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Chromatin profiling following FASN knockdown in UMUC3 bladder cancer cell lines treated under cigarette smoke media and regular media conditions.

GSE308925 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 12 samples Submitted 2026/06/11 Platform GPL21697
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 12 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
Bladder cancerThis series is part of our curated briefing on it.
Samples
12 samples
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
Cigarette smoke induces FASN-dependent fatty acid metabolic rewiring to drive bladder cancer progressionCancer letters · 2026
Summary (written by the submitters)
To assess the genome-wide chromatin effect of FASN knockdown under cigarette smoke treated conditions in UMUC3 bladder cancer cell lines. ChIP-seq was performed by pulling down with H3K18Ac antibody in Control and FASN KD cells upon 10%CSM treatment.
Published in
Cigarette smoke induces FASN-dependent fatty acid metabolic rewiring to drive bladder cancer progression
Amara CS, Piyarathna DWB, Kamal AHM et al. · Cancer letters 2026 · PMID 42092682 · doi:10.1016/j.canlet.2026.218562
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 GSE308925_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 PRJNA1333416 and SRA study SRP625555. Searching any of these in the dataset finder brings you back here.

Samples in this study

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