<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/GSE287nnn/GSE287930/</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=GSE287930</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Epigenetic modulation of polyamine biosynthetic pathways rectifies T cell dysfunction to enhance anti-tumor immunity in lung cancer</name><description>T cell exhaustion (TEX) represents a critical target for immunotherapy in cancer. Nevertheless, T cells exhibit diminished responsiveness to immune checkpoint inhibitors once they transition to a terminally-exhausted state. In this study, we employed Single-cell RNA-seq to demonstrate BETis reduced terminal TEX while promoting progenitor TEX through activation of the MYC-ODC axis.</description><dates><publication>2026/04/06</publication></dates><accession>GSE287930</accession><cross_references><GSM>GSM8755610</GSM><GSM>GSM8755611</GSM><GPL>24676</GPL><GSE>287930</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>