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Influence of Transporter Polymorphisms on Drug Disposition and Response: A Perspective from the International Transporter Consortium

机译:转运蛋白多态性对药物处置和响应的影响:国际转运蛋白联盟的视角

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摘要

Advances in genomic technologies have led to a wealth of information identifying genetic polymorphisms in membrane transporters, specifically how these polymorphisms affect drug disposition and response. This review describes the current perspective of the International Transporter Consortium (ITC) on clinically important polymorphisms in membrane transporters. ITC suggests that in addition to previously recommended polymorphisms in ABCG2 (BCRP) and SLCO1B1 (OATP1B1), polymorphisms in the emerging transporter, SLC22A1 (OCT1), be considered during drug development. Collectively, polymorphisms in these transporters are important determinants of interindividual differences in the levels, toxicities, and response to many drugs.
机译:基因组技术的进步已导致大量信息鉴定膜转运蛋白中的遗传多态性,特别是这些多态性如何影响药物的处置和反应。这篇综述描述了国际转运蛋白协会(ITC)对膜转运蛋白临床上重要的多态性的当前观点。 ITC建议,除先前推荐的ABCG2(BCRP)和SLCO1B1(OATP1B1)多态性外,在药物开发过程中还应考虑新兴转运蛋白SLC22A1(OCT1)的多态性。总的来说,这些转运蛋白的多态性是水平,毒性和对多种药物反应的个体差异的重要决定因素。

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