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糖皮质激素受体信号传导的新见解——不仅仅是一种配体结合受体

New Insights in Glucocorticoid Receptor Signaling-More Than Just a Ligand-Binding Receptor.

作者信息

Scheschowitsch Karin, Leite Jacqueline Alves, Assreuy Jamil

机构信息

Department of Pharmacology, Universidade Federal de Santa Catarina , Florianópolis , Brazil.

Department of Pharmacology, Institute of Biomedical Sciences, Universidade de São Paulo , São Paulo , Brazil.

出版信息

Front Endocrinol (Lausanne). 2017 Feb 6;8:16. doi: 10.3389/fendo.2017.00016. eCollection 2017.

Abstract

The clinical use of classical glucocorticoids (GC) is narrowed by the many side effects it causes and the resistance to GC observed in some diseases. Since the great majority of GC effects depend on the activation of a glucocorticoid receptor (GR), many research groups had focused to better understand the signaling pathways involving those receptors. Transgenic animal models and genetic modifications of the receptor brought a huge insight into GR mechanisms of action. This in turn opened a new window for the search of selective GR modulators that ideally may have agonistic and antagonistic combined effects and activate one specific signaling pathway, inducing mostly transrepression or transactivation mechanisms. Another important research field concerns to posttranslational modifications that affect the GR and consequently also affect its signaling and function. In this mini review, we discuss many of those aspects of GR signaling, as well as findings like the ligand-independent activation of GR, which add another layer of complexity in GR signaling pathways. Although several recent data have been added to the GR field, much work has yet to be done, especially to find out the biological relevance of those alternative GR signaling pathways. Improving the knowledge about alternative GR signaling pathways and understanding how these pathways intercommunicate and in which situations they are relevant might help to develop new strategies to take benefit of it and to improve GC or other compounds efficacy causing minimal side effects.

摘要

传统糖皮质激素(GC)的临床应用因所引发的诸多副作用以及在某些疾病中观察到的对GC的耐药性而受到限制。由于绝大多数GC效应依赖于糖皮质激素受体(GR)的激活,许多研究团队致力于更深入地了解涉及这些受体的信号通路。转基因动物模型以及受体的基因改造为GR的作用机制带来了巨大的启示。这反过来又为寻找选择性GR调节剂打开了一扇新窗口,理想情况下,这些调节剂可能具有激动和拮抗的联合效应,并激活一条特定的信号通路,主要诱导转抑制或转激活机制。另一个重要的研究领域涉及影响GR的翻译后修饰,进而也影响其信号传导和功能。在这篇小型综述中,我们讨论了GR信号传导的诸多方面,以及诸如GR的非配体依赖性激活等发现,这些发现为GR信号通路增添了另一层复杂性。尽管最近在GR领域增加了一些数据,但仍有许多工作要做,特别是要弄清楚这些替代性GR信号通路的生物学相关性。增进对替代性GR信号通路的了解,理解这些通路如何相互沟通以及在哪些情况下它们相关,可能有助于制定新策略以利用这些通路,并提高GC或其他化合物的疗效,同时使副作用最小化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8e1/5292432/407ba949ed1b/fendo-08-00016-g001.jpg

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