<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/GSE293nnn/GSE293566/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE293566</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>SENP3 Drives HCC Redox Adaptation via THRAP3/NRF1 Axis [RNA-Seq]</name><description>SENP3 drives oxidative stress adaptation and ferroptosis resistance in HCC via THRAP3-mediated activation of NRF1. Targeting SENP3 with LNPs not only inhibits tumor progression but also enhances the efficacy of lenvatinib. These findings suggest SENP3 as a promising therapeutic target and biomarker for redox-based and ferroptosis-combined therapies in HCC.</description><dates><publication>2026/09/30</publication></dates><accession>GSE293566</accession><cross_references><GSM>GSM8885619</GSM><GSM>GSM8885620</GSM><GSM>GSM8885618</GSM><GSM>GSM8885617</GSM><GSM>GSM8885616</GSM><GSM>GSM8885615</GSM><GPL>24676</GPL><GSE>293566</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>