From protein interaction networks to novel therapeutic strategies

被引:37
|
作者
Jaeger, Samira [1 ]
Aloy, Patrick [1 ,2 ]
机构
[1] Biomed Res Inst, Joint IRB BSC Program Computat Biol, Barcelona 08028, Spain
[2] ICREA, Barcelona, Spain
关键词
protein networks; network medicine; polypharmacology; drug repositioning; drug cocktails; DISEASE-GENES; TOPOLOGICAL FEATURES; FUNCTIONAL MODULES; P53; TARGET; YEAST; ANNOTATION; SEQUENCE; PRIORITIZATION; IDENTIFICATION;
D O I
10.1002/iub.1040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cellular mechanisms that sustain health or contribute to disease emerge mostly from the complex interplay among various molecular entities. To understand the underlying relationships between genotype, environment and phenotype, one has to consider the intricate and nonsequential interaction patterns formed between the different sets of cellular players. Biological networks capture a variety of molecular interactions and thus provide an excellent opportunity to consider physiological characteristics of individual molecules within their cellular context. In particular, the concept of network biology and its applications contributed largely to recent advances in biomedical research. In this review, we show (i) how biological networks, i.e., proteinprotein interaction networks, facilitate the understanding of pathogenic mechanisms that trigger the onset and progression of diseases and (ii) how this knowledge can be translated into effective diagnostic and therapeutic strategies. In particular, we focus on the impact of network pharmacological concepts that go beyond the classical view on individual drugs and targets aiming for combinational therapies with improved clinical efficacy and reduced safety risks. (C) 2012 IUBMB Life, 2012
引用
收藏
页码:529 / 537
页数:9
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