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BCR::ABL1-induced enhancer reprogramming uncovers hypersensitivity of Ph+B-ALL cells to enhancer-targeting drugs [ChIP-Seq]

GSE279644 Homo sapiens; Mus musculus Genome binding/occupancy profiling by high throughput sequencing 91 samples Submitted 2026/02/27 Platform GPL21103Platform GPL20301
Summary
To better understand how BCR::ABL1 establishes the Ph+B-ALL-defining transcriptional program, we adopted an integrative multi-omics approach to study the transcriptome, enhancer activities, and 3-dimensional interactions of enhancers with target genes in Ph+B-ALL cells. We performed an in-depth analysis of cells from human Ph+B-ALL patients and a murine Ph+B-ALL model using ChIP-Seq, RNA-Seq, and Hi-C-based methods to link enhancers to the promoters they regulate. We further interfered with enhancer function to explore their role in Ph+B-ALL and investigated BCR::ABL1-regulated TFs that are recruited to them using targeted proteasomal degradation and RNA interference (RNAi).
Published in
BCR::ABL1-Induced Enhancer Reprogramming Uncovers Hypersensitivity of Ph+B-ALL Cells to Enhancer-Targeting Drugs
Ng HL, Glaser TL, Zhu J et al. · Advanced science (Weinheim, Baden-Wurttemberg, Germany) 2026 · PMID 41764406 · doi:10.1002/advs.202517231
This dataset
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Direct links to NCBI, no account and no request form: the whole study as GSE279644_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 91 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1173753 and SRA study SRP538975. Searching any of these in the dataset finder brings you back here.

Study design
31 conditions, each sampled once — no replicated groups
BA_p190_DMSO_H3K27ac ×3 BA_p190_PON_H3K27ac ×3 EV_D3_H3K27ac ×3 BCR_D60 ×3 EV_D7 ×2

Read from the first 40 of 91 sample titles: 31 distinct titles with little repetition. Check it against the sample list below before relying on it.

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