Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/24548
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dc.contributor.authorGüler, Gülnur-
dc.date.accessioned2022-02-21T10:17:52Z-
dc.date.available2022-02-21T10:17:52Z-
dc.date.issued2009-07-
dc.identifier.citationÇeçener, G. vd. (2009). "Investigation of MMAC/PTEN gene mutations and protein expression in low grade gliomas". Cellular and Molecular Neurobiology, 29(5), 733-738.en_US
dc.identifier.issn0272-4340-
dc.identifier.urihttps://doi.org/10.1007/s10571-009-9397-z-
dc.identifier.urihttps://link.springer.com/article/10.1007/s10571-009-9397-z-
dc.identifier.urihttp://hdl.handle.net/11452/24548-
dc.description.abstractThe MMAC/PTEN tumor suppressor gene has an essential biological role in the formation of glioblastomas. It is known that there are variations in genetic alterations in tumors that develop in patients with different ethnic backgrounds; thus, we aimed to evaluate the incidence of MMAC/PTEN mutations and protein expression among various low grade gliomas of Turkish patients. We investigated 28 low grade gliomas for mutations of the MMAC/PTEN gene using single strand conformational polymorphism method followed by DNA sequencing. Additionally, the level of MMAC/PTEN protein expression in the tissues of 26 tumors was assessed by immunohistochemistry. In our investigation, MMAC/PTEN mutations were detected in 2 of 28 tumors (7.14%). One novel sequence variant G -> A transition at codon 159 was identified. This missense variation was a result of an alteration from AGG (Arginine) to AAG (Lysine). Moreover, it was observed that MMAC/PTEN protein expression was reduced to 73.08% of tumors. In conclusion, reduced MMAC/PTEN expression by genetic and/or epigenetic mechanisms in low grade gliomas might be associated with glioma tumorigenesis.en_US
dc.language.isoenen_US
dc.publisherSpringer/Plenum Publishersen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectIHCen_US
dc.subjectLow grade gliomasen_US
dc.subjectMMAC/PTENen_US
dc.subjectSequencingen_US
dc.subjectSSCPen_US
dc.subjectTurkish populationen_US
dc.subjectGlioblastoma-multiformeen_US
dc.subjectSequence-analysisen_US
dc.subjectPten mutationsen_US
dc.subjectPten/mmac1en_US
dc.subjectCanceren_US
dc.subjectP53en_US
dc.subjectCell Biologyen_US
dc.subjectNeurosciences & neurologyen_US
dc.subject.meshAdolescenten_US
dc.subject.meshAdulten_US
dc.subject.meshAmino acid substitutionen_US
dc.subject.meshBase sequenceen_US
dc.subject.meshDNA mutational analysisen_US
dc.subject.meshFemaleen_US
dc.subject.meshGliomaen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshMolecular sequence dataen_US
dc.subject.meshMutationen_US
dc.subject.meshPTEN phosphohydrolaseen_US
dc.titleInvestigation of MMAC/PTEN gene mutations and protein expression in low grade gliomasen_US
dc.typeArticleen_US
dc.identifier.wos000266983100013tr_TR
dc.identifier.scopus2-s2.0-67650806143tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Nöroşirürji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen- Edebiyat Fakültesi/Biyoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-7687-3284tr_TR
dc.contributor.orcid0000-0001-7904-883Xtr_TR
dc.contributor.orcid0000-0002-1619-6680tr_TR
dc.contributor.orcid0000-0002-3820-424Xtr_TR
dc.identifier.startpage733tr_TR
dc.identifier.endpage738tr_TR
dc.identifier.volume29tr_TR
dc.identifier.issue5tr_TR
dc.relation.journalCellular and Molecular Neurobiologyen_US
dc.contributor.buuauthorÇeçener, Gülşah-
dc.contributor.buuauthorTunca, Berrin-
dc.contributor.buuauthorEgeli, Ünal-
dc.contributor.buuauthorBekar, Ahmet-
dc.contributor.buuauthorVatan, Özgür-
dc.contributor.buuauthorTolunay, Şahsine-
dc.contributor.researcheridAAI-1612-2021tr_TR
dc.contributor.researcheridO-7508-2015tr_TR
dc.contributor.researcheridAAH-1420-2021tr_TR
dc.contributor.researcheridABI-6078-2020tr_TR
dc.contributor.researcheridAAP-9988-2020tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed19350382tr_TR
dc.subject.wosCell biologyen_US
dc.subject.wosNeurosciencesen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid6508156530tr_TR
dc.contributor.scopusid6602965754tr_TR
dc.contributor.scopusid55665145000tr_TR
dc.contributor.scopusid6603677218tr_TR
dc.contributor.scopusid16235098100tr_TR
dc.contributor.scopusid6602604390tr_TR
dc.subject.scopusTensins; Phosphatases; Phosphatidylinositol 3,4,5-Triphosphateen_US
dc.subject.emtreeArginineen_US
dc.subject.emtreeDNAen_US
dc.subject.emtreeLysineen_US
dc.subject.emtreePhosphatidylinositol 3,4,5 trisphosphate 3 phosphataseen_US
dc.subject.emtreeAdolescenten_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCarcinogenesisen_US
dc.subject.emtreeClinical articleen_US
dc.subject.emtreeCodonen_US
dc.subject.emtreeDNA sequenceen_US
dc.subject.emtreeEpigeneticsen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeGene mutationen_US
dc.subject.emtreeGenetic variabilityen_US
dc.subject.emtreeGliomaen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeImmunohistochemistryen_US
dc.subject.emtreeIncidenceen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMissense mutationen_US
dc.subject.emtreeMMAC geneen_US
dc.subject.emtreeNucleotide sequenceen_US
dc.subject.emtreePriority journaltr_TR
dc.subject.emtreeProtein expressionen_US
dc.subject.emtreePTEN geneen_US
dc.subject.emtreeSingle strand conformation polymorphismen_US
dc.subject.emtreeTumor suppressor geneen_US
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