Publication:
NEAT1 Is a novel oncogenic LncRNA and correlated with miR-143 in pediatric oligodendrogliomas

dc.contributor.authorAk Aksoy, Seçil
dc.contributor.authorMutlu, Melis
dc.contributor.authorBalçin, Rabia Nur
dc.contributor.authorTaşkapılıoğlu, Mevlut Özgür
dc.contributor.authorTekin, Çağla
dc.contributor.authorKaya, Seçkin
dc.contributor.authorCivan, Muhammet Nafi
dc.contributor.authorKocaeli, Hasan
dc.contributor.authorBekar, Ahmet
dc.contributor.authorEser Ocak, Pınar
dc.contributor.authorÇeçener, Gülşah
dc.contributor.authorEgeli, Ünal
dc.contributor.authorTolunay, Şahsine
dc.contributor.authorTunca, Berrin
dc.contributor.buuauthorAk Aksoy, Seçil
dc.contributor.buuauthorMutlu, Melis
dc.contributor.buuauthorBALÇIN, RABİA NUR
dc.contributor.buuauthorTAŞKAPILIOĞLU, MEVLÜT ÖZGÜR
dc.contributor.buuauthorTekin, Çağla
dc.contributor.buuauthorKAYA, İSMAİL SEÇKİN
dc.contributor.buuauthorCivan, Muhammet Nafi
dc.contributor.buuauthorKOCAELİ, HASAN
dc.contributor.buuauthorBEKAR, AHMET
dc.contributor.buuauthorEser Ocak, Pınar
dc.contributor.buuauthorÇEÇENER, GÜLŞAH
dc.contributor.buuauthorEGELİ, ÜNAL
dc.contributor.buuauthorTOLUNAY, ŞAHSİNE
dc.contributor.buuauthorTUNCA, BERRİN
dc.contributor.departmentBursa Uludağ Üniversitesi/İnegöl Meslek Yüksekokulu.
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Beyin Cerrahisi Anabilim Dalı.
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.
dc.contributor.orcid0000-0001-5472-9065
dc.contributor.orcid0000-0002-4256-2250
dc.contributor.orcid0000-0003-0132-9927
dc.contributor.orcid0000-0002-3820-424X
dc.contributor.orcid0000-0001-7904-883X
dc.contributor.orcid0000-0002-1619-6680
dc.contributor.researcheridADM-8457-2022
dc.contributor.researcheridFPB-0403-2022
dc.contributor.researcheridGXV-3107-2022
dc.contributor.researcheridAAW-5254-2020
dc.contributor.researcheridGDC-6329-2022
dc.contributor.researcheridJGS-1849-2023
dc.contributor.researcheridHKP-0793-2023
dc.contributor.researcheridFDK-3229-2022
dc.contributor.researcheridCGB-7869-2022
dc.contributor.researcheridAAI-2073-2021
dc.contributor.researcheridAAP-9988-2020
dc.contributor.researcheridAAH-1420-2021
dc.contributor.researcheridAAI-1612-2021
dc.contributor.researcheridABI-6078-2020
dc.date.accessioned2024-11-07T11:22:23Z
dc.date.available2024-11-07T11:22:23Z
dc.date.issued2021-03-19
dc.description.abstractIntroduction: The noncoding RNAs (ncRNAs) play a role in biological processes of various cancers including gliomas. The majority of these transcripts are uniquely expressed in differentiated tissues or specific glioma types. Pediatric oligodendroglioma (POG) is a rare subtype of diffuse glioma and accounts for <1% of pediatric brain tumors. Because histologically POG resembles adult OG, the same treatment is applied as adults. However, the significance in predicting outcomes in POG patients is unclear. In this study, we aimed to investigate the prognostic significance of expression -profiles of microRNA (miRNA) and long noncoding RNA -(LncRNA) in POGs. Methods: We investigated the levels of 13 known miRNAs and 6 LncRNAs in tumor samples from 9 patients with primary POG by using RT-PCR and analyzed their association with outcomes. Results: The expression levels of miR-21, miR-106a, miR-10b, and LncRNA NEAT1 were higher, and the expression level of miR-143 was lower in POG tissues compared with normal brain tissues (p = 0.006, p = 0.032, p = 0.034, p = 0.002, and p = 0.001, respectively). High levels of NEAT1 and low expression of miR-143 were associated with decreased probability of short disease-free survival (p = 0.018 and p = 0.022, respectively). Discussion: NEAT1 and miR-143 levels could serve as reciprocal prognostic predictors of disease progression in patients with POG. New treatment models to regulate the expression levels of NEAT1 and miR-143 will bring a new approach to the therapy of POG.
dc.identifier.doi10.1159/000514330
dc.identifier.endpage139
dc.identifier.issn1016-2291
dc.identifier.issue2
dc.identifier.startpage133
dc.identifier.urihttps://doi.org/10.1159/000514330
dc.identifier.urihttps://karger.com/pne/article-abstract/56/2/133/277709/NEAT1-Is-a-Novel-Oncogenic-LncRNA-and-Correlated?redirectedFrom=fulltext
dc.identifier.urihttps://hdl.handle.net/11452/47572
dc.identifier.volume56
dc.identifier.wos000632545000001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherKarger
dc.relation.bapKUAP(T)-2019/2
dc.relation.journalPediatric Neurosurgery
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectPediatric oligodendroglioma
dc.subjectPrognosis
dc.subjectLncrna neat1
dc.subjectMir-143
dc.subjectNeurosciences & neurology
dc.subjectPediatrics
dc.subjectSurgery
dc.titleNEAT1 Is a novel oncogenic LncRNA and correlated with miR-143 in pediatric oligodendrogliomas
dc.typeArticle
dspace.entity.typePublication
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