<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/GSE342nnn/GSE342455/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE342455</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of tumor-associated macrophages following pharmacological SYK inhibition in a human breast cancer co-culture model</name><description>Tumor-associated macrophages contribute to immunosuppression in breast cancer. To investigate the transcriptional effects of pharmacological SYK inhibition, primary human monocytes from three healthy donors were co-cultured with BT474 breast cancer cells for 7 days in the presence of vehicle or 0.2 µM R406. CD45-positive tumor-associated macrophages were isolated by fluorescence-activated cell sorting and analyzed by bulk RNA sequencing. The dataset enables paired analysis of R406-induced transcriptional remodeling across independent donors.</description><dates><publication>2026/08/08</publication></dates><accession>GSE342455</accession><cross_references><GSM>GSM9930993</GSM><GSM>GSM9930992</GSM><GSM>GSM9930995</GSM><GSM>GSM9930994</GSM><GSM>GSM9930991</GSM><GSM>GSM9930990</GSM><GPL>24676</GPL><GSE>342455</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>