
Pathogenesis of Human B Cell Lymphomas
Author(s) -
Arthur L. Shaffer,
Ryan M. Young,
Louis M. Staudt
Publication year - 2012
Publication title -
annual review of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 18.301
H-Index - 301
eISSN - 1545-3278
pISSN - 0732-0582
DOI - 10.1146/annurev-immunol-020711-075027
Subject(s) - biology , epigenetics , chromatin , b cell , cancer research , pathogenesis , genetics , carcinogenesis , chromosomal translocation , signal transduction , gene , microbiology and biotechnology , immunology , antibody
The mechanisms that drive normal B cell differentiation and activation are frequently subverted by B cell lymphomas for their unlimited growth and survival. B cells are particularly prone to malignant transformation because the machinery used for antibody diversification can cause chromosomal translocations and oncogenic mutations. The advent of functional and structural genomics has greatly accelerated our understanding of oncogenic mechanisms in lymphomagenesis. The signaling pathways that normal B cells utilize to sense antigens are frequently derailed in B cell malignancies, leading to constitutive activation of prosurvival pathways. These malignancies co-opt transcriptional regulatory systems that characterize their normal B cell counterparts and frequently alter epigenetic regulators of chromatin structure and gene expression. These mechanistic insights are ushering in an era of targeted therapies for these cancers based on the principles of pathogenesis.