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本文引用的文献

1
Reduction of mathematical models of signal transduction networks: simulation-based approach applied to EGF receptor signalling.信号转导网络数学模型的简化:基于模拟的方法应用于表皮生长因子受体信号传导
Syst Biol (Stevenage). 2004 Jun;1(1):159-69. doi: 10.1049/sb:20045011.
2
Signal processing at the Ras circuit: what shapes Ras activation patterns?Ras信号通路中的信号处理:是什么塑造了Ras激活模式?
Syst Biol (Stevenage). 2004 Jun;1(1):104-13. doi: 10.1049/sb:20045003.
3
Simulation and sensitivity analysis of phosphorylation of EGFR signal transduction pathway in PC12 cell model.PC12细胞模型中表皮生长因子受体(EGFR)信号转导通路磷酸化的模拟与敏感性分析
Syst Biol (Stevenage). 2004 Dec;1(2):213-21. doi: 10.1049/sb:20045023.
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The statistical mechanics of complex signaling networks: nerve growth factor signaling.复杂信号网络的统计力学:神经生长因子信号传导
Phys Biol. 2004 Dec;1(3-4):184-95. doi: 10.1088/1478-3967/1/3/006.
5
In pursuit of systems.追求系统。
Nature. 2005 May 5;435(7038):1. doi: 10.1038/435001a.
6
Prediction and validation of the distinct dynamics of transient and sustained ERK activation.瞬时和持续ERK激活的不同动力学的预测与验证
Nat Cell Biol. 2005 Apr;7(4):365-73. doi: 10.1038/ncb1233. Epub 2005 Mar 27.
7
When kinases meet mathematics: the systems biology of MAPK signalling.当激酶遇上数学:丝裂原活化蛋白激酶信号传导的系统生物学
FEBS Lett. 2005 Mar 21;579(8):1891-5. doi: 10.1016/j.febslet.2005.02.002.
8
Hyperdigraph-theoretic analysis of the EGFR signaling network: initial steps leading to GTP:Ras complex formation.表皮生长因子受体(EGFR)信号网络的超图理论分析:导致GTP:Ras复合物形成的初始步骤。
J Comput Biol. 2004;11(5):812-42. doi: 10.1089/cmb.2004.11.812.
9
Cytoplasmic-to-nuclear volume ratio affects AP-1 complex formation as an indicator of cell cycle responsiveness.
FEBS Lett. 2005 Jan 17;579(2):433-40. doi: 10.1016/j.febslet.2004.11.104.
10
Principles behind the multifarious control of signal transduction. ERK phosphorylation and kinase/phosphatase control.信号转导多种调控背后的原理。细胞外调节蛋白激酶磷酸化及激酶/磷酸酶调控。
FEBS J. 2005 Jan;272(1):244-58. doi: 10.1111/j.1432-1033.2004.04404.x.

受体酪氨酸激酶激活的丝裂原活化蛋白激酶途径的计算建模

Computational modelling of the receptor-tyrosine-kinase-activated MAPK pathway.

作者信息

Orton Richard J, Sturm Oliver E, Vyshemirsky Vladislav, Calder Muffy, Gilbert David R, Kolch Walter

机构信息

Bioinformatics Research Centre, Department of Computing Science, University of Glasgow, Glasgow G12 8QQ, Scotland, UK.

出版信息

Biochem J. 2005 Dec 1;392(Pt 2):249-61. doi: 10.1042/BJ20050908.

DOI:10.1042/BJ20050908
PMID:16293107
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1316260/
Abstract

The MAPK (mitogen-activated protein kinase) pathway is one of the most important and intensively studied signalling pathways. It is at the heart of a molecular-signalling network that governs the growth, proliferation, differentiation and survival of many, if not all, cell types. It is de-regulated in various diseases, ranging from cancer to immunological, inflammatory and degenerative syndromes, and thus represents an important drug target. Over recent years, the computational or mathematical modelling of biological systems has become increasingly valuable, and there is now a wide variety of mathematical models of the MAPK pathway which have led to some novel insights and predictions as to how this system functions. In the present review we give an overview of the processes involved in modelling a biological system using the popular approach of ordinary differential equations. Focusing on the MAPK pathway, we introduce the features and functions of the pathway itself before comparing the available models and describing what new biological insights they have led to.

摘要

丝裂原活化蛋白激酶(MAPK)信号通路是最重要且研究最深入的信号通路之一。它处于一个分子信号网络的核心位置,该网络控制着许多(即便不是所有)细胞类型的生长、增殖、分化和存活。在从癌症到免疫、炎症和退行性综合征等各种疾病中,它都发生了失调,因此是一个重要的药物靶点。近年来,生物系统的计算或数学建模变得越来越有价值,现在有各种各样的MAPK信号通路数学模型,这些模型对该系统的功能产生了一些新颖的见解和预测。在本综述中,我们概述了使用常微分方程这种流行方法对生物系统进行建模所涉及的过程。以MAPK信号通路为重点,我们先介绍该信号通路本身的特征和功能,然后比较现有的模型,并描述它们带来了哪些新的生物学见解。