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dc.contributor.authorÖzbayer, Cansu
dc.contributor.authorDeğirmenci, İrfan
dc.contributor.authorÜstüner, Derya
dc.contributor.authorAk, Güntulu
dc.contributor.authorSaydam, Faruk
dc.contributor.authorÇolak, Ertuğrul
dc.contributor.authorGüneş, Hasan Veysi
dc.contributor.authorMetintaş, Muzaffer
dc.date.accessioned2020-12-19T19:55:57Z
dc.date.available2020-12-19T19:55:57Z
dc.date.issued2016
dc.identifier.citationOzbayer, C., Degirmenci, I., Ustuner, D., Ak, G., Saydam, F., Colak, E., Gunes, H.V. & Metintas, M. (2016). miRSNPs of miR1274 and miR3202 genes that target MeCP2 and DNMT3b are associated with lung cancer risk: A study conducted on MassARRAY genotyping. Journal of Environmental Pathology Toxicology and Oncology, 35(3), 222-235. https://doi.org/10.1615/JEnvironPatholToxicolOncol.2016016320en_US
dc.identifier.issn0731-8898
dc.identifier.issn2162-6537
dc.identifier.urihttps://doi.org/10.1615/JEnvironPatholToxicolOncol.2016016320
dc.identifier.urihttps://hdl.handle.net/11436/2640
dc.descriptionOzbayer, Cansu/0000-0002-1120-1874; Colak, Ertugrul/0000-0003-3251-1043en_US
dc.descriptionWOS: 000387794000003en_US
dc.description.abstractGenetic variants of miRNAs that target DNMTs and MBDs involved in DNA methylation were scanned with current databases, and 35 miRSNPs in 22 miRNA genes were identified. the aim of the study was to determine the association between these variants of miRNA genes and lung cancer (LC). DNA samples were isolated from blood samples and genotyped using a Sequenom MassARRAY System. An association between the rs188912830 gene variant of miR3202 that targets the MeCP2 protein and LC was indicated in both subtypes. the presence of the C-allele in patients with LC and its subtypes was significantly lower, and the absence of the C-allele was determined to increase the risk of LC by 7,429-times compared to the presence (p=0,010). the rs318039 gene variant of miR1274 that targets DNMT3b was found to be associated with LC subtypes. When allele distributions were compared, the numbers of individuals with the C-allele were significantly lower in the NSCLC and SCLC groups. No significant associations were found for the rs72563729 variant of the miR200b gene that targets DNMT3a or for the rs145416750 variant of the miR513c gene that targets TRDMT1. the other 33 variants were found to be ancestral genotypes. Consequently, rs188912830 and rs318039 variations were associated with LC subtypes. Importantly, this study is the first to indicate the functional characterisation of miRSNPs of genes that target DNA methylation.en_US
dc.description.sponsorshipResearch Foundation of Eskisehir Osmangazi University, TurkeyEskisehir Osmangazi University [201241020]en_US
dc.description.sponsorshipThis study was supported by grant 201241020 from the Research Foundation of Eskisehir Osmangazi University, Turkey.en_US
dc.language.isoengen_US
dc.publisherBegell House Incen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectLung canceren_US
dc.subjectDNA methylationen_US
dc.subjectDNA methyltransferasesen_US
dc.subjectMassARRAYen_US
dc.subjectMethyl-binding proteinsen_US
dc.subjectmiRSNPen_US
dc.titlemiRSNPs of miR1274 and miR3202 genes that target MeCP2 and DNMT3b are associated with lung cancer risk: A study conducted on MassARRAY genotypingen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorSaydam, Faruk
dc.identifier.doi10.1615/JEnvironPatholToxicolOncol.2016016320
dc.identifier.volume35en_US
dc.identifier.issue3en_US
dc.identifier.startpage222en_US
dc.identifier.endpage235en_US
dc.relation.journalJournal of Environmental Pathology Toxicology and Oncologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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