孕烷X受体
雄激素受体
核受体
受体
异型生物质的
生物
药理学
计算生物学
生物化学
基因
转录因子
酶
作者
Xiaojuan Chai,Su Zeng,Wen Xie
标识
DOI:10.1517/17425255.2013.754010
摘要
PXR and CAR are both xenobiotic and endobiotic receptors. A remarkably diverse set of chemicals can activate PXR and CAR. There is significant cross-talk among xenobiotic receptors. Future studies are needed to focus on the polymorphisms of the nuclear receptors and the complex regulatory networks among nuclear receptors. Considerations should be given while designing PXR- or CAR-targeting pharmaceutics to avoid adverse drug effects. In the meantime, due to the diverse functions of PXR and CAR, agonists or antagonists for these receptors may have therapeutic potentials in managing certain diseases and enhancing therapeutic indexes.
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