<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/GSE347nnn/GSE347712/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE347712</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of CT26 tumor-bearing mice treated with novel HDAC inhibitor GNTbm-38</name><description>Histone deacetylase inhibitors (HDACis) represent a promising therapeutic strategy in cancer treatment. In this study, we evaluated the therapeutic efficacy and molecular mechanisms of GNTbm-38, a novel HDAC inhibitor, using a syngeneic CT26 colon carcinoma tumor-bearing mouse model. BALB/c mice bearing subcutaneous CT26 tumors were treated with vehicle control or GNTbm-38. Bulk RNA-sequencing was performed on tumor tissues to characterize transcriptomic alterations induced by GNTbm-38. This dataset provides comprehensive gene expression profiles to elucidate the antitumor and immunomodulatory pathways regulated by GNTbm-38 in colorectal cancer.</description><dates><publication>2026/09/17</publication></dates><accession>GSE347712</accession><cross_references><GSM>GSM10059207</GSM><GSM>GSM10059206</GSM><GSM>GSM10059209</GSM><GSM>GSM10059208</GSM><GSM>GSM10059203</GSM><GSM>GSM10059202</GSM><GSM>GSM10059205</GSM><GSM>GSM10059204</GSM><GSM>GSM10059199</GSM><GSM>GSM10059210</GSM><GSM>GSM10059201</GSM><GSM>GSM10059211</GSM><GSM>GSM10059200</GSM><GPL>24247</GPL><GSE>347712</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>