Next-generation whole exome sequencing of glioblastoma with a primitive neuronal component.

TitleNext-generation whole exome sequencing of glioblastoma with a primitive neuronal component.
Publication TypeJournal Article
Year of Publication2019
AuthorsXu G, Zheng H, Li JYi
JournalBrain Tumor Pathol
Volume36
Issue3
Pagination129-134
Date Published2019 Jul
ISSN1861-387X
KeywordsAdult, Aged, Aged, 80 and over, Brain Neoplasms, Class I Phosphatidylinositol 3-Kinases, Class Ia Phosphatidylinositol 3-Kinase, Female, Glioblastoma, Glioma, High-Throughput Nucleotide Sequencing, Humans, Male, Middle Aged, Mutation, Neuroectodermal Tumors, Primitive, Neurons, Phosphatidylinositol 3-Kinases, PTEN Phosphohydrolase, Tumor Suppressor Protein p53, Whole Exome Sequencing
Abstract

Glioblastoma with a primitive neuronal component (GBM-PN) was renamed from glioblastoma with primitive neuroectodermal tumor-like component (GBM-PNET) in the new WHO classification of tumors of the central nervous system in 2016. GBM-PN is a rare variant of glioblastoma. There were not so many publications on the investigation of GBM-PN. We did whole exome sequencing for 11 GBM-PN cases and found that the percentage of TP53, PIK3CA, PIK3R1, or PTEN mutation in our GBM-PN cases (72.7%, 27.3%, 27.3%, and 27.3% respectively) was much higher than that in cases in TCGA GBM 2008, TCGA GBM 2013, and TCGA lower-grade glioma databases. The findings indicate that GBM-PN is a distinct variant of glioblastoma. The next-generation sequencing can play a role in the diagnosis of GBM-PN especially for small biopsy cases. Eight out of 11 cases showed mutations in PTEN-PI3K pathway, which indicates that targeted therapeutic agents (PI3K inhibitors, mTORC1 inhibitors or dual PI3K/mTOR inhibitors) may be used for the treatment of GBM-PN in the future.

DOI10.1007/s10014-019-00334-1
Alternate JournalBrain Tumor Pathol
PubMed ID30715630
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