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Exploring MicroRNA Patterns as Biomarkers of FOLFOX Chemotherapy-Induced Peripheral Neuropathy in Patients with Colorectal Cancer

GSE260661 Homo sapiens (human) RNA-seq (gene expression) 16 samples Submitted 2024/03/06 Platform GPL21697
At a glance

RNA-seq (gene expression) · human · 16 samples

What it is
RNA-seq (gene expression)Gene activity measured by sequencing. The summary does not mention single-cell work, so this is most likely bulk: one average per sample, the usual starting point for comparing groups.
Organism
Homo sapiens (human)
Topic
Colorectal cancerThis series is part of our curated briefing on it.
Samples
16 samples: 7 × Plasma, FOLFOX 7 cycles & grade 2, Day0, sample vs 3 × Plasma, FOLFOX 2 cycles & grade 1, Day0, sample vs 3 × Plasma, FOLFOX 3 cycles & grade 1, Day0, sample vs 2 × Plasma, FOLFOX 3 cycles & grade 2, Day0, sampleGroups 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
Exploring microRNA patterns as biomarkers of FOLFOX chemotherapy-induced peripheral neuropathy in patients with colorectal cancerBiochimica et biophysica acta. Molecular basis of disease · 2024
Summary (written by the submitters)
This study aimed to identify potential miRNA-based biomarkers that can predict FOLFOX-CIPN symptoms. High throughput microRNA sequencing was performed on the RNA circulating in the plasma of eight patients with CRC who underwent FOLFOX chemotherapy. miRNA expression profiles were evaluated according to two groups: those who underwent ≤three cycles and those who underwent ≥six cycles of FOLFOX chemotherapy.
Published in
Exploring microRNA patterns as biomarkers of FOLFOX chemotherapy-induced peripheral neuropathy in patients with colorectal cancer
Ju Y, Baek DH, Choi GE et al. · Biochimica et biophysica acta. Molecular basis of disease 2024 · PMID 38701955 · doi:10.1016/j.bbadis.2024.167209
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 GSE260661_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: For RNA-seq the counts are usually a table among the supplementary files (look for 'counts', 'expression', 'FPKM' or 'TPM' in the file name). The series matrix of a sequencing study is sometimes nearly empty.

Also filed as BioProject PRJNA1082637 and SRA study SRP492792. Searching any of these in the dataset finder brings you back here.

Study design
7 × Plasma, FOLFOX 7 cycles & grade 2, Day0, sample vs 3 × Plasma, FOLFOX 2 cycles & grade 1, Day0, sample vs 3 × Plasma, FOLFOX 3 cycles & grade 1, Day0, sample vs 2 × Plasma, FOLFOX 3 cycles & grade 2, Day0, sample

Supports a between-group comparison across 15 samples.

How we read this: 4 replicated groups read from 16 sample titles; they account for 15 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
More Colorectal cancer datasets

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