Systematic Drug Repositioning for a Wide Range of Diseases with Integrative Analyses of Phenotypic and Molecular Data

被引:56
作者
Iwata, Hiroaki [1 ]
Sawada, Ryusuke [1 ]
Mizutani, Sayaka [2 ]
Yamanishi, Yoshihiro [1 ,3 ]
机构
[1] Kyushu Univ, Med Inst Bioregulat, Multiscale Res Ctr Med Sci, Div Syst Cohort,Higashi Ku, Fukuoka, Fukuoka 8128582, Japan
[2] Kyoto Univ, Inst Chem Res, Bioinformat Ctr, Kyoto 6110011, Japan
[3] Kyushu Univ, Inst Adv Study, Higashi Ku, Fukuoka, Fukuoka 8128582, Japan
关键词
INTERFERON-ALPHA; IN-VITRO; PREDNISONE; EXPRESSION; THERAPY; GEMCITABINE; DISCOVERY; ARTHRITIS; NETWORKS; PATIENT;
D O I
10.1021/ci500670q
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Drug repositioning, or the appslication of known drugs to new indications, is a challenging issue in pharmaceutical science. In this study, we developed a new computational method to predict unknown drug indications for systematic drug repositioning in a framework of supervised network inference. We defined a descriptor for each drug-disease pair based on the phenotypic features of drugs (e.g., medicinal effects and side effects) and various molecular features of diseases (e.g., disease-causing genes, diagnostic markers, disease-related pathways, and environmental factors) and constructed a statistical model to predict new drug-disease associations for a wide range of diseases in the International Classification of Diseases. Our results show that the proposed method outperforms previous methods in terms of accuracy and applicability, and its performance does not depend on drug chemical structure similarity. Finally, we performed a comprehensive prediction of a drug-disease association network consisting of 2349 drugs and 858 diseases and described biologically meaningful examples of newly predicted drug indications for several types of cancers and nonhereditary diseases.
引用
收藏
页码:446 / 459
页数:14
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