The pleiotropic nature of NONO, a master regulator of essential biological pathways in cancers.
Domenica RonchettiValentina TrainiIlaria SilvestrisGiuseppina FabbianoFrancesco PassamontiNiccolò BolliElisa TaianaPublished in: Cancer gene therapy (2024)
NONO is a member of the Drosophila behavior/human splicing (DBHS) family of proteins. NONO is a multifunctional protein that acts as a "molecular scaffold" to carry out versatile biological activities in many aspects of gene regulation, cell proliferation, apoptosis, migration, DNA damage repair, and maintaining cellular circadian rhythm coupled to the cell cycle. Besides these physiological activities, emerging evidence strongly indicates that NONO-altered expression levels promote tumorigenesis. In addition, NONO can undergo various post-transcriptional or post-translational modifications, including alternative splicing, phosphorylation, methylation, and acetylation, whose impact on cancer remains largely to be elucidated. Overall, altered NONO expression and/or activities are a common feature in cancer. This review provides an integrated scenario of the current understanding of the molecular mechanisms and the biological processes affected by NONO in different tumor contexts, suggesting that a better elucidation of the pleiotropic functions of NONO in physiology and tumorigenesis will make it a potential therapeutic target in cancer. In this respect, due to the complex landscape of NONO activities and interactions, we highlight caveats that must be considered during experimental planning and data interpretation of NONO studies.
Keyphrases
- cell cycle
- cell proliferation
- papillary thyroid
- dna damage
- poor prognosis
- squamous cell
- oxidative stress
- gene expression
- dna methylation
- machine learning
- endothelial cells
- risk assessment
- childhood cancer
- squamous cell carcinoma
- drug delivery
- endoplasmic reticulum stress
- deep learning
- small molecule
- artificial intelligence
- dna repair
- signaling pathway
- genome wide
- climate change
- big data
- cell cycle arrest
- single molecule