Abstract
The extracellular signal-regulated kinase (ERK) signaling pathway is activated in Langerhans cell histiocytosis (LCH) histiocytes, but only 60% of cases carry somatic activating mutations of BRAF. To identify other genetic causes of ERK pathway activation, we performed whole exome sequencing on purified LCH cells in 3 cases. One patient with wild-type BRAF alleles in his histiocytes had compound mutations in the kinase domain of ARAF. Unlike wild-type ARAF, this mutant was a highly active mitogen-activated protein kinase kinase in vitro and was capable of transforming mouse embryo fibroblasts. Mutant ARAF activity was inhibited by vemurafenib, a BRAF inhibitor, indicating the importance of fully evaluating ERK pathway abnormalities in selecting LCH patients for targeted inhibitor therapy. © 2014 by The American Society of Hematology.
Cite
CITATION STYLE
Nelson, D. S., Quispel, W., Badalian-Very, G., Van Halteren, A. G. S., Van Bos, C. D., Bovée, J. V. M. G., … Rollins, B. J. (2014). Somatic activating ARAF mutations in Langerhans cell histiocytosis. Blood, 123(20), 3152–3155. https://doi.org/10.1182/blood-2013-06-511139
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.