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BRAF G596R mutation in a slow-progressing melanoma
Journal article   Open access   Peer reviewed

BRAF G596R mutation in a slow-progressing melanoma

Deqin Ma and Ling Gao
Pathology and laboratory medicine international, Vol.7(default), pp.63-66
08/2015
DOI: 10.2147/PLMI.S88369
url
https://doi.org/10.2147/PLMI.S88369View
Published (Version of record) Open Access

Abstract

More than 50% of melanomas harbor a single V600E point mutation in the kinase domain of the BRAF gene, resulting in constitutive activation of the MAP kinase pathway. The kinase loop in BRAF begins with Asp-Phe-Gly (DFG; codons 594–596). Mutations in this region are rare, and the effect on tumorigenesis or progression is unknown. We present a slow-progressing metastatic melanoma with a p.G596R (c.1786G>C) mutation in an 84-year-old female. This mutation has only been reported in two cases of melanoma in the current literature, with no clinical information available. Mutations in the DFG motif are considered low-activating through indirect binding and allosteric activation of the CRAF protein. Our patient has carried a clinical diagnosis of melanoma for over 25 years, suggesting that the G596R mutation may be associated with her indolent clinical course. It is unknown whether patients carrying this mutation will benefit from vemurafenib therapy. Our patient declined medical treatment.

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