Tools for protein-protein interaction network analysis in cancer research

被引:31
|
作者
Sanz-Pamplona, Rebeca [1 ]
Berenguer, Antoni [1 ]
Sole, Xavier [1 ]
Cordero, David [1 ]
Crous-Bou, Marta [1 ]
Serra-Musach, Jordi [1 ]
Guino, Elisabet [1 ]
Angel Pujana, Miguel [1 ]
Moreno, Victor [1 ,2 ]
机构
[1] Biomed Res Ctr Network Epidemiol & Publ Hlth CIBE, Bellvitge Inst Biomed Res IDIBELL, Catalan Inst Oncol ICO, Unit Biomarkers & Susceptibil, ES-08908 Barcelona, Spain
[2] Univ Barcelona, Fac Med, Dept Clin Sci, Barcelona 7, Spain
来源
CLINICAL & TRANSLATIONAL ONCOLOGY | 2012年 / 14卷 / 01期
关键词
Cancer; Systems biology; Protein-protein interaction network; Public bioinformatics tools; Biomarker discovery; SYSTEMS BIOLOGY; SUBCELLULAR-LOCALIZATION; TOPOLOGICAL FEATURES; CYTOSCAPE PLUGIN; BUILDING-BLOCKS; GENE-EXPRESSION; DISEASE-GENES; IDENTIFICATION; VISUALIZATION; FRAMEWORK;
D O I
10.1007/s12094-012-0755-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As cancer is a complex disease, the representation of a malignant cell as a protein-protein interaction network (PPIN) and its subsequent analysis can provide insight into the behaviour of cancer cells and lead to the discovery of new biomarkers. The aim of this review is to help life-science researchers without previous computer programming skills to extract meaningful biological information from such networks, taking advantage of easyto-use, public bioinformatics tools. It is structured in four parts: the first section describes the pipeline of consecutive steps from network construction to biological hypothesis generation. The second part provides a repository of public, user-friendly tools for network construction, visualisation and analysis. Two different and complementary approaches of network analysis are presented: the topological approach studies the network as a whole by means of structural graph theory, whereas the global approach divides the PPIN into sub-graphs, or modules. In section three, some concepts and tools regarding heterogeneous molecular data integration through a PPIN are described. Finally, the fourth part is an example of how to extract meaningful biological information from a colorectal cancer PPIN using some of the described tools.
引用
收藏
页码:3 / 14
页数:12
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