<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/GSE324nnn/GSE324743/</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=GSE324743</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Hepatocytes promote liver metastasis of pancreatic cancer by providing exogenous serine</name><description>The liver is the major site of metastasis for pancreatic ductal adenocarcinoma (PDAC). In this work, we describe a mechanism wherein serine sythensis is essential for PDAC liver metastasis. To describe this, we knocked out Phgdh in mouse KPC cells and then co-cultured the cells with mouse hepatocytes. Published DOI: 10.1038/s41586-026-11051-z Date: 23 Sept 2026</description><dates><publication>2026/07/01</publication></dates><accession>GSE324743</accession><cross_references><GSM>GSM9584704</GSM><GSM>GSM9584705</GSM><GSM>GSM9584713</GSM><GSM>GSM9584702</GSM><GSM>GSM9584703</GSM><GSM>GSM9584708</GSM><GSM>GSM9584709</GSM><GSM>GSM9584706</GSM><GSM>GSM9584707</GSM><GSM>GSM9584696</GSM><GSM>GSM9584697</GSM><GSM>GSM9584694</GSM><GSM>GSM9584695</GSM><GSM>GSM9584711</GSM><GSM>GSM9584700</GSM><GSM>GSM9584701</GSM><GSM>GSM9584712</GSM><GSM>GSM9584698</GSM><GSM>GSM9584710</GSM><GSM>GSM9584699</GSM><GSM>GSM9584692</GSM><GSM>GSM9584693</GSM><GSM>GSM9584690</GSM><GSM>GSM9584691</GSM><GPL>24247</GPL><GSE>324743</GSE><taxon>Mus musculus</taxon><PMID>[42778596]</PMID><DOI>10.1038/s41586-026-11051-z</DOI></cross_references></HashMap>