<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Csv>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE240nnn/GSE240703/suppl/GSE240703_all_samples_count.csv.gz</Csv><Csv>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE240nnn/GSE240703/suppl/GSE240703_all_samples_fpkm.csv.gz</Csv><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE240nnn/GSE240703/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE240703</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>The effect of Sphingosine-1-Phosphate Receptor 1 and Complement Component 3 conditional knockouts on primary tumors in MMTV-PyMT mice.</name><description>Sphingolipid metabolism has been shown to regulate intracellular complement activation via sphingosine-1-phosphate receptor 1 (S1PR1) signaling to stimulate NLRP3 inflammasome-induced cancer metastasis. Here, the transcriptomic effects of S1PR1 and complement C3 conditional knockouts on primary tumors in MMTV-PyMT Mice were assessed.</description><dates><publication>2026/08/11</publication></dates><accession>GSE240703</accession><cross_references><GSM>GSM7707650</GSM><GSM>GSM7707640</GSM><GSM>GSM7707641</GSM><GSM>GSM7707642</GSM><GSM>GSM7707643</GSM><GSM>GSM7707644</GSM><GSM>GSM7707645</GSM><GSM>GSM7707646</GSM><GSM>GSM7707647</GSM><GSM>GSM7707648</GSM><GSM>GSM7707649</GSM><GSM>GSM7707639</GSM><GPL>24247</GPL><GSE>240703</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>