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Fuzzy Logic Analysis of Kinase Pathway Crosstalk in TNF/EGF/Insulin-Induced Signaling
Author(s) -
Bree B. Aldridge,
Julio Sáez-Rodríguez,
Jeremy Muhlich,
Peter K. Sorger,
Douglas A. Lauffenburger
Publication year - 2009
Publication title -
plos computational biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.628
H-Index - 182
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.1000340
Subject(s) - crosstalk , fuzzy logic , autocrine signalling , signal transduction , insulin receptor , biology , mapk/erk pathway , computer science , computational biology , microbiology and biotechnology , bioinformatics , receptor , insulin , artificial intelligence , insulin resistance , electronic engineering , genetics , engineering , endocrinology
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.

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