<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/GSE291nnn/GSE291816/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></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=GSE291816</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Aberrant brain-type neuronal programs in large-cell pancreatic neuroendocrine carcinoma</name><description>High-grade pancreatic neuroendocrine carcinoma (panNEC) is a rare, aggressive cancer with limited tissue availability. Single-nucleus transcriptomics of five large-cell panNECs revealed two interesting neuroendocrine cell states: one highly proliferative with an aberrant brain-specific neuronal differentiation program and another stress-responsive state enriched for heat stress, hypoxia, and glycolysis. Our findings suggest potential therapeutic vulnerabilities, highlighting the need to evaluate the efficacy of combination therapies.</description><dates><publication>2026/05/05</publication></dates><accession>GSE291816</accession><cross_references><GSM>GSM8842822</GSM><GSM>GSM8842821</GSM><GSM>GSM8842823</GSM><GSM>GSM8842819</GSM><GSM>GSM8842818</GSM><GSM>GSM8842820</GSM><GPL>24676</GPL><GSE>291816</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>