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- W3160737750 endingPage "5115" @default.
- W3160737750 startingPage "5115" @default.
- W3160737750 abstract "Melanoma is one of the most aggressive forms of skin cancer and is therapeutically challenging, considering its high mutation rate. Following the development of therapies to target BRAF, the most frequently found mutation in melanoma, promising therapeutic responses were observed. While mono- and combination therapies to target the MAPK cascade did induce a therapeutic response in BRAF-mutated melanomas, the development of resistance to MAPK-targeted therapies remains a challenge for a high proportion of patients. Resistance mechanisms are varied and can be categorised as intrinsic, acquired, and adaptive. RASSF1A is a tumour suppressor that plays an integral role in the maintenance of cellular homeostasis as a central signalling hub. RASSF1A tumour suppressor activity is commonly lost in melanoma, mainly by aberrant promoter hypermethylation. RASSF1A loss could be associated with several mechanisms of resistance to MAPK inhibition considering that most of the signalling pathways that RASSF1A controls are found to be altered targeted therapy resistant melanomas. Herein, we discuss resistance mechanisms in detail and the potential role for RASSF1A reactivation to re-sensitise BRAF mutant melanomas to therapy." @default.
- W3160737750 created "2021-05-24" @default.
- W3160737750 creator A5011831209 @default.
- W3160737750 creator A5088061809 @default.
- W3160737750 date "2021-05-12" @default.
- W3160737750 modified "2023-10-13" @default.
- W3160737750 title "Resistance to Targeted Therapy and RASSF1A Loss in Melanoma: What Are We Missing?" @default.
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