Estrada Karol
Translational Genome Sciences, Biogen, Cambridge, MA, USA.
Methods Mol Biol. 2018;1793:277-290. doi: 10.1007/978-1-4939-7868-7_16.
The most important promise of the human genome sequencing project is the identification of the genetic cause of devastating human diseases and the subsequent deliver of novel drug therapies to treat these diseases with high unmet medical need. In the last 10 years we have successfully identified hundreds of genetic loci associated with many traits and diseases. The translation of these findings into novel therapies is not straightforward and poses challenges that are usually overlooked in traditional gene mapping. This chapter describes some of the most common challenges and opportunities to use human genetics to identify and validate novel drug targets.
人类基因组测序计划最重要的前景是确定毁灭性人类疾病的遗传病因,并随后提供新型药物疗法来治疗这些存在高度未满足医疗需求的疾病。在过去十年中,我们已成功确定了数百个与许多性状和疾病相关的基因座。将这些研究结果转化为新型疗法并非易事,并且带来了一些在传统基因定位中通常被忽视的挑战。本章描述了利用人类遗传学来识别和验证新型药物靶点的一些最常见挑战与机遇。