Recurrent mutations in NF-κB pathway components, KMT2D, and NOTCH1/2 in ocular adnexal MALT-type marginal zone lymphomas

Oncotarget. 2016 Sep 20;7(38):62627-62639. doi: 10.18632/oncotarget.11548.

Abstract

The pathogenesis of ocular adnexal marginal zone lymphomas of mucosa-associated lymphatic tissue-type (OAML) is still poorly understood. We analyzed 63 cases of such lymphomas for non-synonymous mutations in 24 candidate genes by amplicon sequencing. We validated frequent mutations in the NF-κB regulators MYD88, TNFAIP3 and TNIP1 in OAML, but also identified recurrent mutations in several additional components of the NF-κB pathway, including BCL10 and NFKBIA. Overall, 60% of cases had mutations in at least one component of NF-κB signaling, pointing to a central role of its genetic deregulation in OAML pathogenesis. Mutations in NOTCH1 and NOTCH2 were each found in 8% of cases, indicating a pathogenetic function of these factors in OAML. KMT2D was identified as the first epigenetic regulator with mutations in OAML, being mutated in 22% of cases. Mutations in MYD88 were associated with an inferior disease-free survival. Overall, we identified here highly recurrent genetic lesions in components of the NF-κB pathway, of NOTCH1 and NOTCH2 as well as KMT2D in OAML and thereby provide major novel insights into the pathogenesis of this B cell malignancy.

Keywords: KMT2D; MALT lymphoma; NF-κB; NOTCH; ocular adnexal lymphoma.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Alleles
  • Apoptosis
  • DNA Mutational Analysis
  • DNA-Binding Proteins / genetics*
  • Disease-Free Survival
  • Epigenesis, Genetic
  • Eye Neoplasms / genetics*
  • Female
  • Follow-Up Studies
  • Humans
  • Kaplan-Meier Estimate
  • Lymphoma, B-Cell, Marginal Zone / genetics*
  • Male
  • Middle Aged
  • Mutation
  • NF-kappa B / metabolism
  • Neoplasm Proteins / genetics*
  • Polymerase Chain Reaction
  • Receptor, Notch1 / genetics*
  • Receptor, Notch2 / genetics*
  • Signal Transduction

Substances

  • DNA-Binding Proteins
  • KMT2D protein, human
  • NF-kappa B
  • NOTCH1 protein, human
  • NOTCH2 protein, human
  • Neoplasm Proteins
  • Receptor, Notch1
  • Receptor, Notch2