| Literature DB >> 26825657 |
J A Guadarrama-Orozco1, A Ortega-Gómez1, E B Ruiz-García2, H Astudillo-de la Vega3, A Meneses-García4, C Lopez-Camarillo5.
Abstract
Melanoma was one of the translational cancer examples in clinic, including target therapy related to specific biomarkers impacting in the outcome of melanoma patients. Melanomagenesis involved a wide variety of mutations during his evolution; many of these mutated proteins have a kinase activity. One of the most cited proteins in melanoma is BRAF (about 50-60 % of melanomas harbors activating BRAF mutations), for these the most common is a substitution of valine to glutamic acid at codon 600 (p.V600E). Therefore, the precise identification of this underlying somatic mutation is essential; knowing the translational implications has opened a wide view of melanoma biology and therapy.Entities:
Keywords: BRAF; Inhibitor resistance; Melanoma; V600E
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Year: 2016 PMID: 26825657 DOI: 10.1007/s12094-015-1469-6
Source DB: PubMed Journal: Clin Transl Oncol ISSN: 1699-048X Impact factor: 3.405