Author/Authors :
Saito، نويسنده , , Masumichi and Gao، نويسنده , , Jie and Basso، نويسنده , , Katia and Kitagawa، نويسنده , , Yukiko and Smith، نويسنده , , Paula M. and Bhagat، نويسنده , , Govind and Pernis، نويسنده , , Alessandra and Pasqualucci، نويسنده , , Laura and Dalla-Favera، نويسنده , , Riccardo، نويسنده ,
Abstract :
Summary
L6 proto-oncogene encodes a transcriptional repressor necessary for the development of germinal centers (GCs) and directly implicated in lymphomagenesis. Post-GC development of B cells requires BCL6 downregulation, while its constitutive expression caused by chromosomal translocations leads to diffuse large B cell lymphoma (DLBCL). Herein we identify a signaling pathway that downregulates BCL6 expression in normal GC B cells and is blocked in a subset of DLBCL due to alterations in the BCL6 gene. Activation of the CD40 receptor leads to NF-κB-mediated induction of the IRF4 transcription factor, which, in turn, represses BCL6 expression by binding to its promoter region. A subset of DLBCL displays chromosomal translocations or mutations that disrupt the IRF4-responsive region in the BCL6 promoter and block its downregulation by CD40 signaling.