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ABSTRACT: Background
Using a pathway-focused approach, we aimed to provide a subgroup-specific basis for finding novel therapeutic strategies and further refinement of the risk stratification in pediatric medulloblastoma.Method
Based on genome-wide Cox regression and Gene Set Enrichment Analysis, we investigated prognosis-related signaling pathways and core genes in pediatric medulloblastoma subgroups using 530 patient data from Medulloblastoma Advanced Genomic International Consortium (MAGIC) project. We further examined the relationship between expression of the prognostic core genes and frequent chromosome aberrations using broad range copy number change data.Results
In SHH subgroup, relatively high expression of the core genes involved in p53, PLK1, FOXM1, and Aurora B si
SUBMITTER: Park AK
PROVIDER: S-EPMC6560914 | biostudies-literature | 2019 Jun
REPOSITORIES: biostudies-literature