Lai Yurong, Hsiao Peng
Pharmaceutical Candidate Optimization, Bristol-Myers Squibb, Princeton, NJ 08543.
Curr Pharm Des. 2014;20(10):1577-94. doi: 10.2174/13816128113199990467.
Over the recent years there has been a greater appreciation in the important roles drug transporters play in drug-drug interactions (DDI), safety and effectiveness of drugs. Notable consequence of this recognition includes the white paper published by the International Transporter Consortium (ITC) and the guidance documents drafted by regulatory agencies for investigating transporter-mediated DDIs during drug development. While DDIs as a result of transporter-mediated alterations in drug absorption, disposition, or excretion are typically undesirable, there are exceptions. When specific transporters selectively regulate the exposure of a drug at the site of action and/or toxicity, the use of these transporters as molecular targets has been proposed as a promising strategy for tissue-selective drug delivery to enhance efficacy or mitigate toxicity. Furthermore, membrane transporters play a pivotal role in the transport of nutrients and endogenous compounds into or out of cells to sustain cell survival. Genetic polymorphism of drug transporters as well as transporter-inhibiting drugs can alter the transporter functional activity and/or protein expression, causing transporter-specific diseases. Therefore, investigating drug-transporter interactions is a critical aspect in candidate drug selection, in order to enhance the pharmacological effects and/or prevent the unintended off-target toxicity. The goal of this review is to provide the drug discovery scientists with a cadre of concepts beyond the ITC White Paper that facilitate rational drug design for optimal safety and efficacy. To that end, this review focuses on the following aspects: 1) regulatory landscape on drug transporter-mediated DDIs, 2) transporter related organ toxicity, 3) utility of drug transporters for target organ delivery, and 4) to highlight the diseases known thus far that are associated with variants of transporter genes.
近年来,人们越来越认识到药物转运体在药物相互作用(DDI)、药物安全性和有效性方面所起的重要作用。这一认识的显著成果包括国际转运体联盟(ITC)发表的白皮书以及监管机构起草的关于在药物开发过程中研究转运体介导的药物相互作用的指导文件。虽然由转运体介导的药物吸收、处置或排泄改变导致的药物相互作用通常是不良的,但也有例外情况。当特定转运体选择性地调节药物在作用部位和/或毒性部位的暴露时,将这些转运体用作分子靶点已被提议作为一种有前景的策略,用于组织选择性药物递送以提高疗效或减轻毒性。此外,膜转运体在营养物质和内源性化合物进出细胞的转运中起着关键作用,以维持细胞存活。药物转运体的基因多态性以及转运体抑制药物可改变转运体的功能活性和/或蛋白质表达,导致特定转运体相关疾病。因此,研究药物 - 转运体相互作用是候选药物选择中的一个关键方面,以增强药理作用和/或预防意外的脱靶毒性。本综述的目的是为药物发现科学家提供一系列超越ITC白皮书的概念,以促进合理的药物设计,实现最佳的安全性和有效性。为此,本综述重点关注以下几个方面:1)药物转运体介导的药物相互作用的监管格局,2)与转运体相关的器官毒性,3)药物转运体在靶器官递送中的应用,4)突出迄今已知的与转运体基因变异相关的疾病。