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p300 catalytic inhibition selectively targets IRF4 oncogenic activity in multiple myeloma

GSE307536 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 164 samples Submitted 2025/10/20 Platform GPL34284Platform GPL24676Platform GPL20301
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 164 samples

What it is
ChIP-seq / ATAC-seq (genome binding and open chromatin)Where proteins bind the genome, or which regions are open and active.
Organism
Homo sapiens (human)
Topic
Multiple myelomaThis series is part of our curated briefing on it.
Samples
164 samples: 60 conditions, mostly in triplicateGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
Catalytic Inhibition of p300 Preferentially Targets IRF4 Oncogenic Activity and Tumor Growth in Multiple MyelomaCancer research · 2026
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
Catalytic Inhibition of p300 Preferentially Targets IRF4 Oncogenic Activity and Tumor Growth in Multiple Myeloma
Lenoir WF, McKeown MR, Giorgetti G et al. · Cancer research 2026 · PMID 41248492 · doi:10.1158/0008-5472.CAN-25-3440
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE307536_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.

Also filed as BioProject PRJNA1321942 and SRA study SRP525907. Searching any of these in the dataset finder brings you back here.

Study design
60 conditions, mostly in triplicate
MM1R_siIRF4 ×3 MM1R_CTRL ×3 KMS-12-BM_siIRF4 ×3 KMS-12-BM_CTRL ×3 MM1S_siIRF4 ×3 MM1S_CTRL ×3 KMS-12-PE_siIRF4 ×3 KMS-12-PE_CTRL ×3 +58 more

Supports a between-group comparison across 158 samples.

How we read this: 60 replicated groups read from 164 sample titles; they account for 158 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study

+ 124 more — browse all 164 samples with per-sample file links →

More Multiple myeloma datasets

Search all human ChIP / ATAC / CUT&Tag datasets in GEO →

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Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.