Cell and small animal models for phenotypic drug discovery

被引:35
作者
Szabo, Mihaly [1 ]
Akusjarvi, Sara Svensson [1 ]
Saxena, Ankur [1 ]
Liu, Jianping [2 ]
Chandrasekar, Gayathri [1 ]
Kitambi, Satish S. [1 ]
机构
[1] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Nobels Vag 16, S-17177 Solna, Sweden
[2] Karolinska Inst, Dept Biochem & Biophys, Solna, Sweden
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2017年 / 11卷
关键词
phenotype; screening; PDD; discovery; zebrafish; drug; IN-VIVO; CAENORHABDITIS-ELEGANS; HIGH-THROUGHPUT; DROSOPHILA-MELANOGASTER; DISEASE; PLATFORM; IMAGE; INFECTION; SYSTEMS; SCREEN;
D O I
10.2147/DDDT.S129447
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The phenotype-based drug discovery (PDD) approach is re-emerging as an alternative platform for drug discovery. This review provides an overview of the various model systems and technical advances in imaging and image analyses that strengthen the PDD platform. In PDD screens, compounds of therapeutic value are identified based on the phenotypic perturbations produced irrespective of target(s) or mechanism of action. In this article, examples of phenotypic changes that can be detected and quantified with relative ease in a cell-based setup are discussed. In addition, a higher order of PDD screening setup using small animal models is also explored. As PDD screens integrate physiology and multiple signaling mechanisms during the screening process, the identified hits have higher biomedical applicability. Taken together, this review highlights the advantages gained by adopting a PDD approach in drug discovery. Such a PDD platform can complement target-based systems that are currently in practice to accelerate drug discovery.
引用
收藏
页码:1957 / 1967
页数:11
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