IRMB, University of Montpellier, INSERM, CHU Montpellier, 34295 Montpellier, France.
Cells. 2020 Oct 31;9(11):2395. doi: 10.3390/cells9112395.
Pregnane X receptor (PXR, NR1I2) and constitutive androstane receptor (CAR, NR1I3) are members of the nuclear receptor superfamily that mainly act as ligand-activated transcription factors. Their functions have long been associated with the regulation of drug metabolism and disposition, and it is now well established that they are implicated in physiological and pathological conditions. Considerable efforts have been made to understand the regulation of their activity by their cognate ligand; however, additional regulatory mechanisms, among which the regulation of their expression, modulate their pleiotropic effects. This review summarizes the current knowledge on and expression during development and adult life; tissue distribution; spatial, temporal, and metabolic regulations; as well as in pathological situations, including chronic diseases and cancers. The expression of CAR and PXR is modulated by complex regulatory mechanisms that involve the interplay of transcription factors and also post-transcriptional and epigenetic modifications. Moreover, many environmental stimuli affect CAR and PXR expression through mechanisms that have not been elucidated.
pregnane X 受体 (PXR,NR1I2) 和细胞色素 P450 诱导剂受体 (CAR,NR1I3) 是核受体超家族的成员,主要作为配体激活的转录因子发挥作用。它们的功能长期以来一直与药物代谢和处置的调节有关,现在已经确定它们与生理和病理状况有关。人们已经做出了相当大的努力来了解它们的同源配体对其活性的调节;然而,其他调节机制,包括它们的表达调节,调节它们的多效性作用。本综述总结了目前关于发育和成年期 和 表达、组织分布、时空和代谢调节以及慢性疾病和癌症等病理情况下的知识。CAR 和 PXR 的表达受复杂的调节机制的调节,这些机制涉及转录因子的相互作用以及转录后和表观遗传修饰。此外,许多环境刺激通过尚未阐明的机制影响 CAR 和 PXR 的表达。