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Ak Aksoy, Secil; Mutlu, Melis; Tunca, Berrin; Kocaeli, Hasan; Taskapilioglu, Mevlut Ozgur; Bekar, Ahmet; Tekin, Cagla; Argadal, Omer Gokay; Civan, Muhammet Nafi; Kaya, Ismail Seckin; Ocak, Pinar Eser; Tolunay, Sahsine
{ "@context": "https://schema.org/", "@id": 236606, "@type": "ScholarlyArticle", "creator": [ { "@type": "Person", "affiliation": "Bursa Uludag Univ, Inegol Vocat Sch, Bursa, Turkey", "name": "Ak Aksoy, Secil" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Med Biol, Bursa, Turkey", "name": "Mutlu, Melis" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Med Biol, Bursa, Turkey", "name": "Tunca, Berrin" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", "name": "Kocaeli, Hasan" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", "name": "Taskapilioglu, Mevlut Ozgur" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", "name": "Bekar, Ahmet" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Med Biol, Bursa, Turkey", "name": "Tekin, Cagla" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", "name": "Argadal, Omer Gokay" }, { "@type": "Person", "affiliation": "Uludag Univ, Fac Med, Bursa, Turkey", "name": "Civan, Muhammet Nafi" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", "name": "Kaya, Ismail Seckin" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", "name": "Ocak, Pinar Eser" }, { "@type": "Person", "affiliation": "Bursa Uludag Univ, Fac Med, Dept Pathol, Bursa, Turkey", "name": "Tolunay, Sahsine" } ], "datePublished": "2021-01-01", "description": "Objective: This study was designed to conduct molecular classification based on IDH1/2, TERT, ATRX, and DAXX changes in pediatric and adult primary glioblastoma (GB) and to analyze the potential interaction of LncRNA MALAT1 in the determined homogeneous subgroups. Methods: We analyzed the expression profiles of ATRX/DAXX and MALAT1 using the qRT-PCR method and IDH and TERT mutation status using DNA sequencing analysis in 85 primary pediatric and adult GB patients. Results: IDH1 mutation was observed in 5 (5.88%) and TERT mutation in 65 (76.47%) primary pediatric and adult GB patients. ATRX and DAXX were detected in 18 (21.18%) and 7 (8.24%) patients. TERT mutation and loss of ATRX/DAXX were associated with short overall survival (p < 0.001, p < 0.001, respectively). Patients carrying especially TERT C228T mutation had worse prognosis (p < 0.001). Six subgroups were obtained from the genetic analysis. Among the subgroups, MALAT1 was highly expressed in group A that had a single TERT mutation as compared to that in groups D and E (p = 0.001 and p < 0.001, respectively); further, high MALAT1 expression was associated with worse prognosis in patients with C228T mutation (p < 0.001). Conclusions: Our findings highlight that the presence of TERT C228T mutation and expression of MALAT1 can be used as primary targets during the follow-up of primary GB patients and in the development of new treatment strategies.", "headline": "Coexistence of TERT C228T mutation and MALAT1 dysregulation in primary glioblastoma: new prognostic and therapeutic targets", "identifier": 236606, "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", "license": "http://www.opendefinition.org/licenses/cc-by", "name": "Coexistence of TERT C228T mutation and MALAT1 dysregulation in primary glioblastoma: new prognostic and therapeutic targets", "url": "https://aperta.ulakbim.gov.tr/record/236606" }
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