GEOapplication/xmlftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE335nnn/GSE335441/primaryOK200TranscriptomicsHomo sapiensExpression profiling by high throughput sequencinghttps://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE335441GEOGSEfalseHCFC2 knockdown in human colorectal cancer cell linesThere is an urgent and unmet need for improved therapeutic approaches against aggressive colorectal cancer (CRC). Host Cell Factor 2 (HCF-2) is a transcriptional coactivator with an emerging role in cancer biology. Our data suggest that HCF-2 is a critical effector of peroxisome proliferator-activated receptor-gamma coactivator 1 beta (PGC-1β) signaling in CRC, supporting its potential as a targetable vulnerability in aggressive disease. Previous findings from our lab show that shRNA-mediated depletion of HCF-2 decreases anchorage-independent growth in CRC models, indicating a role for HCF-2 in CRC cell survival. To identify transcriptional programs regulated downstream of HCF-2, we performed RNA-seq following shRNA-mediated HCF-2 knockdown in SW620 and T84 CRC cell lines. Knockdown efficiency was confirmed by western blot prior to sample submission, and RNA-seq data were provided to collaborators for downstream computational analysis. The resulting transcriptomic profile will help define HCF-2-dependent gene expression programs and potential targetable vulnerabilities in aggressive CRC.2026/06/15GSE335441GSM9813832GSM9813831GSM9813842GSM9813834GSM9813833GSM9813841GSM9813830GSM9813840GSM9813829GSM9813828GSM9813839GSM9813825GSM9813836GSM9813835GSM9813838GSM9813827GSM9813826GSM981383734281335441Homo sapiens