Dergi makalesi Açık Erişim

Coexistence of TERT C228T mutation and MALAT1 dysregulation in primary glioblastoma: new prognostic and therapeutic targets

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


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    "creators": [
      {
        "affiliation": "Bursa Uludag Univ, Inegol Vocat Sch, Bursa, Turkey", 
        "name": "Ak Aksoy, Secil"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Med Biol, Bursa, Turkey", 
        "name": "Mutlu, Melis"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Med Biol, Bursa, Turkey", 
        "name": "Tunca, Berrin"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", 
        "name": "Kocaeli, Hasan"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", 
        "name": "Taskapilioglu, Mevlut Ozgur"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", 
        "name": "Bekar, Ahmet"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Med Biol, Bursa, Turkey", 
        "name": "Tekin, Cagla"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", 
        "name": "Argadal, Omer Gokay"
      }, 
      {
        "affiliation": "Uludag Univ, Fac Med, Bursa, Turkey", 
        "name": "Civan, Muhammet Nafi"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", 
        "name": "Kaya, Ismail Seckin"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Neurosurg, Bursa, Turkey", 
        "name": "Ocak, Pinar Eser"
      }, 
      {
        "affiliation": "Bursa Uludag Univ, Fac Med, Dept Pathol, Bursa, Turkey", 
        "name": "Tolunay, Sahsine"
      }
    ], 
    "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.", 
    "doi": "10.1080/01616412.2021.1948738", 
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    "journal": {
      "issue": "11", 
      "pages": "916-925", 
      "title": "NEUROLOGICAL RESEARCH", 
      "volume": "43"
    }, 
    "license": {
      "id": "cc-by"
    }, 
    "publication_date": "2021-01-01", 
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    "title": "Coexistence of TERT C228T mutation and MALAT1 dysregulation in primary glioblastoma: new prognostic and therapeutic targets"
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