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Jost, PJ; Ruland, J.
Aberrant NF-kappaB signaling in lymphoma: mechanisms, consequences, and therapeutic implications.
Blood. 2007; 109(7):2700-2707
Doi: 10.1182/blood-2006-07-025809
Web of Science
PubMed
FullText
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- Führende Autor*innen der Med Uni Graz
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Jost Philipp
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- Abstract:
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The transcription factor NF-kappaB is a tightly regulated positive mediator of T- and B-cell development, proliferation, and survival. The controlled activity of NF-kappaB is required for the coordination of physiologic immune responses. However, constitutive NF-kappaB activation can promote continuous lymphocyte proliferation and survival and has recently been recognized as a critical pathogenetic factor in lymphoma. Various molecular events lead to deregulation of NF-kappaB signaling in Hodgkin disease and a variety of T- and B-cell non-Hodgkin lymphomas either up-stream or downstream of the central IkappaB kinase. These alterations are prerequisites for lymphoma cell cycling and blockage of apoptosis. This review provides an overview of the NF-kappaB pathway and discusses the mechanisms of NF-kappaB deregulation in distinct lymphoma entities with defined aberrant pathways: Hodgkin lymphoma (HL), diffuse large B-cell lymphoma (DLBCL), mucosa-associated lymphoid tissue (MALT) lymphoma, primary effusion lymphoma (PEL), and adult T-cell lymphoma/leukemia (ATL). In addition, we summarize recent data that validates the NF-kappaB signaling pathway as an attractive therapeutic target in T- and B-cell malignancies.
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Hodgkin Disease - physiopathology
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Humans -
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Leukemia-Lymphoma, Adult T-Cell - physiopathology
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Lymphocytes - physiology
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Lymphoma - genetics
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Lymphoma - physiopathology
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Lymphoma - therapy
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Lymphoma, B-Cell - physiopathology
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Lymphoma, B-Cell, Marginal Zone - genetics
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Lymphoma, B-Cell, Marginal Zone - physiopathology
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Lymphoma, Large B-Cell, Diffuse - physiopathology
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Models, Biological -
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NF-kappa B - physiology
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Oncogene Proteins, Viral - physiology
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Prognosis -
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Signal Transduction - physiology
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Translocation, Genetic -