<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/GSE292nnn/GSE292343/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE292343</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>An analysis of gemcitabine-resistant intrahepatic cholangiocarcinoma cells</name><description>Intrahepatic cholangiocarcinoma (iCCA) is an aggressive liver bile duct cancer with a poor prognosis. For advanced iCCA patients, Gemcitabine (GEM)-based chemotherapy is the standard treatment. Since there is only a 20-30% response rate for advanced CCA patients, it is a critical issue to counteract GEM resistance (GR). We selected two GR iCCA sublines (SSP-25-GR and KKU-213-GR) from the parental cells (SSP-25 and KKU-213) to determine the transcriptome profile.</description><dates><publication>2026/09/16</publication></dates><accession>GSE292343</accession><cross_references><GSM>GSM8856993</GSM><GSM>GSM8856995</GSM><GSM>GSM8856994</GSM><GSM>GSM8856996</GSM><GPL>24676</GPL><GSE>292343</GSE><taxon>Homo sapiens</taxon><PMID>[42708082]</PMID></cross_references></HashMap>