利用 iPSC 模型进行人类遗传疾病的药物筛选。
Drug screening for human genetic diseases using iPSC models.
机构信息
Department of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
出版信息
Hum Mol Genet. 2018 Aug 1;27(R2):R89-R98. doi: 10.1093/hmg/ddy186.
Induced pluripotent stem cells (iPSCs) enable the generation of previously unattainable, scalable quantities of disease-relevant tissues from patients suffering from essentially any genetic disorder. This cellular material has proven instrumental for drug screening efforts on these disorders, and has facilitated the identification of novel therapeutics for patients. Here we will review the foundational technologies that have enabled iPSCs, the power and limitations of iPSC-based compound screens along with screening guidelines, and recent examples of screening efforts. Additionally we will provide a brief commentary on the future scientific roadmap using pluripotent- and 3D organoid-based, combinatorial approaches.
诱导多能干细胞 (iPSCs) 可从患有各种遗传疾病的患者中生成以前无法获得的、可扩展的疾病相关组织。这些细胞材料对于这些疾病的药物筛选工作非常重要,并为患者确定了新的治疗方法。在这里,我们将回顾使 iPSCs 成为可能的基础技术,基于 iPSC 的化合物筛选的优势和局限性以及筛选指南,以及最近的筛选工作示例。此外,我们将简要讨论使用多能干细胞和 3D 类器官的组合方法的未来科学路线图。