<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(12)</volume><submitter>Jha P</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Pediatric glioblastoma multiforme (GBM) is rare, and there is a single study, a seminal discovery showing association of histone H3.3 and isocitrate dehydrogenase (IDH)1 mutation with a DNA methylation signature. The present study aims to validate these findings in an independent cohort of pediatric GBM, compare it with adult GBM, and evaluate the involvement of important functionally altered pathways.&lt;h4>Methods&lt;/h4>Genome-wide methylation profiling of 21 pediatric GBM cases was done and compared with adult GBM data (GSE22867). We performed gene mutation analysis of IDH1 and H3 histone family 3A (H3F3A), status evaluation of glioma cytosine-phosphate-guanine island methylator phenotype (G-CIMP), and Gene Ontology analysis. Experimental evaluation of reactive oxygen spec</pubmed_abstract><journal>Neuro-oncology</journal><pagination>1607-17</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4232083</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genome-wide methylation profiling identifies an essential role of reactive oxygen species in pediatric glioblastoma multiforme and validates a methylome specific for H3 histone family 3A with absence of G-CIMP/isocitrate dehydrogenase 1 mutation.</pubmed_title><pmcid>PMC4232083</pmcid><pubmed_authors>Pia Patric IR</pubmed_authors><pubmed_authors>Somasundaram K</pubmed_authors><pubmed_authors>Sarkar C</pubmed_authors><pubmed_authors>Suri V</pubmed_authors><pubmed_authors>Sharma MC</pubmed_authors><pubmed_authors>Arivazhagan A</pubmed_authors><pubmed_authors>Pathak P</pubmed_authors><pubmed_authors>Jha P</pubmed_authors><pubmed_authors>Pal J</pubmed_authors><pubmed_authors>Thinagararanjan S</pubmed_authors><pubmed_authors>Suri A</pubmed_authors><pubmed_authors>Gupta D</pubmed_authors><pubmed_authors>Shukla S</pubmed_authors><pubmed_authors>Santosh V</pubmed_authors><pubmed_authors>Sharma V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-wide methylation profiling identifies an essential role of reactive oxygen species in pediatric glioblastoma multiforme and validates a methylome specific for H3 histone family 3A with absence of G-CIMP/isocitrate dehydrogenase 1 mutation.</name><description>&lt;h4>Background&lt;/h4>Pediatric glioblastoma multiforme (GBM) is rare, and there is a single study, a seminal discovery showing association of histone H3.3 and isocitrate dehydrogenase (IDH)1 mutation with a DNA methylation signature. The present study aims to validate these findings in an independent cohort of pediatric GBM, compare it with adult GBM, and evaluate the involvement of important functionally altered pathways.&lt;h4>Methods&lt;/h4>Genome-wide methylation profiling of 21 pediatric GBM cases was done and compared with adult GBM data (GSE22867). We performed gene mutation analysis of IDH1 and H3 histone family 3A (H3F3A), status evaluation of glioma cytosine-phosphate-guanine island methylator phenotype (G-CIMP), and Gene Ontology analysis. Experimental evaluation of reactive oxygen spec</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Dec</publication><modification>2026-05-01T23:00:38.255Z</modification><creation>2025-05-29T19:25:40.685Z</creation></dates><accession>S-EPMC4232083</accession><cross_references><pubmed>24997139</pubmed><doi>10.1093/neuonc/nou113</doi></cross_references></HashMap>