<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/GSE324997/</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=GSE324997</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, 2.</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.</description><dates><publication>2026/07/28</publication></dates><accession>GSE324997</accession><cross_references><GSM>GSM9590343</GSM><GSM>GSM9590344</GSM><GSM>GSM9590352</GSM><GSM>GSM9590341</GSM><GSM>GSM9590342</GSM><GSM>GSM9590350</GSM><GSM>GSM9590340</GSM><GSM>GSM9590349</GSM><GSM>GSM9590338</GSM><GSM>GSM9590339</GSM><GSM>GSM9590347</GSM><GSM>GSM9590336</GSM><GSM>GSM9590348</GSM><GSM>GSM9590337</GSM><GSM>GSM9590345</GSM><GSM>GSM9590346</GSM><GPL>24247</GPL><GSE>324997</GSE><taxon>Mus musculus</taxon><PMID>[42778596]</PMID></cross_references></HashMap>