A signaling pathway mediating downregulation of BCL6 in germinal center B cells is blocked by BCL6 gene alterations in B cell lymphoma

被引:296
作者
Saito, Masumichi
Gao, Jie
Basso, Katia
Kitagawa, Yukiko
Smith, Paula M.
Bhagat, Govind
Pernis, Alessandra
Pasqualucci, Laura
Dalla-Favera, Riccardo [1 ]
机构
[1] Columbia Univ, Herbert Irving Comprehens Canc Ctr, Inst Canc Genet, New York, NY 10032 USA
[2] Columbia Univ, Dept Pathol, New York, NY 10032 USA
[3] Columbia Univ, Dept Med, New York, NY 10032 USA
[4] Columbia Univ, Dept Genet & Dev, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.ccr.2007.08.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The BCL6 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-kappa B-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.
引用
收藏
页码:280 / 292
页数:13
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