Treatment of Cutaneous Melanoma Harboring SMO p.Gln216Arg Mutation with Imiquimod: An Old Drug with New Results.
Teresa TroianiStefania NapolitanoGabriella BrancaccioValentina BelliAnnarita NappiCaterina MiroDomenico SalvatoreMonica DenticeMichele CaragliaRenato FrancoEmilio Francesco GiuntaVincenzo De FalcoDavide CiardielloFortunato CiardielloGiuseppe ArgenzianoPublished in: Journal of personalized medicine (2021)
Melanoma is the most lethal form of skin cancer and its incidence is growing worldwide. In the last ten years, the therapeutic scenario of this disease has been revolutionized by the introduction of targeted therapies and immune-checkpoint inhibitors. However, in patients with many lesions and bulky tumors, in which surgery is no longer feasible, there is a need for new treatment options. Here we report, for the first time to our knowledge, a clinical case where a melanoma patient harboring the SMO p.Gln216Arg mutation has been treated with imiquimod, showing a complete and durable response. To better explain this outstanding response to the treatment, we transfected a melanoma cell line (MeWo) with the SMO p.Gln216Arg mutation in order to evaluate its role in response to the imiquimod treatment. Moreover, to better demonstrate that the antitumor activity of imiquimod was due to its role in suppressing the oncogenic SMO signaling pathway, independently of its immune modulating function, an in vivo experiment has been performed. This clinical case opens up a new scenario for the treatment of melanoma patients identifying a new potentially druggable target.
Keyphrases
- skin cancer
- signaling pathway
- end stage renal disease
- healthcare
- chronic kidney disease
- emergency department
- transcription factor
- coronary artery disease
- acute coronary syndrome
- cell proliferation
- prognostic factors
- case report
- basal cell carcinoma
- smoking cessation
- peritoneal dialysis
- replacement therapy
- patient reported