DUX4 is a common driver of immune evasion and immunotherapy failure in metastatic cancers.
Jose Mario Bello PinedaRobert K BradleyPublished in: eLife (2024)
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 1 year. Our data motivate future attempts to develop DUX4 as a biomarker and therapeutic target for checkpoint immunotherapy resistance.
Keyphrases
- poor prognosis
- transcription factor
- squamous cell carcinoma
- prostate cancer
- small cell lung cancer
- dna damage
- binding protein
- end stage renal disease
- cell cycle
- machine learning
- spinal cord injury
- newly diagnosed
- dendritic cells
- ejection fraction
- electronic health record
- cell proliferation
- free survival
- young adults
- big data
- case report
- childhood cancer