<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/GSE235nnn/GSE235593/</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=GSE235593</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Impact of Conditional Knockout of Complement C3 and Sphingosine-1-Phosphate Receptor 1 (S1PR1) on Lung Metastasis in MMTV-PyMT Mice</name><description>Recent evidence suggests that sphingosine-1-phosphate receptor 1 (S1PR1) modulates the intracellular complement system or the complosome to induce NLRP3 inflammasome formation and the release of IL-1β through caspase-1, thereby promoting tumor metastasis. Here, we examined the transcriptomic effects of S1PR1 and complement C3 conditional knockouts on lung metastasis in MMTV-PyMT Mice, a widely used model for studying mammary tumor progression and metastasis.</description><dates><publication>2026/06/19</publication></dates><accession>GSE235593</accession><cross_references><GSM>GSM7506003</GSM><GSM>GSM7506004</GSM><GSM>GSM7506001</GSM><GSM>GSM7506002</GSM><GSM>GSM7506000</GSM><GSM>GSM7505999</GSM><GSM>GSM7505998</GSM><GSM>GSM7506009</GSM><GSM>GSM7506007</GSM><GSM>GSM7506008</GSM><GSM>GSM7506005</GSM><GSM>GSM7506006</GSM><GPL>24247</GPL><GSE>235593</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>