Analysis of Gene Expression Omnibus high-throughput sequencing data for the determination of microribonucleic acids in the blood plasma of patients with glioblastomas

A. Pushkin, D. Gvaldin, N. Timoshkina, E. Rostorguev, L. Vladimirova, E. A. Dzenkova
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引用次数: 1

Abstract

Purpose of the study. This work is devoted to the study of blood plasma miRNA patterns in blood plasma using high-throughput sequencing of the Omnibus Gene Expression base and the search for candidate miRNA molecules for the development of a minimally invasive diagnostic panel.Materials and methods. Basing on the open dataset of Omnibus Expression of the NCBI GSE150956 Gene, groups of samples with glioblastoma and conventionally healthy donors were formed. For each sample, information on the levels of miRNA expression was extracted. Determination of significant miRNAs using machine learning algorithms of the R 4.0.4 project. For significant miRNAs, target genes have been performed, an analysis of the improvement of functional characteristics and interactome analysis of target genes of miRNA were performed.Results. The study analyzed the data of 131 samples, where 35 samples with glioblastoma and 96 samples of the conditionally healthy group. Differential expression data were obtained for 945 miRNA. Two panels were obtained using machine learning methods, common miRNA – hsa-miR 3180, hsa-miR 3180-3p, hsa-miR 6782-5p, hsa-miR 182-5p, hsa-miR 133b and hsa-miR 670-3p. For significant miRNAs, information was obtained on experimentally confirmed target genes, a gene ontology demonstrating their participation in enzyme binding, participation in the regulation of primary cellular metabolic processes, and the development of glioblastomas and cancer in general.Conclusion. As a result of layer-by-layer filtering and application of machine learning algorithms, significant miRNAs were identified that are candidates for a diagnostic panel of a minimally invasive method of high-grade glial tumors.
胶质母细胞瘤患者血浆中微核糖核酸的基因表达分析
研究目的:这项工作致力于利用Omnibus基因表达基的高通量测序研究血浆中的血浆miRNA模式,并寻找候选miRNA分子以开发微创诊断板。材料和方法。以NCBI GSE150956基因Omnibus Expression开放数据集为基础,将胶质母细胞瘤和常规健康供体样本分组。对于每个样本,提取miRNA表达水平的信息。使用R 4.0.4项目的机器学习算法确定重要的mirna。对重要的miRNA进行了靶基因分析,对miRNA靶基因的功能特征改进进行了分析,并进行了相互作用组分析。该研究分析了131个样本的数据,其中35个样本患有胶质母细胞瘤,96个样本属于条件健康组。获得945个miRNA的差异表达数据。使用机器学习方法获得两个面板,常见miRNA - hsa-miR 3180, hsa-miR 3180-3p, hsa-miR 6782-5p, hsa-miR 182-5p, hsa-miR 133b和hsa-miR 670-3p。对于重要的mirna,获得了实验证实的靶基因的信息,基因本体表明它们参与酶结合,参与初级细胞代谢过程的调节,以及胶质母细胞瘤和癌症的发展。由于逐层过滤和机器学习算法的应用,确定了重要的mirna,这些mirna是微创方法诊断高级别胶质细胞肿瘤的候选物。
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