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dc.creatorGholizadeh, M. (Maryam)-
dc.creatorSzelag-Pieniek, S. (Sylwia)-
dc.creatorPost, M. (Mariola)-
dc.creatorKurzawski, M. (Mateusz)-
dc.creatorPrieto, J. (Jesús)-
dc.creatorArgemí, J. (Josepmaria)-
dc.creatorDrozdzik, M. (Marek)-
dc.creatorKaderali, L. (Lars)-
dc.identifier.citationGholizadeh, M. (Maryam); Szelag-Pieniek, S. (Sylwia); Post, M. (Mariola); et al. "Identifying Differentially Expressed MicroRNAs, Target Genes, and Key Pathways Deregulated in Patients with Liver Diseases". International Journal of Molecular Sciences. 21 (19), 2020, 7368es_ES
dc.description.abstractLiver diseases are important causes of morbidity and mortality worldwide. The aim of this study was to identify differentially expressed microRNAs (miRNAs), target genes, and key pathways as innovative diagnostic biomarkers in liver patients with different pathology and functional state. We determined, using RT-qPCR, the expression of 472 miRNAs in 125 explanted livers from subjects with six different liver pathologies and from control livers. ANOVA was employed to obtain differentially expressed miRNAs (DEMs), and miRDB (MicroRNA target prediction database) was used to predict target genes. A miRNA–gene differential regulatory (MGDR) network was constructed for each condition. Key miRNAs were detected using topological analysis. Enrichment analysis for DEMs was performed using the Database for Annotation, Visualization, and Integrated Discovery (DAVID). We identified important DEMs common and specific to the different patient groups and disease progression stages. hsa-miR-1275 was universally downregulated regardless the disease etiology and stage, while hsa-let-7a*, hsa-miR-195, hsa-miR-374, and hsa-miR-378 were deregulated. The most significantly enriched pathways of target genes controlled by these miRNAs comprise p53 tumor suppressor protein (TP53)-regulated metabolic genes, and those involved in regulation of methyl-CpG-binding protein 2 (MECP2) expression, phosphatase and tensin homolog (PTEN) messenger RNA (mRNA) translation and copper homeostasis. Our findings show a novel panel of deregulated miRNAs in the liver tissue from patients with different liver pathologies. These miRNAs hold potential as biomarkers for diagnosis and staging of liver diseases.es_ES
dc.description.sponsorshipThis study was funded by grants from the National Science Center, Cracow, Poland, grant number UMO-2015/18/M/NZ7/000410, and the German Ministry for Education and Research (BMBF), grant number 031L0032 (LiSyM).es_ES
dc.subjectLiver diseasees_ES
dc.subjectRegulatory networkses_ES
dc.titleIdentifying Differentially Expressed MicroRNAs, Target Genes, and Key Pathways Deregulated in Patients with Liver Diseaseses_ES
dc.description.noteThis article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dadun.citation.publicationNameInternational Journal of Molecular Scienceses_ES

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