<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/GSE338nnn/GSE338233/</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=GSE338233</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of MIA PaCa-2 cells treated with hydroxyprogesterone caproate</name><description>Pancreatic ductal adenocarcinoma (PDAC) remains refractory to targeted therapy. This RNA-sequencing study characterizes transcriptional changes in the human PDAC cell line MIA PaCa-2 following treatment with hydroxyprogesterone caproate (HPC). Comparison with DMSO vehicle-treated cells was used to identify HPC-responsive genes and pathways. The transcriptomic analysis supported repression of cell-cycle, DNA-replication and pyrimidine-metabolism programs and contributed to investigation of the COP1-CEBPB-CDA mechanism underlying the anti-PDAC activity of HPC.</description><dates><publication>2026/07/11</publication></dates><accession>GSE338233</accession><cross_references><GSM>GSM9869673</GSM><GSM>GSM9869672</GSM><GSM>GSM9869671</GSM><GSM>GSM9869670</GSM><GSM>GSM9869679</GSM><GSM>GSM9869678</GSM><GSM>GSM9869677</GSM><GSM>GSM9869676</GSM><GSM>GSM9869675</GSM><GSM>GSM9869674</GSM><GPL>24676</GPL><GSE>338233</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>