Uniformly curated signaling pathways reveal tissue-specific cross-talks and support drug target discovery

被引:60
作者
Korcsmaros, Tamas [1 ,2 ]
Farkas, Illes J. [3 ]
Szalay, Mate S. [1 ]
Rovo, Petra [2 ]
Fazekas, David [2 ]
Spiro, Zoltan [1 ]
Bode, Csaba [4 ]
Lenti, Katalin [5 ]
Vellai, Tibor [2 ]
Csermely, Peter [1 ]
机构
[1] Semmelweis Univ, Dept Med Chem, H-1444 Budapest, Hungary
[2] Eotvos Lorand Univ, Dept Genet, H-1117 Budapest, Hungary
[3] Hungarian Acad Sci, Stat & Biol Phys Grp, H-1117 Budapest, Hungary
[4] Morgan Stanley Hungary Analyt Ltd, H-1095 Budapest, Hungary
[5] Semmelweis Univ, Dept Morphol & Physiol, H-1088 Budapest, Hungary
关键词
NETWORKS; EVOLUTION; DATABASE; GENES; RESOURCE; BIOLOGY; SEARCH; CANCER; TERMS; ROR2;
D O I
10.1093/bioinformatics/btq310
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Signaling pathways control a large variety of cellular processes. However, currently, even within the same database signaling pathways are often curated at different levels of detail. This makes comparative and cross-talk analyses difficult. Results: We present SignaLink, a database containing eight major signaling pathways from Caenorhabditis elegans, Drosophila melanogaster and humans. Based on 170 review and similar to 800 research articles, we have compiled pathways with semi-automatic searches and uniform, well-documented curation rules. We found that in humans any two of the eight pathways can cross-talk. We quantified the possible tissue-and cancer-specific activity of cross-talks and found pathway-specific expression profiles. In addition, we identified 327 proteins relevant for drug target discovery. Conclusions: We provide a novel resource for comparative and cross-talk analyses of signaling pathways. The identified multi-pathway and tissue-specific cross-talks contribute to the understanding of the signaling complexity in health and disease, and underscore its importance in network-based drug target selection.
引用
收藏
页码:2042 / 2050
页数:9
相关论文
共 56 条
[1]   McKusick's Online Mendelian Inheritance in Man (OMIM®) [J].
Amberger, Joanna ;
Bocchini, Carol A. ;
Scott, Alan F. ;
Hamosh, Ada .
NUCLEIC ACIDS RESEARCH, 2009, 37 :D793-D796
[2]   Pathguide: a Pathway Resource List [J].
Bader, Gary D. ;
Cary, Michael P. ;
Sander, Chris .
NUCLEIC ACIDS RESEARCH, 2006, 34 :D504-D506
[3]   Analyzing yeast protein-protein interaction data obtained from different sources [J].
Bader, GD ;
Hogue, CWV .
NATURE BIOTECHNOLOGY, 2002, 20 (10) :991-997
[4]   Pathway databases and tools for their exploitation: benefits, current limitations and challenges [J].
Bauer-Mehren, Anna ;
Furlong, Laura I. ;
Sanz, Ferran .
MOLECULAR SYSTEMS BIOLOGY, 2009, 5
[5]  
Becker KG, 2004, NAT GENET, V36, P431, DOI 10.1038/ng0504-431
[6]   Kinetic insulation as an effective mechanism for achieving pathway specificity in intracellular signaling networks [J].
Behar, Marcelo ;
Dohlman, Henrik G. ;
Elston, Timothy C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (41) :16146-16151
[7]   Network analyses in systems pharmacology [J].
Berger, Seth I. ;
Iyengar, Ravi .
BIOINFORMATICS, 2009, 25 (19) :2466-2472
[8]   InParanoid 6:: eukaryotic ortholog clusters with inparalogs [J].
Berglund, Ann-Charlotte ;
Sjolund, Erik ;
Ostlund, Gabriel ;
Sonnhammer, Erik L. L. .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D263-D266
[9]   Integrating physical and genetic maps: from genomes to interaction networks [J].
Beyer, Andreas ;
Bandyopadhyay, Sourav ;
Ideker, Trey .
NATURE REVIEWS GENETICS, 2007, 8 (09) :699-710
[10]   Domains, motifs, and scaffolds:: The role of modular interactions in the evolution and wiring of cell signaling circuits [J].
Bhattacharyya, Roby P. ;
Remenyi, Attila ;
Yeh, Brian J. ;
Lim, Wendell A. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2006, 75 :655-680