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http://hdl.handle.net/11452/29535
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DC Field | Value | Language |
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dc.date.accessioned | 2022-11-22T10:21:05Z | - |
dc.date.available | 2022-11-22T10:21:05Z | - |
dc.date.issued | 2016-07-31 | - |
dc.identifier.citation | Budak, F. vd. (2016). "Altered expressions of miR-1238-3p, miR-494, miR-6069, and miR-139-3p in the formation of chronic Brucellosis". Journal of Immunology Research, 2016, 1-11. | en_US |
dc.identifier.issn | 2314-8861 | - |
dc.identifier.issn | 2314-7156 | - |
dc.identifier.uri | https://doi.org/10.1155/2016/4591468 | - |
dc.identifier.uri | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046029/ | - |
dc.identifier.uri | http://hdl.handle.net/11452/29535 | - |
dc.description.abstract | Brucellosis is a zoonotic disease that is still endemic in developing countries. Despite early diagnosis and treatment of patients, chronic infections are seen in 10-30% of patients. In this study, we aimed to investigate the immunological factors that play roles in the transition of brucellosis from acute infection into chronic infection. Here, more than 2000 miRNAs were screened in peripheral blood mononuclear cells (PBMCs) of patients with acute or chronic brucellosis and healthy controls by using miRNA array, and the results of the miRNA array were validated through qRT-PCR. Findings were evaluated using GeneSpring GX (Agilent) 13.0 software and KEGG pathway analysis. Four miRNAs were expressed in the chronic group but were not expressed in acute and control groups. Among these miRNAs, the expression level of miR-1238-3p was increased while miR-494, miR-6069, and miR-1393p were decreased (p< 0.05, fold change > 2). These miRNAs have the potential to be markers for chronic cases. The differentially expressed miRNAs and their predicted target genes involved in endocytosis, regulation of actin cytoskeleton, MAPK signaling pathway, and cytokine-cytokine receptor interaction and its chemokine signaling pathway indicate their potential roles in chronic brucellosis and its progression. It is the first study of miRNA expression analysis of human PBMC to clarify the mechanism of inveteracy in brucellosis. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Hindawi | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Immunology | en_US |
dc.subject | Dendritic cell maturation | en_US |
dc.subject | B-virus infection | en_US |
dc.subject | Microrna expression | en_US |
dc.subject | Gene-expression | en_US |
dc.subject | Up-regulation | en_US |
dc.subject | Integrated analysis | en_US |
dc.subject | Abortus invasion | en_US |
dc.subject | Down-regulation | en_US |
dc.subject | Cancer cells | en_US |
dc.subject | TNF-alpha | en_US |
dc.subject.mesh | Acute disease | en_US |
dc.subject.mesh | Biomarkers | en_US |
dc.subject.mesh | Brucellosis | en_US |
dc.subject.mesh | Chronic disease | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Gene expression profiling | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Metabolic networks and pathways | en_US |
dc.subject.mesh | MicroRNAs | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Real-time polymerase chain reaction | en_US |
dc.title | Altered expressions of miR-1238-3p, miR-494, miR-6069, and miR-139-3p in the formation of chronic Brucellosis | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000385116100001 | tr_TR |
dc.identifier.scopus | 2-s2.0-84990876577 | tr_TR |
dc.relation.tubitak | SBAG-111S183 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/İmmünoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Klinik Mikrobiyoloji ve Enfeksiyon Hastalıkları Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Mikrobiyoloji Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0003-0463-6818 | tr_TR |
dc.contributor.orcid | 0000-0002-5956-8755 | tr_TR |
dc.identifier.startpage | 1 | tr_TR |
dc.identifier.endpage | 11 | tr_TR |
dc.identifier.volume | 2016 | tr_TR |
dc.relation.journal | Journal of Immunology Research | en_US |
dc.contributor.buuauthor | Budak, Ferah | - |
dc.contributor.buuauthor | Bal, Salih Haldun | - |
dc.contributor.buuauthor | Tezcan, Gülçin | - |
dc.contributor.buuauthor | Akalın, Halis | - |
dc.contributor.buuauthor | Göral, Güher | - |
dc.contributor.buuauthor | Oral, Haluk Barbaros | - |
dc.contributor.researcherid | K-7285-2012 | tr_TR |
dc.contributor.researcherid | AAU-8952-2020 | tr_TR |
dc.contributor.researcherid | F-4657-2014 | tr_TR |
dc.contributor.researcherid | F-8554-2017 | tr_TR |
dc.contributor.researcherid | AAH-3843-2020 | tr_TR |
dc.identifier.pubmed | 27722176 | tr_TR |
dc.subject.wos | Immunology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q2 | en_US |
dc.contributor.scopusid | 6701913697 | tr_TR |
dc.contributor.scopusid | 57191480128 | tr_TR |
dc.contributor.scopusid | 25650627600 | tr_TR |
dc.contributor.scopusid | 57207553671 | tr_TR |
dc.contributor.scopusid | 6603453166 | tr_TR |
dc.contributor.scopusid | 7004498001 | tr_TR |
dc.subject.scopus | Animals; Zoonosis; Bovine Brucellosis | en_US |
dc.subject.emtree | Cytokine | en_US |
dc.subject.emtree | Doxycycline | en_US |
dc.subject.emtree | MicroRNA | en_US |
dc.subject.emtree | Microrna 1238 3p | en_US |
dc.subject.emtree | Microrna 139 3p | en_US |
dc.subject.emtree | Microrna 1914 3p | en_US |
dc.subject.emtree | Microrna 22 5p | en_US |
dc.subject.emtree | Microrna 335 5p | en_US |
dc.subject.emtree | Microrna 339 5p | en_US |
dc.subject.emtree | Microrna 494 | en_US |
dc.subject.emtree | Microrna 575 | en_US |
dc.subject.emtree | Microrna 6069 | en_US |
dc.subject.emtree | Mitogen activated protein kinase | en_US |
dc.subject.emtree | Rifampicin | en_US |
dc.subject.emtree | Unclassified drug | en_US |
dc.subject.emtree | Biological marker | en_US |
dc.subject.emtree | MIRN1238 microRNA, human | en_US |
dc.subject.emtree | MIRN139 microRNA, human | en_US |
dc.subject.emtree | MIRN494 microRNA, human | en_US |
dc.subject.emtree | Actin filament | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Brucellosis | en_US |
dc.subject.emtree | Chronic brucellosis | en_US |
dc.subject.emtree | Chronicity | en_US |
dc.subject.emtree | Clinical article | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Disease course | en_US |
dc.subject.emtree | Endocytosis | en_US |
dc.subject.emtree | Fatigue | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Gene expression | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Human cell | en_US |
dc.subject.emtree | Immune response | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Peripheral blood mononuclear cell | en_US |
dc.subject.emtree | Protein protein interaction | en_US |
dc.subject.emtree | Reverse transcription polymerase chain reaction | en_US |
dc.subject.emtree | Signal transduction | en_US |
dc.subject.emtree | Acute disease | en_US |
dc.subject.emtree | Blood | en_US |
dc.subject.emtree | Brucellosis | en_US |
dc.subject.emtree | Chronic disease | en_US |
dc.subject.emtree | Gene expression profiling | en_US |
dc.subject.emtree | Genetics | en_US |
dc.subject.emtree | Immunology | en_US |
dc.subject.emtree | Metabolism | en_US |
dc.subject.emtree | Microbiology | en_US |
dc.subject.emtree | Middle aged | en_US |
dc.subject.emtree | Real time polymerase chain reaction | en_US |
Appears in Collections: | Scopus Web of Science |
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