The genetic landscape of ganglioglioma

Melike Pekmezci(University of California, San Francisco), Javier Villanueva-Meyer(University of California, San Francisco), Benjamin Goode(University of California, San Francisco), Jessica Van Ziffle(University of California, San Francisco), Courtney Onodera(University of California, San Francisco), James P. Grenert(University of California, San Francisco), Boris C. Bastian(University of California, San Francisco), Gabriel Chamyan(Miami Children's Hospital), Ossama Maher(Miami Children's Hospital), Ziad Khatib(Miami Children's Hospital), Bette K. Kleinschmidt‐DeMasters(University of Colorado Anschutz Medical Campus), David Samuel(Children's Hospital Central California), Sabine Mueller(University of California, San Francisco), Anuradha Banerjee(University of California, San Francisco), Jennifer Clarke(University of California, San Francisco), Tabitha Cooney(UCSF Benioff Children's Hospital), Joseph C. Torkildson(UCSF Benioff Children's Hospital), Nalin Gupta(University of California, San Francisco), Philip V. Theodosopoulos(University of California, San Francisco), Edward F. Chang(University of California, San Francisco), Mitchel S. Berger(University of California, San Francisco), Andrew W. Bollen(University of California, San Francisco), Arie Perry(University of California, San Francisco), Tarık Tihan(University of California, San Francisco), David A. Solomon(University of California, San Francisco)
Acta Neuropathologica Communications
June 7, 2018
Cited by 202Open Access
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Abstract

Ganglioglioma is the most common epilepsy-associated neoplasm that accounts for approximately 2% of all primary brain tumors. While a subset of gangliogliomas are known to harbor the activating p.V600E mutation in the BRAF oncogene, the genetic alterations responsible for the remainder are largely unknown, as is the spectrum of any additional cooperating gene mutations or copy number alterations. We performed targeted next-generation sequencing that provides comprehensive assessment of mutations, gene fusions, and copy number alterations on a cohort of 40 gangliogliomas. Thirty-six harbored mutations predicted to activate the MAP kinase signaling pathway, including 18 with BRAF p.V600E mutation, 5 with variant BRAF mutation (including 4 cases with novel in-frame insertions at p.R506 in the β3-αC loop of the kinase domain), 4 with BRAF fusion, 2 with KRAS mutation, 1 with RAF1 fusion, 1 with biallelic NF1 mutation, and 5 with FGFR1/2 alterations. Three gangliogliomas with BRAF p.V600E mutation had concurrent CDKN2A homozygous deletion and one additionally harbored a subclonal mutation in PTEN. Otherwise, no additional pathogenic mutations, fusions, amplifications, or deletions were identified in any of the other tumors. Amongst the 4 gangliogliomas without canonical MAP kinase pathway alterations identified, one epilepsy-associated tumor in the temporal lobe of a young child was found to harbor a novel ABL2-GAB2 gene fusion. The underlying genetic alterations did not show significant association with patient age or disease progression/recurrence in this cohort. Together, this study highlights that ganglioglioma is characterized by genetic alterations that activate the MAP kinase pathway, with only a small subset of cases that harbor additional pathogenic alterations such as CDKN2A deletion.


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