Systems biology, metabolic modelling and metabolomics in drug discovery and development

被引:204
作者
Kell, Douglas B.
机构
[1] Univ Manchester, Sch Chem, Manchester M60 1QD, Lancs, England
[2] Manchester Interdisciplinary Bioctr, Manchester Ctr Integrat Syst Biol, Manchester M1 7DN, Lancs, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
D O I
10.1016/j.drudis.2006.10.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Unlike signalling pathways, metabolic networks are subject to strict stoichiometric constraints. Metabolomics amplifies changes in the proteome, and represents more closely the phenotype of an organism. Recent advances enable the production (and computer-readable encoding as SBML) of metabolic network models reconstructed from genome sequences, as well as experimental measurements of much of the metabolome. There is increasing convergence between the number of human metabolites estimated via genomics (similar to 3000) and the number measured experimentally. It is thus both timely, and now possible, to bring these two approaches together as an integrated (if distributed) whole to help understand the genesis of metabolic biomarkers, the progress of disease, and the modes of action, efficacy, off-target effects and toxicity of pharmaceutical drugs.
引用
收藏
页码:1085 / 1092
页数:8
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