<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/GSE345nnn/GSE345749/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Rattus norvegicus</species><gds_type>Expression profiling by array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE345749</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of CCL2-high and CCL2-low glioma cell states</name><description>Glioma cells can reversibly occupy cellular states with distinct contributions to tumor growth and microenvironmental remodelling. To define transcriptional programmes associated with endogenous Ccl2 activity, CCL2-high and CCL2-low cells were isolated from endogenous Ccl2 reporter cells by fluorescence-activated cell sorting and analysed using one-colour gene-expression microarrays. The resulting profiles were used to identify genes and pathways preferentially represented in the CCL2-high niche-remodelling state or the CCL2-low proliferative state.</description><dates><publication>2026/09/06</publication></dates><accession>GSE345749</accession><cross_references><GSM>GSM10015922</GSM><GSM>GSM10015921</GSM><GPL>22740</GPL><GSE>345749</GSE><taxon>Rattus norvegicus</taxon></cross_references></HashMap>