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Transcriptomic and Epigenomic Profiling of MYADM and RhoA Regulatory Networks in Metastatic Cancer Models

GSE297013 Mus musculus (mouse) ChIP-seq / ATAC-seq (genome binding and open chromatin) 52 samples Submitted 2025/08/19 Platform GPL19057Platform GPL16791Platform GPL17021
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 52 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
Mus musculus (mouse)
Samples
52 samples: 22 conditions, mostly in duplicateGroups 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
MYADM Activates RhoA-Mediated Ameboid Migration to Drive MetastasisCancer research · 2025
Summary (written by the submitters)
This dataset comprises bulk RNA-seq and ATAC-seq profiles across multiple human and murine cell lines with diverse metastatic potentials to investigate the role of MYADM and RhoA in cancer progression. RNA-seq samples include MYADM and RhoA knockdown in murine breast cancer cells (4T1), MYADM overexpression in human mammary epithelial cells (MCF10A), and metastatic progression models derived from human kidney (ACHN) and lung (CL1 series) cell lines.
Read the full summary ↓
Additionally, transcriptomic data were collected from bone marrow-derived monocytes isolated from wild-type and MYADM whole-body knockout mice. ATAC-seq data were generated from selected RNA-seq matched samples to characterize chromatin accessibility changes associated with MYADM and RhoA perturbation. All cells were cultured under standard conditions. This dataset provides insights into transcriptional and epigenetic alterations during MYADM- and RhoA-mediated cancer metastasis.
Published in
MYADM Activates RhoA-Mediated Ameboid Migration to Drive Metastasis
Tsai YT, Liu ET, Yang MH et al. · Cancer research 2025 · PMID 40882023 · doi:10.1158/0008-5472.CAN-25-0006
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 GSE297013_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 PRJNA1262379 and SRA study SRP585081. Searching any of these in the dataset finder brings you back here.

Study design
22 conditions, mostly in duplicate
4T1 cells, shContral, ×3 4T1 cells, shMYADM#1, ×3 4T1 cells, shMYADM#2, ×3 4T1 cells, shRhoA, ×3 ATAC_4T1 cells, shContral, ×3 ATAC_4T1 cells, shMYADM#1, ×3 ATAC_4T1 cells, Vector, ×3 ATAC_4T1 cells, shRhoA, ×3 +14 more

Supports a case/control comparison: 4 samples read as cases, 4 as controls.

How we read this: 22 replicated groups read from 52 sample titles; they account for 52 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

+ 12 more — browse all 52 samples with per-sample file links →

Datasets on a similar topic

Search all RNA-seq 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.