Article ID Journal Published Year Pages File Type
6070313 Journal of the American Academy of Dermatology 2015 11 Pages PDF
Abstract
The nevi associated with BRAF inhibitor therapy invariably lack BRAFV600E mutation. BRAF inhibition appears to cause an increased cytotoxic T-cell response and increased mitogen-activated protein kinase activity in BRAF wild-type lesions, supported by pERK expression, possibly resulting in an activated phenotype characterized by increased melanin pigmentation and deep HMB-45 expression.
Related Topics
Health Sciences Medicine and Dentistry Dermatology
Authors
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