Function of Brg1 Chromatin Remodeling Factor in Sonic Hedgehog-Dependent Medulloblastoma Initiation and Maintenance
Abstract
Medulloblastoma is the most common malignant pediatric brain tumor. Overactive Shh signaling in cerebellum granule neuron precursors (CGNPs) is the leading cause of the childhood medulloblastoma (Shh-subtype). Current study focuses on the requirement of Brg1 in mouse model of Shh-type medulloblastoma. In vitro evidences showed that Brg1 is required for mitogenic target gene expression and proliferation in primary SmoM2 CGNP and tumor cultures. In vivo deletion of Brg1 through Math1-Cre dramatically decreased death rate and prolonged the survival resulted from Shh-type medulloblastoma. Induction of Brg1 deletion in subcutaneous transplantation led to tumor aggression significant blocked, the tumor proliferation decreased as well. RT-qPCR and WB confirmed that Shh-dependent mitogenic target genes are decreased by knockout of Brg1. RNA-seq analysis in the primary tumor showed the Brg1 deletion efficiently reversed the SmoM2 oncogenic effects in medulloblastoma development. This study provides evidences that chromatin remodeling complex BAF through Brg1 is a therapeutic target for Shh-type medulloblastoma. Considering H3K27me3 changes by Brg1 deletion, ChIP-seq of Brg1 and together with histone modifications will further uncover the molecular mechanisms underlining Shh-type medulloblastoma.
Document Details
- Document Type
- Technical Report
- Publication Date
- Oct 01, 2014
- Accession Number
- ADA614187
Entities
People
- Jiang Wu
- Xuanming Shi
Organizations
- University of Texas at Dallas