<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/GSE325nnn/GSE325047/</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=GSE325047</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Pervasive Enhanced Transcription in Inflammatory Breast Cancer Tumors and PBMCs Impacts RNA Splicing and Intronic RNAs in Plasma</name><description>Inflammatory breast cancer (IBC), the most aggressive and lethal breast cancer subtype, lacks unequivocal genomic differences or robust biomarkers that differentiate it from non-IBC. Here, Thermostable Group II Intron Reverse Transcriptase sequencing of RNA samples revealed myriad differences in tumors, PBMCs, and plasma that distinguished IBC from non-IBC patients and healthy donors across all tested non-IBC subtypes. By mapping reads to genome and transcriptome reference sequences and quantitating intron-to-exon read depth ratios, we developed methods for parallel analysis of transcriptional and post-transcriptional gene regulation. This analysis identified numerous protein-coding genes in IBC patient tumors and PBMCs with high intron-to-exon read depths, suggesting rate-limiting RNA splicing that negatively impacts mRNA production. Mirroring gene expression differences in tumors and PBMCs, over-represented protein-coding gene RNAs in IBC patient plasma were largely intron RNA fragments, while those in non-IBC patient and healthy donor plasma were largely mRNA fragments. Our findings provide new insights into IBC and should enable monitoring disease progression by liquid biopsy.</description><dates><publication>2026/05/01</publication></dates><accession>GSE325047</accession><cross_references><GSM>GSM9594650</GSM><GSM>GSM9594651</GSM><GSM>GSM9594652</GSM><GSM>GSM9594653</GSM><GSM>GSM9594654</GSM><GSM>GSM9594655</GSM><GSM>GSM9594612</GSM><GSM>GSM9594656</GSM><GSM>GSM9594690</GSM><GSM>GSM9594691</GSM><GSM>GSM9594646</GSM><GSM>GSM9594647</GSM><GSM>GSM9594648</GSM><GSM>GSM9594649</GSM><GSM>GSM9594682</GSM><GSM>GSM9594683</GSM><GSM>GSM9594640</GSM><GSM>GSM9594684</GSM><GSM>GSM9594641</GSM><GSM>GSM9594685</GSM><GSM>GSM9594686</GSM><GSM>GSM9594642</GSM><GSM>GSM9594643</GSM><GSM>GSM9594687</GSM><GSM>GSM9594644</GSM><GSM>GSM9594688</GSM><GSM>GSM9594689</GSM><GSM>GSM9594645</GSM><GSM>GSM9594680</GSM><GSM>GSM9594681</GSM><GSM>GSM9594635</GSM><GSM>GSM9594679</GSM><GSM>GSM9594636</GSM><GSM>GSM9594637</GSM><GSM>GSM9594638</GSM><GSM>GSM9594639</GSM><GSM>GSM9594671</GSM><GSM>GSM9594672</GSM><GSM>GSM9594673</GSM><GSM>GSM9594674</GSM><GSM>GSM9594630</GSM><GSM>GSM9594631</GSM><GSM>GSM9594675</GSM><GSM>GSM9594632</GSM><GSM>GSM9594676</GSM><GSM>GSM9594677</GSM><GSM>GSM9594633</GSM><GSM>GSM9594634</GSM><GSM>GSM9594678</GSM><GSM>GSM9594670</GSM><GSM>GSM9594624</GSM><GSM>GSM9594668</GSM><GSM>GSM9594669</GSM><GSM>GSM9594625</GSM><GSM>GSM9594626</GSM><GSM>GSM9594627</GSM><GSM>GSM9594628</GSM><GSM>GSM9594629</GSM><GSM>GSM9594660</GSM><GSM>GSM9594661</GSM><GSM>GSM9594662</GSM><GSM>GSM9594663</GSM><GSM>GSM9594620</GSM><GSM>GSM9594664</GSM><GSM>GSM9594621</GSM><GSM>GSM9594665</GSM><GSM>GSM9594666</GSM><GSM>GSM9594622</GSM><GSM>GSM9594623</GSM><GSM>GSM9594667</GSM><GSM>GSM9594657</GSM><GSM>GSM9594613</GSM><GSM>GSM9594614</GSM><GSM>GSM9594658</GSM><GSM>GSM9594615</GSM><GSM>GSM9594659</GSM><GSM>GSM9594616</GSM><GSM>GSM9594617</GSM><GSM>GSM9594618</GSM><GSM>GSM9594619</GSM><GPL>18573</GPL><GSE>325047</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>