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dc.creatorKourti M., Sokratous M., Katsiari C.G.en
dc.date.accessioned2023-01-31T08:45:43Z
dc.date.available2023-01-31T08:45:43Z
dc.date.issued2020
dc.identifier10.31138/MJR.31.1.71
dc.identifier.issn24593516
dc.identifier.urihttp://hdl.handle.net/11615/75344
dc.description.abstractmiRNAs are small non-coding RNA molecules that participate through silencing in post-transcriptional regulation of gene expression. Recent studies have highlighted the importance of microRNAs (miRNAs) as regulators of both the innate and the adaptive immune response. There are emerging data regarding the role of miRNAs in patients with Systemic Lupus Erythematosus (SLE). One of the main stimuli for the induction of miR-21 is hypoxia. Moreover, the expression and function of miR-210 is directly related to the activity of "hypoxia inducible factor-1a" (HIF-1a). The aim of the study is to examine the regulation of miR-21 and mir-210 in patients with SLE based on the hypothesis that cellular hypoxia may have an important role in SLE pathogenesis. Plasma, PBMC and urine samples will be collected from patients with SLE and normal controls. miR expression will be studied with real-time PCR. Functional experiments will examine the effect of miR-21 and miR-210 on HIFa and ERK1/2 και PI3K/AKT signalling pathways. The study will provide novel data regarding the expression and the role of miR-21 and miR-210 in patients with SLE. The results of the study will contribute to a better understanding of miR network regulation in SLE in order to ultimately identify molecules that can be used in clinical practice as diagnostic or prognostic markers, treatment response markers, or even as potential future therapeutic targets. © Kourti M, Sokratous M, Katsiari CG.en
dc.language.isoenen
dc.sourceMediterranean Journal of Rheumatologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85106548220&doi=10.31138%2fMJR.31.1.71&partnerID=40&md5=36fcce3ebea7dec0ea128fbff09f85ad
dc.subjecthypoxia inducible factor 1alphaen
dc.subjectmicroRNA 21en
dc.subjectmicroRNA 210en
dc.subjectmitogen activated protein kinase 1en
dc.subjectmitogen activated protein kinase 3en
dc.subjectArticleen
dc.subjectcell hypoxiaen
dc.subjectcell isolationen
dc.subjectclinical articleen
dc.subjectcontrolled studyen
dc.subjectdisease classificationen
dc.subjectenzyme activityen
dc.subjectgene controlen
dc.subjectgene expressionen
dc.subjectgene functionen
dc.subjecthumanen
dc.subjecthuman cellen
dc.subjectpathogenesisen
dc.subjectPi3K/Akt signalingen
dc.subjectreal time polymerase chain reactionen
dc.subjectregulatory T lymphocyteen
dc.subjectsystemic lupus erythematosusen
dc.subjectTh17 cellen
dc.subjecttreatment responseen
dc.subjectGreek Rheumatology Society and Professional Association of Rheumatologistsen
dc.titleRegulation of microRNA in systemic lupus erythematosus: The role of miR-21 and miR-210en
dc.typejournalArticleen


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