Bona Fide Tumor Suppressor Genes Hypermethylated in Melanoma: A Narrative Review

Loss-of-function events in tumor suppressor genes (TSGs) contribute to the development and progression of cutaneous malignant melanoma (CMM). Epigenetic alterations are the major mechanisms of TSG inactivation, in particular, silencing by promoter CpG-island hypermethylation. TSGs are valuable tools in diagnosis and prognosis and, possibly, in future targeted therapy. The aim of this narrative review is to outline bona fide TSGs affected by promoter CpG-island hypermethylation and their functional role in the progression of CMM. We conducted a systematic literature review to identify studies providing evidence of bona fide TSGs by cell line or animal experiments. We performed a broad first search and a gene-specific second search, supplemented by reference checking. We included studies describing bona fide TSGs in CMM with promoter CpG-island hypermethylation in which inactivating mechanisms were reported. We extracted data about protein role, pathway, experiments conducted to meet the bona fide criteria and hallmarks of cancer acquired by TSG inactivation. A total of 24 studies were included, describing 24 bona fide TSGs silenced by promoter CpG-island hypermethylation in CMM. Their effect on cell proliferation, apoptosis, growth, senescence, angiogenesis, migration, invasion or metastasis is also described. These data give further insight into the role of TSGs in the progression of CMM.

Automated summary

Loss-of-function events in tumor suppressor genes, particularly through epigenetic alterations like promoter CpG-island hypermethylation, contribute to the development and progression of cutaneous malignant melanoma. This study identified 24 bona fide tumor suppressor genes affected by promoter CpG-island hypermethylation in CMM, outlining their functional roles in processes such as cell proliferation, apoptosis, growth, senescence, angiogenesis, migration, invasion, and metastasis. These findings provide further insight into the impact of tumor suppressor genes on the progression of cutaneous malignant melanoma.