Drug-target interaction prediction: databases, web servers and computational models

被引:507
作者
Chen, Xing [1 ]
Yan, Chenggang Clarence [2 ]
Zhang, Xiaotian [3 ]
Zhang, Xu [3 ]
Dai, Feng [4 ]
Yin, Jian [5 ]
Zhang, Yongdong [4 ]
机构
[1] Chinese Acad Sci, Natl Ctr Math & Interdisciplinary Sci, Zhongguancun East Rd, Beijing 100190, Peoples R China
[2] Tsinghua Univ, Dept Automat, Beijing, Peoples R China
[3] Shandong Univ, Sch Mech Elect & Informat Engn, Jinan, Peoples R China
[4] Chinese Acad Sci, Inst Comp Technol, Beijing, Peoples R China
[5] Shandong Univ, Dept Comp, Jinan, Peoples R China
关键词
drug-target interactions prediction; drug discovery; computational models; biological networks; machine learning; DIVERSITY-ORIENTED SYNTHESIS; CANCER SYSTEMS BIOLOGY; EXPRESSION PROFILES; DISCOVERY; NETWORK; RESOURCE; GENOME; INFORMATION; IDENTIFICATION; PHARMACOLOGY;
D O I
10.1093/bib/bbv066
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Identification of drug-target interactions is an important process in drug discovery. Although high-throughput screening and other biological assays are becoming available, experimental methods for drug-target interaction identification remain to be extremely costly, time-consuming and challenging even nowadays. Therefore, various computational models have been developed to predict potential drug-target associations on a large scale. In this review, databases and web servers involved in drug-target identification and drug discovery are summarized. In addition, we mainly introduced some state-of-the-art computational models for drug-target interactions prediction, including network-based method, machine learning-based method and so on. Specially, for the machine learning-based method, much attention was paid to supervised and semi-supervised models, which have essential difference in the adoption of negative samples. Although significant improvements for drug-target interaction prediction have been obtained by many effective computational models, both network-based and machine learning-based methods have their disadvantages, respectively. Furthermore, we discuss the future directions of the network-based drug discovery and network approach for personalized drug discovery based on personalized medicine, genome sequencing, tumor clone-based network and cancer hallmark-based network. Finally, we discussed the new evaluation validation framework and the formulation of drug-target interactions prediction problem by more realistic regression formulation based on quantitative bioactivity data.
引用
收藏
页码:696 / 712
页数:17
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