<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/GSE302nnn/GSE302775/</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=GSE302775</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>FABP4 binding cancer cells exhibit an invasive phenotype via PKC-mitoROS signaling</name><description>Using several high-fat diet-induced murine obesity models, we demonstrate that obesity promotes breast cancer lung metastasis through elevated levels of adipocyte-derived circulating FABP4. Circulating FABP4 directly binds to a subset of breast cancer cells via the membrane lipid PIP2. This FABP4/PIP2 interaction activates PKC signaling and enhances mitochondrial ROS production, driving cancer cell migration. these findings identify circulating FABP4 as a critical mediator of obesity-driven metastasis and highlight it as a promising therapeutic target for treating metastatic breast cancer.</description><dates><publication>2026/06/17</publication></dates><accession>GSE302775</accession><cross_references><GSM>GSM9111095</GSM><GSM>GSM9111099</GSM><GSM>GSM9111098</GSM><GSM>GSM9111097</GSM><GSM>GSM9111096</GSM><GSM>GSM9111100</GSM><GPL>24676</GPL><GSE>302775</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>