<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/GSE304nnn/GSE304220/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE304220</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Cancer cachexia induces senescent reprogramming of brown adipose tissue and pro-cachectic S100A9 secretion by adipocytes</name><description>Cancer-associated cachexia (CAC) is a multifactorial wasting syndrome characterized by the progressive loss of fat and lean mass, systemic inflammation, and poor therapeutic responsiveness. While brown adipose tissue (BAT) is traditionally considered a protective, energy-dissipating organ, its qualitative remodelling in CAC remains poorly characterized.</description><dates><publication>2026/06/25</publication></dates><accession>GSE304220</accession><cross_references><GSM>GSM9145404</GSM><GSM>GSM9145403</GSM><GSM>GSM9145402</GSM><GSM>GSM9145401</GSM><GSM>GSM9145400</GSM><GSM>GSM9145399</GSM><GSM>GSM9145398</GSM><GSM>GSM9145397</GSM><GPL>24247</GPL><GSE>304220</GSE><taxon>Mus musculus</taxon><PMID>[42069727]</PMID></cross_references></HashMap>