The complexity of NF-κB signaling in inflammation and cancer

被引:2721
作者
Hoesel, Bastian [1 ]
Schmid, Johannes A. [1 ]
机构
[1] Med Univ Vienna, Ctr Physiol & Pharmacol, Dept Vasc Biol & Thrombosis Res, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
NF-kappa B signaling; Cancer; Inflammation; Cooperativity; Crosstalk; GLYCOGEN-SYNTHASE KINASE-3; HUMAN COLORECTAL-CANCER; HUMAN MYELOID-LEUKEMIA; TRANSCRIPTION FACTOR; PROSTATE-CANCER; CELL-SURVIVAL; IKK-BETA; CHROMOSOMAL TRANSLOCATION; UBIQUITIN LIGASE; GENE-EXPRESSION;
D O I
10.1186/1476-4598-12-86
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The NF-kappa B family of transcription factors has an essential role in inflammation and innate immunity. Furthermore, NF-kappa B is increasingly recognized as a crucial player in many steps of cancer initiation and progression. During these latter processes NF-kappa B cooperates with multiple other signaling molecules and pathways. Prominent nodes of crosstalk are mediated by other transcription factors such as STAT3 and p53 or the ETS related gene ERG. These transcription factors either directly interact with NF-kappa B subunits or affect NF-kappa B target genes. Crosstalk can also occur through different kinases, such as GSK3-beta, p38, or PI3K, which modulate NF-kappa B transcriptional activity or affect upstream signaling pathways. Other classes of molecules that act as nodes of crosstalk are reactive oxygen species and miRNAs. In this review, we provide an overview of the most relevant modes of crosstalk and cooperativity between NF-kappa B and other signaling molecules during inflammation and cancer.
引用
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页数:15
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共 168 条
[81]   Reactive oxygen species in cancer [J].
Liou, Geou-Yarh ;
Storz, Peter .
FREE RADICAL RESEARCH, 2010, 44 (05) :479-496
[82]   MicroRNAs in NF-κB signaling [J].
Ma, Xiaodong ;
Buscaglia, Lindsey E. Becker ;
Barker, Juanita R. ;
Li, Yong .
JOURNAL OF MOLECULAR CELL BIOLOGY, 2011, 3 (03) :159-166
[83]   MAP3K-related kinase involved in NF-kappa B induction by TNF, CD95 and IL-1 [J].
Malinin, NL ;
Boldin, MP ;
Kovalenko, AV ;
Wallach, D .
NATURE, 1997, 385 (6616) :540-544
[84]   Cancer-related inflammation [J].
Mantovani, Alberto ;
Allavena, Paola ;
Sica, Antonio ;
Balkwill, Frances .
NATURE, 2008, 454 (7203) :436-444
[85]   RelB forms transcriptionally inactive complexes with RelA/p65 [J].
Marienfeld, R ;
May, MJ ;
Berberich, I ;
Serfling, E ;
Ghosh, S ;
Neumann, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (22) :19852-19860
[86]   Inducible phosphorylation of NF-κB p65 at serine 468 by T cell costimulation is mediated by IKKε [J].
Mattioli, I ;
Geng, H ;
Sebald, A ;
Hodel, M ;
Bucher, C ;
Kracht, M ;
Schmitz, ML .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (10) :6175-6183
[87]   Signal transduction through NF-κB [J].
May, MJ ;
Ghosh, S .
IMMUNOLOGY TODAY, 1998, 19 (02) :80-88
[88]   Rel/NF-kappa B and I kappa B proteins: an overview [J].
May, MJ ;
Ghosh, S .
SEMINARS IN CANCER BIOLOGY, 1997, 8 (02) :63-73
[89]   Inhibition of glycogen synthase kinase-3 represses androgen receptor activity and prostate cancer cell growth [J].
Mazor, M ;
Kawano, Y ;
Zhu, HN ;
Waxman, J ;
Kypta, RM .
ONCOGENE, 2004, 23 (47) :7882-7892
[90]   Mechanisms of proteasome inhibitor action and resistance in cancer [J].
McConkey, David J. ;
Zhu, Keyi .
DRUG RESISTANCE UPDATES, 2008, 11 (4-5) :164-179