Publication:
Microrna analysis of human decidua mesenchymal stromal cells from preeclampsia patients

dc.contributor.coauthorKamali Simsek, Nilüfer
dc.contributor.coauthorBenian, Ali
dc.contributor.coauthorÇelik, Hale Göksever
dc.contributor.coauthorGünel, Tuba
dc.contributor.departmentN/A
dc.contributor.departmentN/A
dc.contributor.departmentN/A
dc.contributor.kuauthorŞevgin, Kübra
dc.contributor.kuauthorErgün, Yağmur
dc.contributor.kuauthorKarahüseyinoğlu, Serçin
dc.contributor.kuprofileN/A
dc.contributor.kuprofileMaster Student
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteN/A
dc.contributor.schoolcollegeinstituteGraduate School of Health Sciences
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.yokidN/A
dc.contributor.yokidN/A
dc.contributor.yokid110772
dc.date.accessioned2024-11-09T23:06:49Z
dc.date.issued2021
dc.description.abstractIntroduction: In preeclampsia (PE), human decidua mesenchymal stromal cells (hDMSCs) are exposed to abnormally high levels of oxidative stress and inflammatory factors circulating in the maternal blood. MicroRNAs (miRNAs) have been shown to have a significant impact on the differentiation, maturation and function of mesenchymal stromal cells (MSCs). Our aim in the present study is firstly to investigate differentially expressed miRNA levels to be used as a biomarker in the early detection of PE and secondly to investigate whether those differentially expressed miRNAs in hDMSCs have an effect on the pathogenesis of PE. Methods: This study covers miRNA expression analysis of hDMSCs from 7 PE patient and 7 healthy pregnant women and is a preliminary study to investigate putative biomarkers. After cell culture and cell sorting, total RNA including miRNAs were isolated from hDMSCs. Let 7b 3p, let 7f 1 3p, miR-191-3p, miR-550a-5p, miR-33b-3p and miR-425-3p were used for miRNA analysis and U6 snRNA was used for normalization of the samples. MiRNA analysis was performed by droplet digital polymerase chain reaction (ddPCR) method and obtained results were evaluated statistically. Results: As a result of the analysis, it was observed that the levels of hsa-miR-33b-3p significantly (AUC: 0.93, p = 0.04, fold change: 4.5) increased in hDMSC of PE patients compared to healthy controls. However, let-7b-3p, let7f-1-3p, miR-191-3p, miR-550a-5p, and miR-425-3p were not considered as significant because they did not meet the p < 0,05 requirement. Discussion: Within the scope of the study, it is predicted that miR-33b-3p (p = 0.004, AUC = 0.93) can be used as a biomarker in detecting PE.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsorshipScientific Research Projects Coordination Unit of Istanbul University [28953, TSA-2018-29454] This study was funded by Scientific Research Projects Coordination Unit of Istanbul University (Project number: 28953) and Scientific Research Projects Coordination Unit of Istanbul University-Cerrahpasa (Project number: TSA-2018-29454) .
dc.description.volume115
dc.identifier.doi10.1016/j.placenta.2021.09.004
dc.identifier.eissn1532-3102
dc.identifier.issn0143-4004
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85114787080
dc.identifier.urihttp://dx.doi.org/10.1016/j.placenta.2021.09.004
dc.identifier.urihttps://hdl.handle.net/20.500.14288/9042
dc.identifier.wos714647400002
dc.keywordsPreeclampsia
dc.keywordsHuman decidua mesenchymal stromal cell
dc.keywordsMicrorna
dc.keywordsDroplet digital pcr
dc.keywordsStem-cells
dc.keywordsChorionic villi
dc.keywordsExpression
dc.keywordsPlacenta
dc.keywordsMir-16
dc.keywordsFetal
dc.keywordsAngiogenesis
dc.keywordsPregnancies
dc.keywordsDifferentiation
dc.keywordsProliferation
dc.languageEnglish
dc.publisherW B Saunders Co Ltd
dc.sourcePlacenta
dc.subjectBiology
dc.subjectObstetrics
dc.subjectGynecology
dc.titleMicrorna analysis of human decidua mesenchymal stromal cells from preeclampsia patients
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authoridN/A
local.contributor.authorid0000-0001-5811-8616
local.contributor.authorid0000-0001-5531-2587
local.contributor.kuauthorSevgin, Kübra
local.contributor.kuauthorErgün, Yağmur
local.contributor.kuauthorKarahüseyinoğlu, Serçin

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