Splicing control by PHF5A is crucial for melanoma cell survival.
Tina MeißgeierMelanie Kappelmann-FenzlSebastian StaeblerAta Jadid AhariChristian MertesJulien GagneurLisa Linck-PaulusAnja Katrin BosserhoffPublished in: Cell proliferation (2024)
Abnormalities in alternative splicing are a hallmark of cancer formation. In this study, we investigated the role of the splicing factor PHD finger protein 5A (PHF5A) in melanoma. Malignant melanoma is the deadliest form of skin cancer, and patients with a high PHF5A expression show poor overall survival. Our data revealed that an siRNA-mediated downregulation of PHF5A in different melanoma cell lines leads to massive splicing defects of different tumour-relevant genes. The loss of PHF5A results in an increased rate of apoptosis by triggering Fas- and unfolded protein response (UPR)-mediated apoptosis pathways in melanoma cells. These findings are tumour-specific because we did not observe this regulation in fibroblasts. Our study identifies a crucial role of PHF5A as driver for melanoma malignancy and the described underlying splicing network provides an interesting basis for the development of new therapeutic targets for this aggressive form of skin cancer.
Keyphrases
- skin cancer
- genome wide
- endoplasmic reticulum stress
- poor prognosis
- oxidative stress
- binding protein
- protein protein
- cell death
- dna methylation
- squamous cell carcinoma
- machine learning
- small molecule
- electronic health record
- big data
- mass spectrometry
- drug delivery
- long non coding rna
- high resolution
- artificial intelligence
- transcription factor
- extracellular matrix