Mutations of MAP2K1 are frequent in pediatric-type follicular lymphoma and result in ERK pathway activation

Author:

Schmidt Janine1,Ramis-Zaldivar Joan Enric2ORCID,Nadeu Ferran2ORCID,Gonzalez-Farre Blanca2ORCID,Navarro Alba2ORCID,Egan Caoimhe3,Montes-Mojarro Ivonne Aidee1,Marafioti Teresa4,Cabeçadas Jose5,van der Walt Jon6,Dojcinov Stefan7,Rosenwald Andreas89,Ott German1011,Bonzheim Irina1,Fend Falko1,Campo Elias2ORCID,Jaffe Elaine S.3,Salaverria Itziar2ORCID,Quintanilla-Martinez Leticia1ORCID

Affiliation:

1. Institute of Pathology and Neuropathology, Eberhard Karls University of Tübingen and Comprehensive Cancer Center, Tübingen University Hospital, Tübingen, Germany;

2. Hematopathology Unit, Hospital Clinic, Institut d’Investigacions Biomèdiques August Pi Sunyer, Centro de Investigación Biomédica en Red de Cáncer, Barcelona, Spain;

3. Hematopathology Section, Laboratory of Pathology, National Cancer Institute, Bethesda, MD;

4. Department of Cellular Pathology, Barts and The London National Health Service Trust, London, United Kingdom;

5. Pathology Department, Instituto Portugues de Oncología, Lisbon, Portugal;

6. Department of Histopathology, Guy's and St Thomas’ Hospitals, London, United Kingdom;

7. Department of Pathology, All Wales Lymphoma Panel, University Hospital of Wales, Cardiff, United Kingdom;

8. Institute of Pathology, University of Würzburg, Würzburg, Germany;

9. Comprehensive Cancer Center Mainfranken, Würzburg, Germany;

10. Department of Clinical Pathology, Robert Bosch Hospital, Stuttgart, Germany; and

11. Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany

Abstract

Key Points TNFRSF14 and MAP2K1 mutations are frequent in PTFL but do not occur together in the majority of cases. MAP2K1 mutations lead to activation of the downstream target phosphorylated extracellular signal-regulated kinase.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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