糖皮质激素受体
糖皮质激素
信号转导
受体
细胞生物学
计算生物学
生物
遗传学
内分泌学
作者
Dorien Clarisse,Laura Van Moortel,Chloé Van Leene,Kris Gevaert,Karolien De Bosscher
标识
DOI:10.1016/j.tibs.2024.01.012
摘要
The glucocorticoid receptor (GR) is a major nuclear receptor (NR) drug target for the treatment of inflammatory disorders and several cancers. Despite the effectiveness of GR ligands, their systemic action triggers a plethora of side effects, limiting long-term use. Here, we discuss new concepts of and insights into GR mechanisms of action to assist in the identification of routes toward enhanced therapeutic benefits. We zoom in on the communication between different GR domains and how this is influenced by different ligands. We detail findings on the interaction between GR and chromatin, and highlight how condensate formation and coregulator confinement can perturb GR transcriptional responses. Last, we discuss the potential of novel ligands and the therapeutic exploitation of crosstalk with other NRs.
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