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Identification of miR-17, miR-21, miR-27a, miR-106b and miR-222 as endoplasmic reticulum stress-related potential biomarkers in circulation of patients with atherosclerosis

dc.contributor.authorTelkoparan-Akillilar, Pelin
dc.contributor.authorCevik, Dilek
dc.date.accessioned2026-10-09T21:47:12Z
dc.date.issued2021
dc.departmentYüksek İhtisas Üniversitesi
dc.description.abstractAtherosclerosis and related cardiovascular diseases are among the most common causes of death worldwide. Unfolded protein response, also known as Endoplasmic reticulum stress, has a critical role in many diseases including atherosclerosis. Small non-coding microRNAs (miRNA), which generally suppress gene expression, regulate UPR signalling and they may also be involved in the progression of atherosclerosis. We aim to investigate the expression levels of miR-17, miR-21, miR-27a, miR-106b, miR-222 and CHOP gene in circulation of atherosclerosis patients compared to healthy controls to establish a link between ER stress and atherosclerosis. miRNA containing whole RNA was isolated from blood samples of 25 patients with atherosclerosis and 26 healthy controls. Expression levels of miRNAs and CHOP were measured via Real Time PCR method. miR-17 and miR-106b were significantly increased while miR-21, miR-27a, and miR-222 were significantly decreased in patients compared to controls. CHOP gene was also dramatically and significantly induced in patient samples. miR-17, miR-21, miR-27a, miR-106b, miR-222 and CHOP were significantly differentially expressed in patients with atherosclerosis. Each miRNA and CHOP might regulate atherosclerotic plaque progression and they can be used as a biomarker in the diagnosis and follow-up of atherosclerosis-related cardiovascular diseases.
dc.description.sponsorshipScientific Research Projects Coordination Unit of Yuksek Ihtisas University [2018/01.001]
dc.description.sponsorshipThis work was supported by the Scientific Research Projects Coordination Unit of Yuksek Ihtisas University under Grant Number 2018/01.001.
dc.identifier.doi10.1007/s11033-021-06352-7
dc.identifier.endpage3513
dc.identifier.issn0301-4851
dc.identifier.issn1573-4978
dc.identifier.issue4
dc.identifier.orcid0000-0001-8940-3153
dc.identifier.orcid0000-0003-0337-0763
dc.identifier.pmid33860430
dc.identifier.scopus2-s2.0-85104746631
dc.identifier.scopusqualityQ2
dc.identifier.startpage3503
dc.identifier.urihttps://doi.org/10.1007/s11033-021-06352-7
dc.identifier.urihttps://hdl.handle.net/20.500.12794/3460
dc.identifier.volume48
dc.identifier.wosWOS:000640458800004
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.indekslendigikaynak.digerScience Citation Index Expanded (SCI-EXPANDED)
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofMolecular Biology Reports
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.relation.sdgGoal-03: Good Health and Well-Being
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260922
dc.subjectEr-Stress
dc.subjectAtherosclerosis
dc.subjectChop
dc.subjectMicrorna
dc.subjectMir-17
dc.subjectMir-21
dc.titleIdentification of miR-17, miR-21, miR-27a, miR-106b and miR-222 as endoplasmic reticulum stress-related potential biomarkers in circulation of patients with atherosclerosis
dc.typeArticle

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