Crosstalk between TNF and glucocorticoid receptor signaling pathways

被引:62
|
作者
Van Bogaert, Tom [1 ,2 ]
De Bosscher, Karolien [3 ]
Libert, Claude [1 ,2 ]
机构
[1] VIB, Dept Mol Biomed Res, Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, Ghent, Belgium
[3] Univ Ghent, Dept Physiol, LEGEST, Ghent, Belgium
关键词
TNF; Nuclear receptors; Crosstalk; Steroids; TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; CORTICOSTEROID-BINDING GLOBULIN; 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-1; EPITHELIAL SODIUM-CHANNEL; HISTONE H4 ACETYLATION; FACTOR-ALPHA; TRANSCRIPTIONAL ACTIVATION; C-JUN; DOWN-REGULATION;
D O I
10.1016/j.cytogfr.2010.04.003
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
TNF is a Janus-faced protein. It possesses impressive anti-tumor activities, but it is also one of the strongest known pro-inflammatory cytokines, which hampers its use as a systemic anti-cancer agent. TNF has been shown to play a detrimental role in inflammatory diseases such as rheumatoid arthritis and inflammatory bowel disease. Glucocorticoids are strongly anti-inflammatory and exert their therapeutic effects through binding to their receptor, the glucocorticoid receptor. Therefore, glucocorticoids have been used for over half a century for the treatment of inflammatory diseases. However, many patients are or become resistant to the therapeutic effects of glucocorticoids. Inflammatory cytokines have been suggested to play an important role in this steroid insensitivity or glucocorticoid resistance. This review aims to highlight the mechanisms of mutual inhibition between TNF and GR signaling pathways. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:275 / 286
页数:12
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