Integrated Approaches to Drug Discovery for Oxidative Stress-Related Retinal Diseases

被引:9
|
作者
Nishimura, Yuhei [1 ]
Hara, Hideaki [2 ]
机构
[1] Mie Univ, Dept Mol & Cellular Pharmacol, Pharmacogen & Pharmacoinformat, Grad Sch Med, Tsu, Mie 5148507, Japan
[2] Gifu Pharmaceut Univ, Dept Biofunct Evaluat, Mol Pharmacol, Gifu 5011196, Japan
基金
日本学术振兴会;
关键词
RENIN-ANGIOTENSIN SYSTEM; GENOME-WIDE ASSOCIATION; MACULAR DEGENERATION; SUSCEPTIBILITY LOCI; NEURAL RETINA; MOUSE MODEL; CELL-DEATH; RECEPTOR; ZEBRAFISH; PROTEIN;
D O I
10.1155/2016/2370252
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Excessive oxidative stress induces dysregulation of functional networks in the retina, resulting in retinal diseases such as glaucoma, age-related macular degeneration, and diabetic retinopathy. Although various therapies have been developed to reduce oxidative stress in retinal diseases, most have failed to show efficacy in clinical trials. This may be due to oversimplification of target selection for such a complex network as oxidative stress. Recent advances in high-throughput technologies have facilitated the collection of multilevel omics data, which has driven growth in public databases and in the development of bioinformatics tools. Integration of the knowledge gained from omics databases can be used to generate disease-related biological networks and to identify potential therapeutic targets within the networks. Here, we provide an overview of integrative approaches in the drug discovery process and provide simple examples of how the approaches can be exploited to identify oxidative stress-related targets for retinal diseases.
引用
收藏
页数:9
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