The endless complexity of lymphocyte differentiation and lymphomagenesis: IRF-4 downregulates BCL6 expression

Cancer Cell. 2007 Sep;12(3):189-91. doi: 10.1016/j.ccr.2007.08.012.

Abstract

The BCL6 gene is a key factor necessary for formation of germinal centers and is implicated in pathogenesis of diffuse large B cell lymphoma (DLBCL). In this issue of Cancer Cell, Saito and colleagues explore regulation of BCL6 gene expression by CD40-NF-kappaB signaling pathway and show that the IRF4 transcriptional factor, induced by the NF-kappaB canonical pathway, directly downregulates BCL6 expression. The authors further demonstrate that this negative regulatory mechanism may be disturbed in DLBCLs harboring BCL6 gene translocations or mutations. These finding suggest that IRF4 may function as a key regulator of germinal center reaction and a guardian of lymphomagenesis.

Publication types

  • Comment

MeSH terms

  • B-Lymphocytes / immunology*
  • CD40 Antigens / metabolism
  • Cell Differentiation
  • DNA-Binding Proteins / genetics*
  • Down-Regulation*
  • Germinal Center / immunology
  • Humans
  • Interferon Regulatory Factors / genetics
  • Interferon Regulatory Factors / metabolism
  • Interferon Regulatory Factors / physiology*
  • Lymphoma, B-Cell / genetics*
  • Lymphoma, Large B-Cell, Diffuse / genetics*
  • Models, Genetic
  • Mutation
  • NF-kappa B / metabolism
  • Proto-Oncogene Proteins c-bcl-6
  • Signal Transduction
  • Translocation, Genetic

Substances

  • BCL6 protein, human
  • CD40 Antigens
  • DNA-Binding Proteins
  • Interferon Regulatory Factors
  • NF-kappa B
  • Proto-Oncogene Proteins c-bcl-6
  • interferon regulatory factor-4