<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/GSE332nnn/GSE332663/</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=GSE332663</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of Cosmc-silenced Tn+ 4T1 cells-bearing triple-negative tumors in mice</name><description>Aberrant O-glycosylation and accumulation of the Tn antigen are associated with aggressive phenotypes in triple-negative breast cancer (TNBC). To investigate the transcriptomic consequences of Tn antigen expression, we analyzed gene expression profiles of murine 4T1 breast cancer cells carrying CRISPR/Cas9-mediated silencing of the Cosmc gene (Tn+) compared with parental wild-type 4T1 cells (WT). Total RNA was extracted from 4T1 cells-bearing tumors from mice (Tn and WT)s and subjected to RNA sequencing using Illumina NovaSeq X technology.</description><dates><publication>2026/06/10</publication></dates><accession>GSE332663</accession><cross_references><GSM>GSM9752202</GSM><GSM>GSM9752203</GSM><GSM>GSM9752204</GSM><GSM>GSM9752205</GSM><GSM>GSM9752206</GSM><GSM>GSM9752195</GSM><GSM>GSM9752196</GSM><GSM>GSM9752197</GSM><GSM>GSM9752198</GSM><GSM>GSM9752199</GSM><GSM>GSM9752200</GSM><GSM>GSM9752201</GSM><GPL>34328</GPL><GSE>332663</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>