转换抑制
交易激励
糖皮质激素受体
糖皮质激素
药品
治疗指标
药理学
哮喘
药物开发
医学
不利影响
CYP3A4型
生物信息学
计算生物学
化学
免疫学
生物
转录因子
基因
内科学
生物化学
细胞色素P450
新陈代谢
作者
Mario Cazzola,Angelo Coppola,Paola Rogliani,Maria Gabriella Matera
标识
DOI:10.1517/13543784.2015.1078310
摘要
Introduction: Inhaled corticosteroids are the only drugs that effectively suppress the airway inflammation, but they can induce considerable systemic and adverse effects when they are administered chronically at high doses. Consequently, the pharmaceutical industry is still searching for newer entities with an improved therapeutic index.Areas covered: Herein, the authors review the research in the glucocorticoid field to identify ligands of the glucocorticoid receptor (GR). These ligands preferentially induce transrepression with little or no transactivating activity, in order to have a potent anti-inflammatory action and a low side-effects profile.Expert opinion: Several agents have been synthesized, but few have been tested in experimental models of asthma. Furthermore, only three (BI-54903, GW870086X and AZD5423) have entered clinical development, although the development of at least one of them (BI-54903) was discontinued. The reason for the limited success so far obtained is that the model of transactivation versus transrepression is a too simplistic representation of GR activity. It is difficult to uncouple the therapeutic and harmful effects mediated by GR, but some useful information that might change the current perspective is appearing in the literature. The generation of gene expression ‘fingerprints’ produced by different GR agonists in target and off-target human tissues could be useful in identifying drug candidates with an improved therapeutic ratio.
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