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The effect of dual radiation and antiandrogen therapyt on prostate cancer cell lines [Myc-CaP]

GSE277593 Mus musculus (mouse) RNA-seq (gene expression) 12 samples Submitted 2025/10/29 Platform GPL16417
At a glance

RNA-seq (gene expression) · mouse · 12 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
Mus musculus (mouse)
Samples
12 samples: 3 × Myc_Cap_ENZ_IR vs 3 × Myc_Cap_ENZ vs 3 × Myc_Cap_IR vs 3 × Myc_Cap_MOCKGroups 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.
Summary (written by the submitters)
Immunotherapy has been effective in many cancer types, but failed in multiple clinical trials in cancers of the prostate, an organ largely influenced by androgen action. However, the prostate propensity cannot be explained by the immune suppressive activity of androgen receptor (AR) in T cells as reported recently.The OPeRATIC trial (NCT02816983) showed significantly improved outcomes in patients with oligometastatic castration-resistant prostate cancer (CRPC) treated with
Read the full summary ↓
metastasis-directed radiation (IR) and ARPI who experienced increased levels of CD8+CD11ahigh T cells in peripheral circulation. Here we report that AR pathway inhibitor (ARPI) plus radiation triggers robust anti-cancer immunity in prostate cancer from mice.
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 GSE277593_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 PRJNA1162876 and SRA study SRP533710. Searching any of these in the dataset finder brings you back here.

Study design
3 × Myc_Cap_ENZ_IR vs 3 × Myc_Cap_ENZ vs 3 × Myc_Cap_IR vs 3 × Myc_Cap_MOCK

Supports a between-group comparison across 12 samples.

How we read this: 4 replicated groups read from 12 sample titles; they account for 12 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
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