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Analysis of EZH2: micro-RNA network in low and high grade astrocytic tumors.

Authors :
Sharma V
Purkait S
Takkar S
Malgulwar PB
Kumar A
Pathak P
Suri V
Sharma MC
Suri A
Kale SS
Kulshreshtha R
Sarkar C
Source :
Brain tumor pathology [Brain Tumor Pathol] 2016 Apr; Vol. 33 (2), pp. 117-28. Date of Electronic Publication: 2016 Jan 08.
Publication Year :
2016

Abstract

Enhancer of Zeste homologue2 (EZH2) is an epigenetic regulator that functions as oncogene in astrocytic tumors, however, EZH2 regulation remains little studied. In this study, we measured EZH2 levels in low (Gr-II,DA) and high grade (Gr-IV,GBM) astrocytic tumors and found significant increased EZH2 transcript level with grade(median DA-8.5, GBM-28.9).However, a different trend was reflected in protein levels, with GBMs showing high EZH2 LI(median-26.5) compared to DA (median 0.3). This difference in correlation of EZH2 protein and RNA levels suggested post-transcriptional regulation of EZH2, likely mediated by miRNAs. We selected eleven miRNAs that strongly predicted to target EZH2 and measured their expression. Three miRNAs (miR-26a-5p,miR27a-3p and miR-498) showed significant correlation with EZH2 protein, suggesting them as regulators of EZH2, however miR-26a-5p levels decreased with grade. ChIP analyses revealed H3K27me3 modifications in miR-26a promoter suggesting feedback loop between EZH2 and miR26a. We further measured six downstream miRNA targets of EZH2 and found significant downregulation of four (miR-181a/b and 200b/c) in GBM. Interestingly, EZH2 associated miRNAs were predicted to target 25 genes in glioma-pathway, suggesting their role in tumor formation or progression. Collectively, our work suggests EZH2 and its miRNA interactors may serve as promising biomarkers for progression of astrocytic tumors and may offer novel therapeutic strategies.

Details

Language :
English
ISSN :
1861-387X
Volume :
33
Issue :
2
Database :
MEDLINE
Journal :
Brain tumor pathology
Publication Type :
Academic Journal
Accession number :
26746204
Full Text :
https://doi.org/10.1007/s10014-015-0245-1