Department of Biotechnology and Bioinformatics, Ranbaxy Research Laboratories, R&D III, Sec 18, Udyog Vihar, Gurgaon 122015, Haryana, India.
Drug Discov Today. 2011 Sep;16(17-18):793-9. doi: 10.1016/j.drudis.2011.08.003. Epub 2011 Aug 16.
The cytochrome P450 (CYP) enzymes, involved in the metabolism of therapeutic drugs, are the major determinants of drug half-life. From a drug industry perspective, variability in drug response owing to CYP polymorphisms makes CYP profiling a commercially interesting option for diagnosis, prognosis and predicting response to drug treatment. Recent studies highlighting microRNA-mediated regulation of CYP genes represents a major advance in our understanding of variations in individual drug responses. Herein we review new perspectives on the molecular mechanisms of CYP regulation and genotyping technologies. Together, these developments present novel therapeutic opportunities and help to explain the integrated response of cells to xenobiotic drug metabolism.
细胞色素 P450(CYP)酶参与治疗药物的代谢,是决定药物半衰期的主要因素。从制药行业的角度来看,由于 CYP 多态性导致的药物反应变异性使得 CYP 分析成为诊断、预后和预测药物治疗反应的商业上有趣的选择。最近的研究强调了 microRNA 对 CYP 基因的调节,这代表了我们对个体药物反应变化的理解的重大进展。本文综述了 CYP 调节和基因分型技术的分子机制的新观点。这些进展共同为新型治疗机会提供了依据,并有助于解释细胞对外源药物代谢的综合反应。