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细胞色素 P450 相关受体和孕烷 X 受体在异源生物感知和代谢中的作用。

Role of CAR and PXR in xenobiotic sensing and metabolism.

机构信息

St. Jude Children's Research Hospital, Department of Chemical Biology and Therapeutics, 262 Danny Thomas Place, Memphis, TN 38105, USA.

出版信息

Expert Opin Drug Metab Toxicol. 2012 Jul;8(7):803-17. doi: 10.1517/17425255.2012.685237. Epub 2012 May 3.

DOI:10.1517/17425255.2012.685237
PMID:22554043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3593589/
Abstract

INTRODUCTION

The xenobiotic detoxification system, which protects the human body from external chemicals, comprises drug-metabolizing enzymes and transporters whose expressions are regulated by pregnane X receptor (PXR) and the constitutive androstane receptor (CAR). The progress made in a large number of recent studies calls for a timely review to summarize and highlight these key discoveries.

AREAS COVERED

This review summarizes recent advances in elucidating the roles of PXR and CAR in the xenobiotic detoxification system. It also highlights the progress in understanding the regulation of PXR and CAR activity at the post-translational levels, as well as the structural basis for the regulation of these two xenobiotic sensors.

EXPERT OPINION

Future efforts are needed to discover novel agonists and antagonists with species and isoform selectivity, to systematically understand the regulation of PXR and CAR at multiple levels (transcriptional, post-transcriptional and post-translational levels) in response to xenobiotics exposure, and to solve the structures of the full-length receptors, which will be enabled by improved protein expression and purification techniques and approaches. In addition, more efforts will be needed to validate PXR and CAR as disease-related therapeutic targets and thus expand their roles as master xenobiotic sensors.

摘要

简介

人体的外来化合物解毒系统可保护机体免受外源性化学物质的侵害,其组成包括药物代谢酶和转运体,其表达受孕烷 X 受体 (PXR) 和组成型雄烷受体 (CAR) 调控。 大量近期研究的进展需要及时进行综述,以总结和强调这些关键发现。

涵盖领域

本综述总结了近年来阐明 PXR 和 CAR 在外来化合物解毒系统中的作用的最新进展。 它还强调了在理解 PXR 和 CAR 活性的翻译后水平调节以及这两种外来传感器调节的结构基础方面取得的进展。

专家意见

需要进一步努力发现具有物种和同工型选择性的新型激动剂和拮抗剂,系统地了解外源性物质暴露时 PXR 和 CAR 在多个水平(转录、转录后和翻译后水平)的调节,并解决全长受体的结构问题,这将得益于改进的蛋白质表达和纯化技术和方法。 此外,还需要进一步努力将 PXR 和 CAR 验证为与疾病相关的治疗靶点,从而扩大它们作为主要外来化合物传感器的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d6b/3593589/e7a3a01021d0/nihms-449963-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d6b/3593589/3dca66562fcf/nihms-449963-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d6b/3593589/dca8a4c2e69c/nihms-449963-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d6b/3593589/e7a3a01021d0/nihms-449963-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d6b/3593589/3dca66562fcf/nihms-449963-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d6b/3593589/dca8a4c2e69c/nihms-449963-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d6b/3593589/e7a3a01021d0/nihms-449963-f0003.jpg

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