Heterogeneity in mechanisms influencing glucocorticoid sensitivity: The need for a systems biology approach to treatment of glucocorticoid-resistant inflammation

被引:29
作者
Keenan, Christine R. [1 ]
Radojicic, Danica [1 ]
Li, Meina [1 ]
Radwan, Asmaa [1 ]
Stewart, Alastair G. [1 ]
机构
[1] Univ Melbourne, Dept Pharmacol & Therapeut, Lung Hlth Res Ctr, Parkville, Vic 3010, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Innate host defence; Cytokines; Airways; Asthma; COPD; Idiopathic pulmonary fibrosis; AIRWAY SMOOTH-MUSCLE; NF-KAPPA-B; 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-1; IDIOPATHIC PULMONARY-FIBROSIS; HISTONE DEACETYLASE ACTIVITY; BLOOD MONONUCLEAR-CELLS; RELATIVE CORTICOSTEROID INSENSITIVITY; FIBROBLAST-MEDIATED CONTRACTION; MESENCHYMAL STEM-CELLS; HUMAN LUNG FIBROBLASTS;
D O I
10.1016/j.pharmthera.2015.01.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glucocorticoids (GCs) have impressive anti-inflammatory and immunosuppressive effects.and show a diversity of actions across a variety of cell phenotypes. Implicit in efforts to optimize GCs as anti-inflammatory agents for any or all indications is the notion that the relevant mechanism(s) of action of GCs are fully elucidated. However, recent advances in understanding GC signalling mechanisms have revealed remarkable complexity and contextual dependence, calling into question whether the mechanisms of action are sufficiently well-described to embark on optimization. In the current review, we address evidence for differences in the mechanism of action in different cell types and contexts, and discuss contrasts in mechanisms of glucocorticoid insensitivity, with a focus on asthma and Chronic Obstructive Pulmonary Disease (COPD)..Given this complexity, we consider the potential breadth of impact and selectivity of strategies directed to reversing the glucocorticoid insensitivity. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:81 / 93
页数:13
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