<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/GSE317nnn/GSE317208/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></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=GSE317208</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Immunomodulation of the prostate tumor microenvironment following inorganic Arsenic exposure</name><description>The tumor microenvironment shapes how prostate cancer (PCa) progresses through stromal-immune interactions. We investigated how adipose-derived mesenchymal/stromal cells (ASC) and chronic inorganic arsenic (iAs) exposure jointly influence PCa by using a Ras-driven murine model. ASC-conditioned media enhanced TC2Ras viability, while iAs reversed this effect. In vivo, ASC+iAs tumors showed increased weight, altered immune infiltration, and transcriptomic remodeling, including a sustained IFN-IRF1 axis and immune checkpoint upregulation. ASC-iAs crosstalk promotes immune tolerance, revealing mechanisms by which environmental toxicants modulate cancer immunity.</description><dates><publication>2026/08/12</publication></dates><accession>GSE317208</accession><cross_references><GSM>GSM9467029</GSM><GSM>GSM9467038</GSM><GSM>GSM9467027</GSM><GSM>GSM9467028</GSM><GSM>GSM9467032</GSM><GSM>GSM9467033</GSM><GSM>GSM9467030</GSM><GSM>GSM9467031</GSM><GSM>GSM9467036</GSM><GSM>GSM9467037</GSM><GSM>GSM9467034</GSM><GSM>GSM9467035</GSM><GPL>24247</GPL><GSE>317208</GSE><taxon>Mus musculus</taxon><PMID>[41730271]</PMID></cross_references></HashMap>