<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/GSE277nnn/GSE277135/</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=GSE277135</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Characterization of tumour microenvironment landscape of mouse oral cancer tumours</name><description>Access of CD8+ T cells inside tumour nests is shaped by the tumour microenvironment (TME). Cancer-associated fibroblasts (CAFs) are among the most abundant TME components and have been associated with poor survival and T cells exclusion. However, the mechanisms that link CAFs presence with T cell blockade are unclear and there is a huge unmet medical need to increase T cell accessibility inside tumour cores. Here, we established single cell RNAseq of syngeneic murine models of head and neck squamous cell carcinoma that recapitulate different tumour-stroma organizations and evolutions (MOC1 and MOC2). MOC1 tumours are immune indolent and transition from a T cell infiltrated to an immune excluded/desert TME over time. MOC2 are more aggressive and are rich in myeloid cells while being T cell desert.</description><dates><publication>2026/09/01</publication></dates><accession>GSE277135</accession><cross_references><GSM>GSM8514897</GSM><GSM>GSM8514896</GSM><GSM>GSM8514899</GSM><GSM>GSM8514898</GSM><GSM>GSM8514901</GSM><GSM>GSM8514900</GSM><GSM>GSM8514903</GSM><GSM>GSM8514902</GSM><GSM>GSM8514904</GSM><GPL>24247</GPL><GSE>277135</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>