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人诱导多能干细胞衍生的患者组织和 3D 细胞培养物第一部分:靶标鉴定和先导化合物优化。

Human iPS Cell-Derived Patient Tissues and 3D Cell Culture Part 1: Target Identification and Lead Optimization.

机构信息

1 Corning Life Sciences, Tewksbury, MA, USA.

2 Santa Cruz, CA, USA.

出版信息

SLAS Technol. 2019 Feb;24(1):3-17. doi: 10.1177/2472630318803277. Epub 2018 Oct 4.

Abstract

Human-induced pluripotent stem cells (HiPSCs), and new technologies to culture them into functional cell types and tissues, are now aiding drug discovery. Patient-derived HiPSCs can provide disease models that are more clinically relevant and so more predictive than the currently available animal-derived or tumor cell-derived cells. These cells, consequently, exhibit disease phenotypes close to the human pathology, particularly when cultured under conditions that allow them to recapitulate the tissue architecture in three-dimensional (3D) systems. A key feature of HiPSCs is that they can be cultured under conditions that favor formation of multicellular spheroids or organoids. By culturing and differentiating in systems mimicking the human tissue in vivo, the HiPSC microenvironment further reflects patient in vivo physiology, pathophysiology, and ultimately pharmacological responsiveness. We assess the rationale for using HiPSCs in several phases of preclinical drug discovery, specifically in disease modeling, target identification, and lead optimization. We also discuss the growing use of HiPSCs in compound lead optimization, particularly in profiling compounds for their potential metabolic liability and off-target toxicities. Collectively, we contend that both approaches, HiPSCs and 3D cell culture, when used in concert, have exciting potential for the development of novel medicines.

摘要

人诱导多能干细胞(HiPSCs)和培养它们成为功能性细胞类型和组织的新技术,现在正在辅助药物发现。源自患者的 HiPSCs 可以提供更具临床相关性和预测性的疾病模型,比目前可用的动物源性或肿瘤细胞源性细胞更具预测性。这些细胞因此表现出更接近人类病理学的疾病表型,特别是在允许它们在三维(3D)系统中再现组织架构的条件下进行培养时。HiPSCs 的一个关键特征是它们可以在有利于形成多细胞球体或类器官的条件下进行培养。通过在模拟体内人类组织的系统中进行培养和分化,HiPSC 微环境进一步反映了患者体内的生理学、病理生理学,最终是药物反应性。我们评估了在临床前药物发现的几个阶段使用 HiPSCs 的基本原理,特别是在疾病建模、靶点识别和先导化合物优化方面。我们还讨论了在化合物先导化合物优化中越来越多地使用 HiPSCs 的情况,特别是在评估化合物的潜在代谢毒性和非靶标毒性方面。总的来说,我们认为这两种方法,HiPSCs 和 3D 细胞培养,当协同使用时,对于开发新型药物具有令人兴奋的潜力。

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