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Article Abstract
Cutaneous melanoma (CM), with a continuously rising incidence worldwide, represents the most aggressive type of skin cancer, and it leads to the majority of skin cancer-related deaths. Approximately 50% of CM carry the activating BRAF mutation and, although BRAF inhibitors have demonstrated clinical efficacy, most patients often develop early resistance to treatment. Aberrant expression of non-coding RNAs (ncRNAs), which represent less than 2% of the entire transcriptome, has been implicated in CM development and progression. By using BRAF-mutant CM in vitro and in vivo models, we have recently demonstrated that the loss of Spry1 expression impairs BRAF-mutant CM progression. Therefore, the extensive long and small ncRNA datasets generated in this study might represent a valuable resource for the characterization of their roles in BRAF-mutant CM initiation and progression upon Spry1 loss, thus providing a comprehensive resource to support future studies on BRAF-mutant CM.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12405587 | PMC |
| http://dx.doi.org/10.1038/s41597-025-05807-x | DOI Listing |
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