Cross-talk between nuclear receptors and nuclear factor κB

被引:206
作者
De Bosscher, K. [1 ]
Vanden Berghe, W. [1 ]
Haegeman, G. [1 ]
机构
[1] Univ Ghent, Dept Biol Mol, LEGEST, B-9000 Ghent, Belgium
关键词
NF-kappaB; hormone; nuclear receptor; glucocorticoid receptor; estrogen receptor; PPAR;
D O I
10.1038/sj.onc.1209935
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
A variety of studies have shown that some activated nuclear receptors (NRs), especially the glucorticoid receptor, the estrogen receptor and peroxisome proliferator-activated receptor, can inhibit the activity of the transcription factor nuclear factor kappa B (NF-kappa B), which plays a key role in the control of genes involved in inflammation, cell proliferation and apoptosis. This review describes the molecular mechanisms of cross-talk between NRs and NF-kappa B and the biological relevance of this crosstalk. The importance and mechanistic aspects of selective NR modulation are discussed. Also included are future research prospects, which will lead to a new era in the field of NR research with the aim of specifically inhibiting NF-kappa B-driven gene expression for anti-inflammatory, anti-tumor and immune-modulatory purposes.
引用
收藏
页码:6868 / 6886
页数:19
相关论文
共 252 条
[1]   CREB-binding protein in androgen receptor-mediated signaling [J].
Aarnisalo, P ;
Palvimo, JJ ;
Jänne, OA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (05) :2122-2127
[2]   NF-kappa B involvement in IL-1 beta-induction of GM-CSF and COX-2: Inhibition by glucocorticoids does not require I-kappa B. [J].
Adcock, IM ;
Newton, R ;
Barnes, PJ .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1997, 25 (02) :S154-S154
[3]   Endocrine-responsive breast cancer and strategies for combating resistance [J].
Ali, S ;
Coombes, RC .
NATURE REVIEWS CANCER, 2002, 2 (02) :101-+
[4]   Transgenic mice expressing soluble tumor necrosis factor-receptor are protected against bone loss caused by estrogen deficiency [J].
Ammann, P ;
Rizzoli, R ;
Bonjour, JP ;
Bourrin, S ;
Meyer, JM ;
Vassalli, P ;
Garcia, I .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (07) :1699-1703
[5]   Estradiol repression of tumor necrosis factor-α transcription requires estrogen receptor activation function-2 and is enhanced by coactivators [J].
An, JP ;
Ribeiro, RCJ ;
Webb, P ;
Gustafsson, JÅ ;
Kushner, PJ ;
Baxter, JD ;
Leitman, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :15161-15166
[6]   A subset of nuclear receptor coregulators act as coupling proteins during synthesis and maturation of RNA transcripts [J].
Auboeuf, D ;
Dowhan, DH ;
Dutertre, M ;
Martin, N ;
Berget, SM ;
O'Malley, BW .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (13) :5307-5316
[7]   IMMUNOSUPPRESSION BY GLUCOCORTICOIDS - INHIBITION OF NF-KAPPA-B ACTIVITY THROUGH INDUCTION OF I-KAPPA-B SYNTHESIS [J].
AUPHAN, N ;
DIDONATO, JA ;
ROSETTE, C ;
HELMBERG, A ;
KARIN, M .
SCIENCE, 1995, 270 (5234) :286-290
[8]   Nuclear receptor coregulators: their modification codes and regulatory mechanism by translocation [J].
Baek, SH ;
Rosenfeld, MG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 319 (03) :707-714
[9]   Corticosteroids: The drugs to beat [J].
Barnes, PJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 533 (1-3) :2-14
[10]   Allergy review series VII: Intracellular signaling and regulation of allergic reactions - Molecular mechanisms of corticosteroids in allergic diseases [J].
Barnes, PJ .
ALLERGY, 2001, 56 (10) :928-936