<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/GSE315nnn/GSE315793/</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=GSE315793</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Schisandrin B exhibits anti-proliferative effects by inducing ferroptosis in pancreatic cancer</name><description>Pancreatic cancer (PC) is a lethal malignancy of the digestive system with an extremely low survival rate. Schisandrin B (Sch B) has demonstrated novel pre-clinical antitumor activity in several animal tumor models. However, it remains unclear whether Sch B exerts antitumor effects in PC. The molecular mechanisms underlying the antitumor properties of Sch B were explored using RNA sequencing.</description><dates><publication>2026/05/21</publication></dates><accession>GSE315793</accession><cross_references><GSM>GSM9437487</GSM><GSM>GSM9437488</GSM><GSM>GSM9437489</GSM><GSM>GSM9437490</GSM><GSM>GSM9437491</GSM><GSM>GSM9437492</GSM><GPL>24676</GPL><GSE>315793</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>