Craniopharyngiomas, including Recurrent Cases, Lack TERT Promoter Hotspot Mutations.

Neurol Med Chir (Tokyo)

Divisions of Neuro-Oncology and Hematology/Oncology, Departments of Medicine and Neurology, Massachusetts General Hospital Cancer Center, Harvard Medical School.

Published: June 2021

AI Article Synopsis

  • Adamantinomatous craniopharyngiomas (ACP) are linked to CTNNB1 gene changes, while papillary craniopharyngiomas (PCP) mostly have a BRAF V600E mutation.
  • Research indicates that TERT promoter (TERTp) alterations may impact tumor relapse, but this study found no TERTp mutations among 42 craniopharyngioma samples despite frequent BRAF and CTNNB1 mutations.
  • TERTp methylation was found in 58.3% of initial samples but did not correlate with tumor type, genotype, or aggressiveness, suggesting TERTp mutations play a limited role in craniopharyngioma development.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258007PMC
http://dx.doi.org/10.2176/nmc.rc.2020-0339DOI Listing

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