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Pharmacogenomics: Current State-of-the-Art

机译:药物基因组学:最新技术

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摘要

The completion of the human genome project 10 years ago was met with great optimism for improving drug therapy through personalized medicine approaches, with the anticipation that an era of genotype-guided patient prescribing was imminent. To some extent this has come to pass and a number of key pharmacogenomics markers of inter-individual drug response, for both safety and efficacy, have been identified and subsequently been adopted in clinical practice as pre-treatment genetic tests. However, the universal application of genetics in treatment guidance is still a long way off. This review will highlight important pharmacogenomic discoveries which have been facilitated by the human genome project and other milestone projects such as the International HapMap and 1000 genomes, and by the continued development of genotyping and sequencing technologies, including rapid point of care pre-treatment genetic testing. However, there are still many challenges to implementation for the many other reported biomarkers which continue to languish within the discovery phase. As technology advances over the next 10 years, and the costs fall, the field will see larger genetic data sets, including affordable whole genome sequences, which will, it is hoped, improve patient outcomes through better diagnostic, prognostic and predictive biomarkers.
机译:十年前人类基因组计划的完成使人们非常乐观,他们希望通过个性化的医学方法改善药物治疗,并期待着由基因型指导的患者处方时代的到来。在某种程度上,这已经成为现实,并且已经确定了多种个体间药物反应的重要药物基因组学标志物,以确保安全性和有效性,并随后在临床实践中用作治疗前的基因检测。但是,遗传学在治疗指导中的普遍应用还有很长的路要走。这篇综述将重点介绍重要的药物基因组学发现,人类基因组计划和其他里程碑计划(例如国际HapMap和1000个基因组)以及基因分型和测序技术的不断发展,包括快速的护理前预处理基因测试,都促进了这一发现。但是,对于许多其他报告的生物标记物,在实施过程中仍然存在许多挑战,这些发现在探索阶段仍将继续受到影响。随着未来10年技术的进步以及成本的下降,该领域将看到更大的遗传数据集,包括负担得起的全基因组序列,希望通过更好的诊断,预后和预测性生物标记物改善患者的治疗效果。

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