DUX4 is a common driver of immune evasion and immunotherapy failure in metastatic cancers.
Jose Mario Bello PinedaRobert K BradleyPublished in: bioRxiv : the preprint server for biology (2023)
Cancer immune evasion contributes to checkpoint immunotherapy failure in many patients with metastatic cancers. The embryonic transcription factor DUX4 was recently characterized as a suppressor of interferon-γ signaling and antigen presentation that is aberrantly expressed in a small subset of primary tumors. Here, we report that DUX4 expression is a common feature of metastatic tumors, with ∼10-50% of advanced bladder, breast, kidney, prostate, and skin cancers expressing DUX4 . DUX4 expression is significantly associated with immune cell exclusion and decreased objective response to PD-L1 blockade in a large cohort of urothelial carcinoma patients. DUX4 expression is a significant predictor of survival even after accounting for tumor mutational burden and other molecular and clinical features in this cohort, with DUX4 expression associated with a median reduction in survival of over one year. Our data motivate future attempts to develop DUX4 as a biomarker and therapeutic target for checkpoint immunotherapy resistance.
Keyphrases
- poor prognosis
- transcription factor
- small cell lung cancer
- dna damage
- squamous cell carcinoma
- prostate cancer
- end stage renal disease
- binding protein
- cell cycle
- ejection fraction
- long non coding rna
- chronic kidney disease
- prognostic factors
- electronic health record
- dendritic cells
- risk factors
- soft tissue
- dna binding
- patient reported outcomes
- patient reported