Combining Drug and Gene Similarity Measures for Drug-Target Elucidation

被引:213
作者
Perlman, Liat [1 ]
Gottlieb, Assaf [1 ]
Atias, Nir [1 ]
Ruppin, Eytan [1 ,2 ]
Sharan, Roded [1 ]
机构
[1] Tel Aviv Univ, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Sch Med, IL-69978 Tel Aviv, Israel
关键词
computational molecular biology; gene expression; gene networks; genetic variation; machine learning; sequence analysis; EXPRESSION; PREDICTION; NETWORKS; PROTEINS; DATABASE; MODEL; TOOL; KNOWLEDGEBASE; MOLECULES; ONTOLOGY;
D O I
10.1089/cmb.2010.0213
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Understanding drugs and their modes of action is a fundamental challenge in systems medicine. Key to addressing this challenge is the elucidation of drug targets, an important step in the search for new drugs or novel targets for existing drugs. Incorporating multiple biological information sources is of essence for improving the accuracy of drug target prediction. In this article, we introduce a novel framework-Similarity-based Inference of drug-TARgets (SITAR)-for incorporating multiple drug-drug and gene-gene similarity measures for drug target prediction. The framework consists of a new scoring scheme for drug-gene associations based on a given pair of drug-drug and gene-gene similarity measures, combined with a logistic regression component that integrates the scores of multiple measures to yield the final association score. We apply our framework to predict targets for hundreds of drugs using both commonly used and novel drug-drug and gene-gene similarity measures and compare our results to existing state of the art methods, markedly outperforming them. We then employ our framework to make novel target predictions for hundreds of drugs; we validate these predictions via curated databases that were not used in the learning stage. Our framework provides an extensible platform for incorporating additional emerging similarity measures among drugs and genes. Supplementary Material is available at www.liebertonline.com/cmb.
引用
收藏
页码:133 / 145
页数:13
相关论文
共 64 条
[1]
[Anonymous], 2006, MDL DRUG DAT REP
[2]
Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[3]
Atias N., 2010, RECOMB 2010 IN PRESS
[4]
Supervised prediction of drug-target interactions using bipartite local models [J].
Bleakley, Kevin ;
Yamanishi, Yoshihiro .
BIOINFORMATICS, 2009, 25 (18) :2397-2403
[5]
The BioGRID interaction database:: 2008 update [J].
Breitkreutz, Bobby-Joe ;
Stark, Chris ;
Reguly, Teresa ;
Boucher, Lorrie ;
Breitkreutz, Ashton ;
Livstone, Michael ;
Oughtred, Rose ;
Lackner, Daniel H. ;
Bahler, Jurg ;
Wood, Valerie ;
Dolinski, Kara ;
Tyers, Mike .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D637-D640
[6]
Calreticulin inhibits glucocorticoid- but not cAMP-sensitive expression of tyrosine aminotransferase gene in cultured McA-RH7777 hepatocytes [J].
Burns, K ;
Opas, M ;
Michalak, M .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1997, 171 (1-2) :37-43
[7]
Drug target identification using side-effect similarity [J].
Campillos, Monica ;
Kuhn, Michael ;
Gavin, Anne-Claude ;
Jensen, Lars Juhl ;
Bork, Peer .
SCIENCE, 2008, 321 (5886) :263-266
[8]
LIBSVM: A Library for Support Vector Machines [J].
Chang, Chih-Chung ;
Lin, Chih-Jen .
ACM TRANSACTIONS ON INTELLIGENT SYSTEMS AND TECHNOLOGY, 2011, 2 (03)
[9]
Minocycline inhibits caspase-1 and caspase-3 expression and delays mortality in a transgenic mouse model of Huntington disease [J].
Chen, M ;
Ona, VO ;
Li, MW ;
Ferrante, RJ ;
Fink, KB ;
Zhu, S ;
Bian, J ;
Guo, L ;
Farrell, LA ;
Hersch, SM ;
Hobbs, W ;
Vonsattel, JP ;
Cha, JHJ ;
Friedlander, RM .
NATURE MEDICINE, 2000, 6 (07) :797-+
[10]
Structure-based maximal affinity model predicts small-molecule druggability [J].
Cheng, Alan C. ;
Coleman, Ryan G. ;
Smyth, Kathleen T. ;
Cao, Qing ;
Soulard, Patricia ;
Caffrey, Daniel R. ;
Salzberg, Anna C. ;
Huang, Enoch S. .
NATURE BIOTECHNOLOGY, 2007, 25 (01) :71-75