Department of Pharmaceutical Sciences, University at Buffalo, SUNY, Buffalo, NY 14260, USA.
Biopharm Drug Dispos. 2011 Sep;32(6):355-67. doi: 10.1002/bdd.764. Epub 2011 Jul 28.
Several noncoding microRNAs (miR or miRNA) have been shown to regulate the expression of drug-metabolizing enzymes and transporters. Xenobiotic drug-induced changes in enzyme and transporter expression may be associated with the alteration of miRNA expression. Therefore, this study investigated the impact of 19 xenobiotic drugs (e.g. dexamethasone, vinblastine, bilobalide and cocaine) on the expression of ten miRNAs (miR-18a, -27a, -27b, -124a, -148a, -324-3p, -328, -451, -519c and -1291) in MCF-7, Caco-2, SH-SY5Y and BE(2)-M17 cell systems. The data revealed that miRNAs were differentially expressed in human cell lines and the change in miRNA expression was dependent on the drug, as well as the type of cells investigated. Notably, treatment with bilobalide led to a 10-fold increase of miR-27a and a 2-fold decrease of miR-148a in Caco-2 cells, but no change of miR-27a and a 2-fold increase of miR-148a in MCF-7 cells. Neuronal miR-124a was generally down-regulated by psychoactive drugs (e.g. cocaine, methadone and fluoxetine) in BE(2)-M17 and SH-SY5Y cells. Dexamethasone and vinblastine, inducers of drug-metabolizing enzymes and transporters, suppressed the expression of miR-27b, -148a and -451 that down-regulate the enzymes and transporters. These findings should provide increased understanding of the altered gene expression underlying drug disposition, multidrug resistance, drug-drug interactions and neuroplasticity.
几种非编码 microRNA(miR 或 miRNA)已被证明可以调节药物代谢酶和转运体的表达。外源性药物诱导的酶和转运体表达的变化可能与 miRNA 表达的改变有关。因此,本研究调查了 19 种外源性药物(如地塞米松、长春碱、银杏内酯和可卡因)对 MCF-7、Caco-2、SH-SY5Y 和 BE(2)-M17 细胞系中 10 种 miRNA(miR-18a、-27a、-27b、-124a、-148a、-324-3p、-328、-451、-519c 和 -1291)表达的影响。数据显示,miRNA 在人细胞系中表达差异,miRNA 表达的变化取决于药物以及所研究的细胞类型。值得注意的是,银杏内酯处理导致 Caco-2 细胞中 miR-27a 增加 10 倍,miR-148a 减少 2 倍,但 MCF-7 细胞中 miR-27a 无变化,miR-148a 增加 2 倍。神经细胞 miR-124a 通常被精神活性药物(如可卡因、美沙酮和氟西汀)下调在 BE(2)-M17 和 SH-SY5Y 细胞中。地塞米松和长春碱是药物代谢酶和转运体的诱导剂,抑制了下调这些酶和转运体的 miR-27b、-148a 和 -451 的表达。这些发现应该增加对药物处置、多药耐药性、药物相互作用和神经可塑性的改变的基因表达的理解。