An Analysis of JADE2 in Non-Small Cell Lung Cancer (NSCLC).
Ciara MurphyGlòria Gornés PonsAnna KeoghLisa RyanLorraine McCarraChris Maria JoseShagun KesarSiobhan NicholsonGerard J FitzmauriceRonan RyanVincent YoungSinead CuffeStephen P FinnSteven G GrayPublished in: Biomedicines (2023)
The JADE family comprises three members encoded by individual genes and roles for these proteins have been identified in chromatin remodeling, cell cycle progression, cell regeneration and the DNA damage response. JADE family members, and in particular JADE2 have not been studied in any great detail in cancer. Using a series of standard biological and bioinformatics approaches we investigated JADE2 expression in surgically resected non-small cell lung cancer (NSCLC) for both mRNA and protein to examine for correlations between JADE2 expression and overall survival. Additional correlations were identified using bioinformatic analyses on multiple online datasets. Our analysis demonstrates that JADE2 expression is significantly altered in NSCLC. High expression of JADE2 is associated with a better 5-year overall survival. Links between JADE2 mRNA expression and a number of mutated genes were identified, and associations between JADE2 expression and tumor mutational burden and immune cell infiltration were explored. Potential new drugs that can target JADE2 were identified. The results of this biomarker-driven study suggest that JADE2 may have potential clinical utility in the diagnosis, prognosis and stratification of patients into various therapeutically targetable options.
Keyphrases
- poor prognosis
- small cell lung cancer
- binding protein
- dna damage response
- stem cells
- end stage renal disease
- genome wide
- gene expression
- cell proliferation
- squamous cell carcinoma
- social media
- transcription factor
- chronic kidney disease
- dna damage
- advanced non small cell lung cancer
- mesenchymal stem cells
- healthcare
- risk factors
- single cell
- peritoneal dialysis
- bone marrow
- cell therapy
- health information
- papillary thyroid
- tyrosine kinase
- epidermal growth factor receptor
- oxidative stress
- bioinformatics analysis
- squamous cell