药物发现
诱导多能干细胞
多学科方法
药物开发
转化研究
疾病
计算生物学
医学
基因组编辑
计算机科学
生物信息学
数据科学
药品
药理学
生物
病理
基因
清脆的
社会学
胚胎干细胞
生物化学
社会科学
作者
Péter Horváth,Nathalie Aulner,Marc Bickle,Anthony M. Davies,Elaine Del Nery,Daniel Ebner,Marı́a C. Montoya,Päivi Östling,Vilja Pietiäinen,Leo Price,Spencer Shorte,Gerardo Turcatti,Carina von Schantz,Neil O. Carragher
摘要
The common and persistent failures to translate promising preclinical drug candidates into clinical success highlight the limited effectiveness of disease models currently used in drug discovery. An apparent reluctance to explore and adopt alternative cell- and tissue-based model systems, coupled with a detachment from clinical practice during assay validation, contributes to ineffective translational research. To help address these issues and stimulate debate, here we propose a set of principles to facilitate the definition and development of disease-relevant assays, and we discuss new opportunities for exploiting the latest advances in cell-based assay technologies in drug discovery, including induced pluripotent stem cells, three-dimensional (3D) co-culture and organ-on-a-chip systems, complemented by advances in single-cell imaging and gene editing technologies. Funding to support precompetitive, multidisciplinary collaborations to develop novel preclinical models and cell-based screening technologies could have a key role in improving their clinical relevance, and ultimately increase clinical success rates.
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