Fuzzy Logic Analysis of Kinase Pathway Crosstalk in TNF/EGF/Insulin-Induced Signaling

被引:104
作者
Aldridge, Bree B. [1 ,2 ,3 ]
Saez-Rodriguez, Julio [1 ,2 ,3 ]
Muhlich, Jeremy L. [1 ,3 ]
Sorger, Peter K. [1 ,2 ,3 ]
Lauffenburger, Douglas A. [1 ,2 ,3 ]
机构
[1] Ctr Cell Decis Proc, Cambridge, MA USA
[2] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[3] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
关键词
GENE-EXPRESSION DATA; REGULATORY NETWORKS; EPITHELIAL-CELLS; SYSTEMS BIOLOGY; GROWTH; MODELS; DYNAMICS; DIFFERENTIATION; TRANSDUCTION; ENDOCYTOSIS;
D O I
10.1371/journal.pcbi.1000340
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
When modeling cell signaling networks, a balance must be struck between mechanistic detail and ease of interpretation. In this paper we apply a fuzzy logic framework to the analysis of a large, systematic dataset describing the dynamics of cell signaling downstream of TNF, EGF, and insulin receptors in human colon carcinoma cells. Simulations based on fuzzy logic recapitulate most features of the data and generate several predictions involving pathway crosstalk and regulation. We uncover a relationship between MK2 and ERK pathways that might account for the previously identified pro-survival influence of MK2. We also find unexpected inhibition of IKK following EGF treatment, possibly due to down-regulation of autocrine signaling. More generally, fuzzy logic models are flexible, able to incorporate qualitative and noisy data, and powerful enough to produce quantitative predictions and new biological insights about the operation of signaling networks.
引用
收藏
页数:13
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