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Methods Mol Biol. 2013;971:1-25. doi: 10.1007/978-1-62703-269-8_1.

Origin and pathogenesis of B cell lymphomas.

Author information

1
Institute of Cell Biology (Cancer Research), Medical School, University of Duisburg-Essen, Essen, Germany.

Abstract

Immunoglobulin (Ig) gene remodeling by V(D)J recombination plays a central role in the generation of normal B cells, and somatic hypermutation and class switching of Ig genes are key processes during antigen-driven B cell differentiation. However, errors of these processes are involved in the development of B cell lymphomas. Ig locus-associated translocations of proto-oncogenes are a hallmark of many B cell malignancies. Additional transforming events include inactivating mutations in various tumor suppressor genes, and also latent infection of B cells with viruses, such as Epstein-Barr virus. Many B cell lymphomas require B cell antigen receptor expression, and in several instances chronic antigenic stimulation plays a role in sustaining tumor growth. Often, survival and proliferation signals provided by other cells in the microenvironment are a further critical factor in lymphoma development and pathophysiology. Many B cell malignancies derive from germinal center B cells, most likely because of the high proliferation rate of these cells and the high activity of mutagenic processes.

PMID:
23296955
DOI:
10.1007/978-1-62703-269-8_1
[Indexed for MEDLINE]

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