Clinical resistance associated with a novel MAP2K1 mutation in a patient with Langerhans cell histiocytosis
Year: 2018
Type: article
Study design: Case Report
Abstract: Patients with Langerhans cell histiocytosis (LCH) harbor BRAF V600E and activating mutations of MAP2K1/MEK1 in 50% and 25% of cases, respectively. We evaluated a patient with treatment-refractory LCH for mutations in the RAS-RAF-MEK-ERK pathway and identified a novel mutation in the MAP2K1 gene resulting in a p.L98_K104 > Q deletion and predicted to be auto-activating. During treatment with the MEK inhibitor trametinib, the patient's disease showed significant progression. In vitro characterization of the MAP2K1 p.L98_K104 > Q deletion confirmed its effect on cellular activation of the ERK pathway and drug resistance.
Source: Pediatric Blood & Cancer
DOI: 10.1002/pbc.27237
Authors: David O. Azorsa, David W. Lee, Daniel H. Wai, Ranjan Bista, Apurvi R. Patel, Eiman Aleem, Michael M. Henry, Robert J. Arceci
Language: English
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
OpenAlex ID: W2804486372
