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Craniopharyngiomas, including Recurrent Cases, Lack TERT Promoter Hotspot Mutations.
Fujio, Shingo; Juratli, Tareq A; Takajo, Tomoko; Arita, Kazunori; Nagano, Yushi; Yoshimoto, Koji; Nayyar, Naema; Curry, William T; Martinez-Lage, Maria; Cahill, Daniel P; Barker, Fred G; Brastianos, Priscilla K.
Afiliação
  • Fujio S; Divisions of Neuro-Oncology and Hematology/Oncology, Departments of Medicine and Neurology, Massachusetts General Hospital Cancer Center, Harvard Medical School.
  • Juratli TA; Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School.
  • Takajo T; Department of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University.
  • Arita K; Pituitary Disorders Center, Kagoshima University Hospital.
  • Nagano Y; Divisions of Neuro-Oncology and Hematology/Oncology, Departments of Medicine and Neurology, Massachusetts General Hospital Cancer Center, Harvard Medical School.
  • Yoshimoto K; Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School.
  • Nayyar N; Department of Neurosurgery, Faculty of Medicine and Carl Gustav, Carus University Hospital, Technische Universität Dresden.
  • Curry WT; Department of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University.
  • Martinez-Lage M; Department of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University.
  • Cahill DP; Department of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University.
  • Barker FG; Department of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University.
  • Brastianos PK; Pituitary Disorders Center, Kagoshima University Hospital.
Neurol Med Chir (Tokyo) ; 61(6): 385-391, 2021 Jun 15.
Article em En | MEDLINE | ID: mdl-33967180
Adamantinomatous craniopharyngiomas (ACP) are characterized by alterations in the CTNNB1 gene while almost all papillary craniopharyngiomas (PCP) harbor a canonical V600E mutation in the BRAF gene. Although other recurrent driver genes have not been described to date in craniopharyngiomas, the heterogeneous clinical course of these tumors might be associated with the acquisition of further genomic alterations. It is well known that telomerase reverse transcriptase (TERT) promoter (TERTp) alterations, including mutations or methylation, upregulate the expression of TERT and increase telomerase activity, promoting tumorigenesis. We investigated whether TERTp mutations or methylation are associated with tumor relapse in a subset of craniopharyngiomas. Samples from 42 patients with histologically confirmed craniopharyngioma were retrieved. We determined TERTp, BRAF, and CTNNB1 hotspot mutations in all samples using targeted sequencing and the TERTp methylation status by methylation-specific polymerase chain reaction (PCR) in 30 samples. While BRAF V600E mutations and CTNNB1 mutations were detected in 12 (28.6%) and 21 patients (50%) in the initial tumors and subsequent recurrences, respectively, none of the patients in our cohort, including those with multiple relapses, harbored a TERTp mutation. Furthermore, TERTp methylation was detected in 14 out of 24 cases (58.3%) with available primary samples; however, no correlation between TERTp methylation with the pathological subtype, genotype, or tumor aggressiveness was detected. These data suggest that elevated telomerase activity via acquisition of TERTp mutations is an infrequent pathway in the tumorigenesis of craniopharyngiomas, regardless of their clinical course.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Telomerase / Craniofaringioma Limite: Humans Idioma: En Revista: Neurol Med Chir (Tokyo) Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Telomerase / Craniofaringioma Limite: Humans Idioma: En Revista: Neurol Med Chir (Tokyo) Ano de publicação: 2021 Tipo de documento: Article