Details

Autor(en) / Beteiligte

• Schmidt, Janine
• Ramis-Zaldivar, Joan Enric
• Nadeu, Ferran
• Gonzalez-Farre, Blanca
• Navarro, Alba
• Egan, Caoimhe
• Montes-Mojarro, Ivonne Aidee
• Marafioti, Teresa
• Cabeçadas, Jose
• van der Walt, Jon
• Dojcinov, Stefan
• Rosenwald, Andreas
• Ott, German
• Bonzheim, Irina
• Fend, Falko
• Campo, Elias
• Jaffe, Elaine S.
• Salaverria, Itziar
• Quintanilla-Martinez, Leticia

Titel

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

Ist Teil von

• Blood, 2017-07, Vol.130 (3), p.323-327

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2017

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Pediatric-type follicular lymphoma (PTFL) is a B-cell lymphoma with distinctive clinicopathological features. Recently, recurrent genetic alterations of potential importance for its pathogenesis that disrupt pathways associated with the germinal center reaction (TNFRSF14, IRF8), immune escape (TNFRSF14), and anti-apoptosis (MAP2K1) have been described. In an attempt to shed more light onto the pathogenesis of PTFL, an integrative analysis of these mutations was undertaken in a large cohort of 43 cases previously characterized by targeted next-generation sequencing and copy number array. Mutations in MAP2K1 were found in 49% (20/41) of the cases, second in frequency to TNFRSF14 alterations (22/41; 54%), and all together were present in 81% of the cases. Immunohistochemical analysis of the MAP2K1 downstream target extracellular signal-regulated kinase demonstrated its phosphorylation in the evaluable cases and revealed a good correlation with the allelic frequency of the MAP2K1 mutation. The IRF8 p.K66R mutation was present in 15% (6/39) of the cases and was concomitant with TNFRSF14 mutations in 4 cases. This hot spot seems to be highly characteristic for PTFL. In conclusion, TNFRSF14 and MAP2K1 mutations are the most frequent genetic alterations found in PTFL and occur independently in most cases, suggesting that both mutations might play an important role in PTFL lymphomagenesis. •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.