNAs have an appropriate sensitivity and specificity for diagnostic goals. In conclusion, H. pylori infection may increase the expression of miR-146a and miR-155 in patients with H. pylori and GC positive diagnoses, which can be effective in the curbing the progression of GC. For this reason, up-regulation of miR-146a and miR-155 along with H. pylori infection might contribute to the pathogenesis of GC, and also can be suggested as biomarkers for GC diagnosis and treatment.

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miR-146a和miR-155的过度表达是潜在的生物标志物,可预测癌症与幽门螺杆菌感染之间的不利关系。
癌症是世界上最危险的恶性肿瘤之一。本研究旨在评估胃癌幽门螺杆菌感染患者的miR-146a和miR-155与幽门螺杆菌患者和健康受试者的关系。选择40名幽门螺杆菌和GC阳性诊断的患者、40名幽门螺旋菌阳性和GC阴性诊断的患者以及40名健康人。使用qRT-PCR检测全血中miR-146a和miR-155基因的表达。此外,绘制ROC曲线以表示miR-146a和miR-155表达作为生物标志物的敏感性和特异性。结果显示,在幽门螺杆菌和GC阳性诊断的患者的全血中,miR-146a和miR-155的表达显著高于健康个体,并且与幽门螺杆菌阳性和GC阴性相比没有显著增强。此外,研究结果表明,与健康个体相比,幽门螺杆菌阳性和GC阴性患者全血中miR-146a和miR-155的表达显著增加。此外,miR-146a和miR-155RNA水平的ROC曲线分析表明,这两种miRNA对诊断目标具有适当的敏感性和特异性。总之,在幽门螺杆菌和GC阳性诊断的患者中,幽门螺杆菌感染可能会增加miR-146a和miR-155的表达,这可以有效地抑制GC的进展。因此,miR-146a和miR-155的上调以及幽门螺杆菌感染可能有助于GC的发病机制,也可以作为GC诊断和治疗的生物标志物。
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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