<HashMap><database>GEO</database><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=GSE295678</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Sensory neurons drive pancreatic cancer progression through glutamatergic cancer-neuron pseudo-synapses.</name><description>The results provide significant insights into the role of Grin2D in regulating the secretion of neurotrophic factors that promote neuritogenesis. Transcriptomic analysis of orthotopically transplanted PDAC cancer cells with a knockout of the NMDA receptor subunit Grin2D, along with dorsal root ganglia (T8–T12) innervating the pancreas, strongly supports this conclusion. Furthermore, RNA-Seq analysis of tumor and ganglion biopsies from PDAC patients was performed to validate the identified gene candidates in a human context. This study tested the hypothesis that neuronal glutamate drives pancreatic cancer progression via glutamate-mediated GluN2D signaling at the cancer-neuron pseudo-synapses.</description><dates><publication>2026/06/01</publication></dates><accession>GSE295678</accession><cross_references><GSM>GSM8954989</GSM><GSM>GSM8954988</GSM><GSM>GSM8954985</GSM><GSM>GSM8954984</GSM><GSM>GSM8954987</GSM><GSM>GSM8954986</GSM><GPL>34284</GPL><GSE>295678</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>