Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, 410008, People's Republic of China.
Cancer Chemother Pharmacol. 2014 Aug;74(2):217-27. doi: 10.1007/s00280-014-2494-9. Epub 2014 Jun 3.
Pregnane X receptor (PXR) is a member of the nuclear receptor superfamily that differently expresses not only in human normal tissues but also in numerous types of human cancers. PXR can be activated by many endogenous substances and exogenous chemicals, and thus affects chemotherapeutic effects and intervenes drug-drug interactions by regulating its target genes involving drug metabolism and transportation, cell proliferation and apoptosis, and modulating endobiotic homeostasis. Tissue and context-specific regulation of PXR contributes to diverse effects in the treatment for numerous cancers. Genetic variants of PXR lead to intra- and inter-individual differences in the expression and inducibility of PXR, resulting in different responses to chemotherapy in PXR-positive cancers. The purpose of this review is to summarize and discuss the role of PXR in the metabolism and clearance of anticancer drugs. It is also expected that this review will provide insights into PXR-mediated enhancement for chemotherapeutic treatment, prediction of drug-drug interactions and personalized medicine.
孕烷 X 受体 (PXR) 是核受体超家族的一员,不仅在人类正常组织中表达不同,而且在许多类型的人类癌症中也表达不同。PXR 可以被许多内源性物质和外源性化学物质激活,从而通过调节其涉及药物代谢和转运、细胞增殖和凋亡的靶基因,影响化学治疗效果并干预药物-药物相互作用,调节内源性物质的动态平衡。PXR 的组织和上下文特异性调节有助于治疗多种癌症产生不同的效果。PXR 的遗传变异导致 PXR 的表达和诱导性在个体内和个体间存在差异,从而导致 PXR 阳性癌症对化疗的反应不同。本综述的目的是总结和讨论 PXR 在抗癌药物代谢和清除中的作用。我们也希望本综述能为 PXR 介导的增强化疗治疗、预测药物-药物相互作用和个性化医学提供新的见解。