揭示 IFIT3 基因和免疫代谢途径在银屑病中的作用:诊断标记和治疗靶点的生物信息学探索。

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Frontiers in Molecular Biosciences Pub Date : 2024-08-22 eCollection Date: 2024-01-01 DOI:10.3389/fmolb.2024.1439837
Guangshan Chen, Xi Chen, Xingwu Duan, Runtian Zhang, Chunxiao Bai
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引用次数: 0

摘要

背景:通过生物信息学方法探讨IFIT3基因在银屑病患者皮损中的功能及相关信号通路,以确定银屑病潜在的特异性分子标记:方法:使用 "limma "R软件包分析基因表达总库中的三个数据集(GSE13355、GSE30999和GSE106992),筛选差异基因。利用 STRING 数据库进行了基因本体(GO)富集分析、京都基因和基因组百科全书(KEGG)通路富集分析以及蛋白质-蛋白质相互作用网络整合。然后,利用 Metascape 数据库通过基因组富集分析(GSEA)提取并分析了 IFIT3 子网络,以验证基因分化和疾病组织鉴定的有效性:结果:本研究共获得426个差异基因,其中322个基因显著上调,104个基因显著下调。GO富集分析显示,差异基因主要涉及免疫和代谢;KEGG通路富集分析主要包括趋化因子信号通路、PPAR信号通路和IL-17信号通路等。基于 IFIT3 子网络分析发现,IFIT3 主要参与病毒、细菌和其他微生物的生物学过程。通过GSEA获得的通路主要与免疫、新陈代谢和抗病毒活性有关。IFIT3在银屑病皮损中高表达,因此可能有助于银屑病的诊断:结论:通过生物信息学分析获得了银屑病的差异基因、生物过程和信号通路,尤其是与 IFIT3 基因相关的信息和诊断效率。这些结果有望为探索银屑病的发病机制提供理论依据和新的研究方向,并有助于寻找诊断标志物和开发药物治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unraveling the roles of IFIT3 gene and immune-metabolic pathways in psoriasis: a bioinformatics exploration for diagnostic markers and therapeutic targets.

Background: The functions and related signal pathways of the IFIT3 gene in the skin lesions of patients with psoriasis were explored through bioinformatics methods to determine the potential specific molecular markers of psoriasis.

Methods: The "limma" R package was used to analyze three datasets from the Gene Expression Omnibus database (GSE13355, GSE30999 and GSE106992), and the differential genes were screened. The STRING database was used for gene ontology (GO) enrichment analysis, Kyoto encyclopedia of genes and genomes (KEGG) pathway enrichment analysis, and protein-protein interaction network integration. Then, the IFIT3 subnetwork was extracted and analyzed by gene set enrichment analysis (GSEA) using the Metascape database to verify the effectiveness of gene differentiation and disease tissue identification.

Results: In this study, 426 differential genes were obtained, of which 322 were significantly upregulated and 104 were significantly downregulated. GO enrichment analysis showed that the differential genes were mainly involved in immunity and metabolism; the KEGG pathway enrichment analysis mainly included the chemokine signal pathway, PPAR signal pathway, and IL-17 signal pathway, among others. Based on the IFIT3 subnetwork analysis, it was found that IFIT3 was mainly involved in the biological processes of viruses, bacteria, and other microorganisms. The pathways obtained by GSEA were mainly related to immunity, metabolism, and antiviral activities. IFIT3 was highly expressed in psoriatic lesions and may thus be helpful in the diagnosis of psoriasis.

Conclusion: The differential genes, biological processes, and signal pathways of psoriasis, especially information related to and diagnostic efficiency of the IFIT3 gene, were obtained by bioinformatics analysis. These results are expected to provide the theoretical basis and new directions for exploring the pathogenesis of psoriasis, in addition to helping with finding diagnostic markers and developing drug treatment targets.

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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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