Nakano Masataka, Nakajima Miki
WPI Nano Life Science Institute, Kanazawa University.
Drug Metabolism and Toxicology, Faculty of Pharmaceutical Sciences, Kanazawa University.
Nihon Yakurigaku Zasshi. 2019;154(1):28-34. doi: 10.1254/fpj.154.28.
Drug metabolism is an important determinant to control pharmacokinetics, drug response and drug toxicity. Large variabilities are observed in expression or activity of drug-metabolizing enzymes such as cytochrome P450 (CYP) and UDP-glucuronosyltransferase (UGT). Therefore, understanding of the causes for the variation of drug metabolism potencies is essential for efficient drug development and promotion of safe use of medicines. The expression of drug-metabolizing enzymes is controlled by transcriptional regulation by nuclear receptors and transcriptional factors, and by epigenetic regulation such as DNA methylation and histone acetylation. In addition to such regulatory mechanisms, recent studies revealed that microRNAs (miRNAs) significantly contribute to post-transcriptional regulation of drug-metabolizing enzymes. miRNAs are endogenous ~22-nucleotide non-coding RNAs that regulate gene expression through the translational repression and degradation of mRNAs. More recently, it has been clarified that the presence of pseudogenes or single nucleotide polymorphisms as well as RNA editing event affect miRNA-dependent regulation. It is unwavering fact that miRNAs significantly contribute to inter- and intra-individual differences in the expression of drug-metabolizing enzymes. In this review, we introduce current knowledge of miRNA-mediated regulation of drug metabolism.
药物代谢是控制药代动力学、药物反应和药物毒性的重要决定因素。在细胞色素P450(CYP)和尿苷二磷酸葡萄糖醛酸基转移酶(UGT)等药物代谢酶的表达或活性方面存在很大差异。因此,了解药物代谢能力差异的原因对于高效药物开发和促进药物安全使用至关重要。药物代谢酶的表达受核受体和转录因子的转录调控以及DNA甲基化和组蛋白乙酰化等表观遗传调控的控制。除了这些调控机制外,最近的研究表明,微小RNA(miRNA)对药物代谢酶的转录后调控有显著作用。miRNA是内源性的约22个核苷酸的非编码RNA,通过mRNA的翻译抑制和降解来调节基因表达。最近,已经明确假基因或单核苷酸多态性的存在以及RNA编辑事件会影响miRNA依赖性调控。miRNA对药物代谢酶表达的个体间和个体内差异有显著作用,这是毋庸置疑的事实。在本综述中,我们介绍了miRNA介导的药物代谢调控的当前知识。