GEOapplication/xmlftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE331nnn/GSE331309/primaryOK200TranscriptomicsHomo sapiensExpression profiling by high throughput sequencinghttps://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE331309GEOGSEfalseTranscriptional profiling of necroptotic signalling in IFNγ/TNF-treated human colonocyte organoids with BCL2-mediated apoptosis blockadeThis bulk RNA-seq experiment was designed to investigate the contribution of necroptotic signalling to the inflammatory transcriptional response of human intestinal epithelial cells. Patient-derived human intestinal organoids from four independent donors were differentiated into colonocyte-enriched organoids and engineered to overexpress BCL2, thereby limiting apoptosis-associated cell death. Organoids were then exposed to IFNγ and TNF to model an inflammatory cytokine environment relevant to intestinal inflammation, in the presence or absence of pharmacological inhibitors targeting necroptotic signalling. Transcriptomic profiling was performed to determine how inhibition of necroptosis-associated pathways alters epithelial inflammatory responses under conditions where apoptosis is blocked. This dataset enables comparison of cytokine-induced gene expression programs across donor-derived organoids and inhibitor-treated conditions, providing insight into the role of necroptotic signalling in shaping epithelial responses to IFNγ/TNF-driven inflammation.2026/09/03GSE331309GSM9743669GSM9743679GSM9743678GSM9743677GSM9743683GSM9743672GSM9743671GSM9743682GSM9743681GSM9743670GSM9743680GSM9743676GSM9743675GSM9743674GSM9743684GSM974367330173331309Homo sapiens[42658927]