Drug repositioning by integrating target information through a heterogeneous network model

被引:255
|
作者
Wang, Wenhui [1 ,2 ]
Yang, Sen [1 ]
Zhang, Xiang [1 ]
Li, Jing [1 ]
机构
[1] Case Western Reserve Univ, Dept Elect Engn & Comp Sci, Cleveland, OH 44106 USA
[2] Univ So Calif, Los Angeles, CA 90089 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
CELL LUNG-CANCER; HUNTINGTONS-DISEASE; GENES; IDENTIFICATION; PREDICTION;
D O I
10.1093/bioinformatics/btu403
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: The emergence of network medicine not only offers more opportunities for better and more complete understanding of the molecular complexities of diseases, but also serves as a promising tool for identifying new drug targets and establishing new relationships among diseases that enable drug repositioning. Computational approaches for drug repositioning by integrating information from multiple sources and multiple levels have the potential to provide great insights to the complex relationships among drugs, targets, disease genes and diseases at a system level. Results: In this article, we have proposed a computational framework based on a heterogeneous network model and applied the approach on drug repositioning by using existing omics data about diseases, drugs and drug targets. The novelty of the framework lies in the fact that the strength between a disease-drug pair is calculated through an iterative algorithm on the heterogeneous graph that also incorporates drug-target information. Comprehensive experimental results show that the proposed approach significantly outperforms several recent approaches. Case studies further illustrate its practical usefulness.
引用
收藏
页码:2923 / 2930
页数:8
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