期刊
EXPERT OPINION ON DRUG DISCOVERY
卷 14, 期 4, 页码 343-353出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/17460441.2019.1577815
关键词
Zebrafish; phenotype; screening; cardiovascular
资金
- Starting Research Fund from the Shanghai Jiao Tong University
- European Union [794365]
- NIH (the National Heart, Lung, and Blood Institute)
- NIH (National Institute of Neurological Disorders and Stroke)
- NIH (Office of the Director)
- Burroughs Welcome Fund
- American Heart Association
- AstraZeneca
- Verily Life Sciences
- Marie Curie Actions (MSCA) [794365] Funding Source: Marie Curie Actions (MSCA)
Introduction: Our understanding of the complexity of cardiovascular disease pathophysiology remains very incomplete and has hampered cardiovascular drug development over recent decades. The prevalence of cardiovascular diseases and their increasing global burden call for novel strategies to address disease biology and drug discovery. Areas covered: This review describes the recent history of cardiovascular drug discovery using in vivo phenotype-based screening in zebrafish. The rationale for the use of this model is highlighted and the initial efforts in the fields of disease modeling and high-throughput screening are illustrated. Finally, the advantages and limitations of in vivo zebrafish screening are discussed, highlighting newer approaches, such as genome editing technologies, to accelerate our understanding of disease biology and the development of precise disease models. Expert opinion: Full understanding and faithful modeling of specific cardiovascular disease is a rate-limiting step for cardiovascular drug discovery. The resurgence of in vivo phenotype screening together with the advancement of systems biology approaches allows for the identification of lead compounds which show efficacy on integrative disease biology in the absence of validated targets. This strategy bypasses current gaps in knowledge of disease biology and paves the way for successful drug discovery and downstream molecular target identification.
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