Title | Next-generation whole exome sequencing of glioblastoma with a primitive neuronal component. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Xu G, Zheng H, Li JYi |
Journal | Brain Tumor Pathol |
Volume | 36 |
Issue | 3 |
Pagination | 129-134 |
Date Published | 2019 Jul |
ISSN | 1861-387X |
Keywords | Adult, 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. |
DOI | 10.1007/s10014-019-00334-1 |
Alternate Journal | Brain Tumor Pathol |
PubMed ID | 30715630 |
Related Faculty:
Hongwu Zheng, Ph.D.