<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/GSE279nnn/GSE279017/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE279017</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Spatial transcriptomic analysis of head and neck squamous cell carcinoma reveals novel regulators of hybrid epithelial-to-mesenchymal transition</name><description>Head and neck squamous cell carcinoma (HNSCC) is characterized by a high degree of intra- and inter-tumoral heterogeneity. Here we use spatial transcriptomics (ST) to profile both HPV-positive and HPV-negative HNSCC, uncovering distinct patterns of spatial organization of malignant cells and the surrounding tumor microenvironment across groups of tumors. First, we find that HPV-positive HNSCC is characterized by high cellular density in all cellular compartments with distinct expression of hypoxia, senescence, and cell cycle-associated genes in the malignant compartment. In HPV-negative HNSCC, we find two distinct spatial patterns of a partial epithelial-to-mesenchymal transition (p-EMT) program. One pattern is spatially associated with fibroblasts, characterized by p-EMT at the leading edge of tumor nests (“p-EMT edge”), and mediated by TGFB-signaling. The other pattern features high p-EMT expression in the core of tumor nests (“p-EMT core”). In p-EMT core tumors, we observe high co-localization of p-EMT cells with an inflammatory response program including neutrophils and macrophages, as well as differential expression of distinct ligands, including OSM. In vitro experiments demonstrate that OSM can induce the p-EMT state in multiple HNSCC models. Together these findings suggest that multiple p-EMT phenotypes exist across HPV-unrelated HNSCC and are mediated by distinct cell-to-cell signaling mechanisms, highlighting potential novel therapeutic vulnerabilities.</description><dates><publication>2026/06/21</publication></dates><accession>GSE279017</accession><cross_references><GSM>GSM8559688</GSM><GSM>GSM8559677</GSM><GSM>GSM8559689</GSM><GSM>GSM8559678</GSM><GSM>GSM8559679</GSM><GSM>GSM8559684</GSM><GSM>GSM8559673</GSM><GSM>GSM8559685</GSM><GSM>GSM8559674</GSM><GSM>GSM8559675</GSM><GSM>GSM8559686</GSM><GSM>GSM8559676</GSM><GSM>GSM8559687</GSM><GSM>GSM8559680</GSM><GSM>GSM8559681</GSM><GSM>GSM8559670</GSM><GSM>GSM8559682</GSM><GSM>GSM8559671</GSM><GSM>GSM8559672</GSM><GSM>GSM8559683</GSM><GPL>34295</GPL><GSE>279017</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>