Three-Dimensional in Vitro Cell Culture Models in Drug Discovery and Drug Repositioning

药物发现 药品 药物开发 高通量筛选 计算生物学 鉴定(生物学) 体内 药物重新定位 细胞培养 药理学 计算机科学 医学 生物信息学 生物 生物技术 遗传学 植物
作者
Sigrid A. Langhans
出处
期刊:Frontiers in Pharmacology [Frontiers Media]
卷期号:9 被引量:1287
标识
DOI:10.3389/fphar.2018.00006
摘要

Drug development is a lengthy and costly process that proceeds through several stages from target identification to lead discovery and optimization, preclinical validation and clinical trials culminating in approval for clinical use. An important step in this process is high-throughput screening (HTS) of small compound libraries for lead identification. Currently, the majority of cell-based HTS is being carried out on cultured cells propagated in two-dimensions (2D) on plastic surfaces optimized for tissue culture. At the same time, compelling evidence suggests that cells cultured in these non-physiological conditions are not representative of cells residing in the complex microenvironment of a tissue. This discrepancy is thought to be a significant contributor to the high failure rate in drug discovery, where only a low percentage of drugs investigated ever make it through the gamut of testing and approval to the market. Thus, three-dimensional (3D) cell culture technologies that more closely resemble in vivo cell environments are now being pursued with intensity as they are expected to accommodate better precision in drug discovery. Here we will review common approaches to 3D culture, discuss the significance of 3D cultures in drug resistance and drug repositioning and address some of the challenges of applying 3D cell cultures to high-throughput drug discovery.
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