Drug Repositioning by Kernel-Based Integration of Molecular Structure, Molecular Activity, and Phenotype Data
文献类型：期刊论文
| 作者 | Wang, Yongcui ; Chen, Shilong ; Deng, Naiyang ; Wang, Yong ; Wang, Y (reprint author), Chinese Acad Sci, Acad Math & Syst Sci, Natl Ctr Math & Interdisciplinary Sci, Beijing, Peoples R China. |
| 刊名 | PLOS ONE
 ; Wang, YC; Chen, SL; Deng, NY; Wang, Y.Drug Repositioning by Kernel-Based Integration of Molecular Structure, Molecular Activity, and Phenotype Data,PLOS ONE,2013,8(11):
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| 出版日期 | 2013-11-11 |
| 英文摘要 | Computational inference of novel therapeutic values for existing drugs, i.e., drug repositioning, offers the great prospect for faster and low-risk drug development. Previous researches have indicated that chemical structures, target proteins, and side-effects could provide rich information in drug similarity assessment and further disease similarity. However, each single data source is important in its own way and data integration holds the great promise to reposition drug more accurately. Here, we propose a new method for drug repositioning, PreDR (Predict Drug Repositioning), to integrate molecular structure, molecular activity, and phenotype data. Specifically, we characterize drug by profiling in chemical structure, target protein, and side-effects space, and define a kernel function to correlate drugs with diseases. Then we train a support vector machine (SVM) to computationally predict novel drug-disease interactions. PreDR is validated on a well-established drug-disease network with 1,933 interactions among 593 drugs and 313 diseases. By cross-validation, we find that chemical structure, drug target, and side-effects information are all predictive for drug-disease relationships. More experimentally observed drug-disease interactions can be revealed by integrating these three data sources. Comparison with existing methods demonstrates that PreDR is competitive both in accuracy and coverage. Follow-up database search and pathway analysis indicate that our new predictions are worthy of further experimental validation. Particularly several novel predictions are supported by clinical trials databases and this shows the significant prospects of PreDR in future drug treatment. In conclusion, our new method, PreDR, can serve as a useful tool in drug discovery to efficiently identify novel drug-disease interactions. In addition, our heterogeneous data integration framework can be applied to other problems.; Computational inference of novel therapeutic values for existing drugs, i.e., drug repositioning, offers the great prospect for faster and low-risk drug development. Previous researches have indicated that chemical structures, target proteins, and side-effects could provide rich information in drug similarity assessment and further disease similarity. However, each single data source is important in its own way and data integration holds the great promise to reposition drug more accurately. Here, we propose a new method for drug repositioning, PreDR (Predict Drug Repositioning), to integrate molecular structure, molecular activity, and phenotype data. Specifically, we characterize drug by profiling in chemical structure, target protein, and side-effects space, and define a kernel function to correlate drugs with diseases. Then we train a support vector machine (SVM) to computationally predict novel drug-disease interactions. PreDR is validated on a well-established drug-disease network with 1,933 interactions among 593 drugs and 313 diseases. By cross-validation, we find that chemical structure, drug target, and side-effects information are all predictive for drug-disease relationships. More experimentally observed drug-disease interactions can be revealed by integrating these three data sources. Comparison with existing methods demonstrates that PreDR is competitive both in accuracy and coverage. Follow-up database search and pathway analysis indicate that our new predictions are worthy of further experimental validation. Particularly several novel predictions are supported by clinical trials databases and this shows the significant prospects of PreDR in future drug treatment. In conclusion, our new method, PreDR, can serve as a useful tool in drug discovery to efficiently identify novel drug-disease interactions. In addition, our heterogeneous data integration framework can be applied to other problems. |
| 源URL | [http://ir.nwipb.ac.cn/handle/363003/3900]  |
| 专题 | 西北高原生物研究所_中国科学院西北高原生物研究所 |
| 推荐引用方式 GB/T 7714 | Wang, Yongcui,Chen, Shilong,Deng, Naiyang,et al. Drug Repositioning by Kernel-Based Integration of Molecular Structure, Molecular Activity, and Phenotype Data[J]. PLOS ONE, Wang, YC; Chen, SL; Deng, NY; Wang, Y.Drug Repositioning by Kernel-Based Integration of Molecular Structure, Molecular Activity, and Phenotype Data,PLOS ONE,2013,8(11):,2013. |
| APA | Wang, Yongcui,Chen, Shilong,Deng, Naiyang,Wang, Yong,&Wang, Y .(2013).Drug Repositioning by Kernel-Based Integration of Molecular Structure, Molecular Activity, and Phenotype Data.PLOS ONE. |
| MLA | Wang, Yongcui,et al."Drug Repositioning by Kernel-Based Integration of Molecular Structure, Molecular Activity, and Phenotype Data".PLOS ONE (2013). |
入库方式： OAI收割
来源：西北高原生物研究所
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