<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE336nnn/GSE336709/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Methylation profiling</omics_type><species>Homo sapiens</species><gds_type>Methylation profiling by genome tiling array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE336709</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>CpG Hypermethylation and WNT/AP-1 cooperativity Define the Epigenetic Landscape and a Clinical Subgroup of High-Risk Pediatric Adrenocortical Carcinoma [Methylation array]</name><description>Treatment of three adult ACC cell lines (H295R and ACC1, ACC2) with entinostat and decitbaine led to consistent dose-dependent changes in DNA methylation patterns. These findings support entinostat's potential to reverse high-risk epigenetic programs in pACT and highlight HDAC inhibition as a promising therapeutic avenue, particularly when combined with established treatments.</description><dates><publication>2026/08/12</publication></dates><accession>GSE336709</accession><cross_references><GSM>GSM9840949</GSM><GSM>GSM9840947</GSM><GSM>GSM9840958</GSM><GSM>GSM9840948</GSM><GSM>GSM9840956</GSM><GSM>GSM9840957</GSM><GSM>GSM9840946</GSM><GSM>GSM9840954</GSM><GSM>GSM9840955</GSM><GSM>GSM9840952</GSM><GSM>GSM9840953</GSM><GSM>GSM9840950</GSM><GSM>GSM9840951</GSM><GPL>33022</GPL><GSE>336709</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>