Comparative analyses identify molecular signature of MRI-classified SVZ-associated glioblastoma. Issue 8 (18th April 2017)

• Record Type: Journal Article
• Authors: Lin, Chin-Hsing Annie; Rhodes, Christopher T.; Lin, ChenWei; Phillips, Joanna J.; Berger, Mitchel S.
• Is Part Of: Cell cycle. Volume 16:Issue 8(2017)
• Page Start: 765
• Page End: 775
• Publication Date: 2017-04-18
• Subjects: Enhancer of zeste (Human- Gene: EZH2 -- Glioblastoma (GBM) -- Glioma stem cells (GSC) -- Histone lysine demethylase (KDM) -- Neural Stem Progenitor Cells (NSPCs) -- Protein: EZH2) -- subventricular zone (SVZ) -- tri-methylation at histone 3 lysine 27 (H3K27me3); Cell cycle -- Periodicals; 571.84377
• DOI: 10.1080/15384101.2017.1295186
• Languages: English
• ISSNs: 1538-4101

Abstract

ABSTRACT: Glioblastoma (GBM) is a highly aggressive brain cancer with limited therapeutic options. While efforts to identify genes responsible for GBM have revealed mutations and aberrant gene expression associated with distinct types of GBM, patients with GBM are often diagnosed and classified based on MRI features. Therefore, we seek to identify molecular representatives in parallel with MRI classification for group I and group II primary GBM associated with the subventricular zone (SVZ). As group I and II GBM contain stem-like signature, we compared gene expression profiles between these 2 groups of primary GBM and endogenous neural stem progenitor cells to reveal dysregulation of cell cycle, chromatin status, cellular morphogenesis, and signaling pathways in these 2 types of MRI-classified GBM. In the absence of IDH mutation, several genes associated with metabolism are differentially expressed in these subtypes of primary GBM, implicating metabolic reprogramming occurs in tumor microenvironment. Furthermore, histone lysine methyltransferase EZH2 was upregulated while histone lysine demethylases KDM2 and KDM4 were downregulated in both group I and II primary GBM. Lastly, we identified 9 common genes across large data sets of gene expression profiles among MRI-classified group I/II GBM, a large cohort of GBM subtypes from TCGA, and glioma stem cells by unsupervised clustering comparison. These commonly upregulated genes have known functions in cell cycle, centromere assembly, chromosome segregation, and mitotic progression. Our findings highlight altered expression of genes important in chromosome integrity across all GBM, suggesting a common mechanism of disrupted fidelity of chromosome structure in GBM.