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Impact of CEBPβ depletion on enhancer responses to dexamethasone in Multiple Myeloma cells

GSE312300 Homo sapiens Genome binding/occupancy profiling by high throughput sequencing 12 samples 2025/12/03 GPL24676
Summary
Multiple myeloma (MM) is the second most common hematological cancer. While MM is considered treatable, it remains incurable due to the eventual drug resistance in nearly all patients. A cornerstone therapeutic for MM is dexamethasone, a synthetic glucocorticoid with anti-inflammatory and anti-myeloma properties. In this study, we investigate the role of CEBPβ in modulating enhancer activities, measured by H3K27ac, in response to dexamethasone in MM cells.
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