The molecular physiology of nuclear retinoic acid receptors. From health to disease

被引:106
作者
Duong, Vanessa [1 ]
Rochette-Egly, Cecile [1 ]
机构
[1] Univ Strasbourg, CNRS, INSERM, IGBMC,U596,UMR7104, F-67404 Illkirch Graffenstaden, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2011年 / 1812卷 / 08期
关键词
Nuclear retinoic acid receptors; Transcription; Homeostasis; Cancer; ACTIVATED PROTEIN-KINASE; UNION-OF-PHARMACOLOGY; RAR-ALPHA; X-RECEPTOR; SIGNALING PATHWAY; GENE-EXPRESSION; BREAST-CANCER; GRANULOCYTIC DIFFERENTIATION; RNA GRANULES; C/EBP-ALPHA;
D O I
10.1016/j.bbadis.2010.10.007
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 nuclear retinoic acid (RA) receptors (RAR alpha, beta and gamma) are transcriptional transregulators, which control the expression of specific gene subsets subsequently to ligand binding and to strictly controlled phosphorylation processes. Consequently RARs maintain homeostasis through the control of cell proliferation and differentiation. Today, it is admitted that, analogous to the paradigm established by the hematopoietic system, most adult tissues depict a differentiation hierarchy starting from rare stem cells. Here we highlight that the integrity of RARs is absolutely required for homeostasis in adults. Indeed, strictly controlled levels of RARs are necessary for the correct balance between self-renewal and differentiation of tissue stem cells. In addition, loss, accumulation, mutations or aberrant modifications of a specific RAR lead to uncontrolled proliferation and/or to differentiation block and thereby to cancer. This article is part of a Special Issue entitled: Translating nuclear receptors from health to disease. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1023 / 1031
页数:9
相关论文
共 139 条
[1]   Activation of Rac1 and the p38 mitogen-activated protein kinase pathway in response to all-trans-retinoic acid [J].
Alsayed, Y ;
Uddin, S ;
Mahmud, N ;
Lekmine, F ;
Kalvakolanu, DV ;
Minucci, S ;
Bokoch, G ;
Platanias, LC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (06) :4012-4019
[2]   The promise of retinoids to fight against cancer [J].
Altucci, L ;
Gronemeyer, H .
NATURE REVIEWS CANCER, 2001, 1 (03) :181-193
[3]   Synaptic Signaling by All-Trans Retinoic Acid in Homeostatic Synaptic Plasticity [J].
Aoto, Jason ;
Nam, Christine I. ;
Poon, Michael M. ;
Ting, Pamela ;
Chen, Lu .
NEURON, 2008, 60 (02) :308-320
[4]   TFIIH interacts with the retinoic acid receptor γ and phosphorylates its AF-1-activating domain through cdk7 [J].
Bastien, J ;
Adam-Stitah, S ;
Riedl, T ;
Egly, JM ;
Chambon, P ;
Rochette-Egly, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (29) :21896-21904
[5]   Crosstalk in Inflammation: The Interplay of Glucocorticoid Receptor-Based Mechanisms and Kinases and Phosphatases [J].
Beck, Ilse M. E. ;
Vanden Berghe, Wim ;
Vermeulen, Linda ;
Yamamoto, Keith R. ;
Haegeman, Guy ;
De Bosscher, Karolien .
ENDOCRINE REVIEWS, 2009, 30 (07) :830-882
[6]   Glucocorticoids and mitogen- and stress-activated protein kinase 1 inhibitors: Possible partners in the combat against inflammation [J].
Beck, Ilse M. E. ;
Vanden Berghe, Wim ;
Gerlo, Sarah ;
Bougarne, Nadia ;
Vermeulen, Linda ;
De Bosscher, Karolien ;
Haegeman, Guy .
BIOCHEMICAL PHARMACOLOGY, 2009, 77 (07) :1194-1205
[7]   All-trans-Retinoic Acid Represses Obesity and Insulin Resistance by Activating both Peroxisome Proliferation-Activated Receptor β/δ and Retinoic Acid Receptor [J].
Berry, Daniel C. ;
Noy, Noa .
MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (12) :3286-3296
[8]   Differentiation of mouse embryonic stem cells into a defined neuronal lineage [J].
Bibel, M ;
Richter, J ;
Schrenk, K ;
Tucker, KL ;
Staiger, V ;
Korte, M ;
Goetz, M ;
Barde, YA .
NATURE NEUROSCIENCE, 2004, 7 (09) :1003-1009
[9]   Oncogenic kinase signalling [J].
Blume-Jensen, P ;
Hunter, T .
NATURE, 2001, 411 (6835) :355-365
[10]  
Boudjelal M, 2000, CANCER RES, V60, P2247