ArticleBMC systems biology2008
Dynamical modeling of the cholesterol regulatory pathway with Boolean networks.
Article in BMC systems biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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15 citing papers in PubMed, 40 citations in OpenAlex.
- Boolean-network simplification and rule fitting to unravel chemotherapy resistance in non-small cell lung cancer.PloS one · 2026Article
- Insights on TAM Formation from a Boolean Model of Macrophage Polarization Based on In Vitro Studies.Cancers · 2020Article
- Cholesterol Homeostasis: An In Silico Investigation into How Aging Disrupts Its Key Hepatic Regulatory Mechanisms.Biology · 2020Article
- Identification of Biologically Essential Nodes via Determinative Power in Logical Models of Cellular Processes.Frontiers in physiology · 2018Article
- A Boolean network of the crosstalk between IGF and Wnt signaling in aging satellite cells.PloS one · 2018Article
- A new discrete dynamic model of ABA-induced stomatal closure predicts key feedback loops.PLoS biology · 2017Article
- Cytochrome P450 metabolism of the post-lanosterol intermediates explains enigmas of cholesterol synthesis.Scientific reports · 2016Article
- An algebra-based method for inferring gene regulatory networks.BMC systems biology · 2014Article
- Learning contextual gene set interaction networks of cancer with condition specificity.BMC genomics · 2013Article
- A physiologically based in silico kinetic model predicting plasma cholesterol concentrations in humans.Journal of lipid research · 2012Article
- A whole-body mathematical model of cholesterol metabolism and its age-associated dysregulation.BMC systems biology · 2012Article
- Stochastic Boolean networks: an efficient approach to modeling gene regulatory networks.BMC systems biology · 2012Article
- Dynamical systems approach to endothelial heterogeneity.Circulation research · 2012Review
- Dynamical and structural analysis of a T cell survival network identifies novel candidate therapeutic targets for large granular lymphocyte leukemia.PLoS computational biology · 2011Article
- Adapted Boolean network models for extracellular matrix formation.BMC systems biology · 2009Article
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Authors and funding
2 authors at 1 institution in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundQualitative dynamics of small gene regulatory networks have been studied in quite some details both with synchronous and asynchronous analysis. However, both methods have their drawbacks: synchronous analysis leads to spurious attractors and asynchronous analysis lacks computational efficiency, which is a problem to simulate large networks. We addressed this question through the analysis of a major biosynthesis pathway. Indeed the cholesterol synthesis pathway plays a pivotal role in dislypidemia and, ultimately, in cancer through intermediates such as mevalonate, farnesyl pyrophosphate and geranyl geranyl pyrophosphate, but no dynamic model of this pathway has been proposed until now.
resultsWe set up a computational framework to dynamically analyze large biological networks. This framework associates a classical and computationally efficient synchronous Boolean analysis with a newly introduced method based on Markov chains, which identifies spurious cycles among the results of the synchronous simulation. Based on this method, we present here the results of the analysis of the cholesterol biosynthesis pathway and its physiological regulation by the Sterol Response Element Binding Proteins (SREBPs), as well as the modeling of the action of statins, inhibitor drugs, on this pathway. The in silico experiments show the blockade of the cholesterol endogenous synthesis by statins and its regulation by SREPBs, in full agreement with the known biochemical features of the pathway.
conclusionWe believe that the method described here to identify spurious cycles opens new routes to compute large and biologically relevant models, thanks to the computational efficiency of synchronous simulation. Furthermore, to the best of our knowledge, we present here the first dynamic systems biology model of the human cholesterol pathway and several of its key regulatory control elements, hoping it would provide a good basis to perform in silico experiments and confront the resulting properties with published and experimental data. The model of the cholesterol pathway and its regulation, along with Boolean formulae used for simulation are available on our web site http://Bioinformaticsu613.free.fr. Graphical results of the simulation are also shown online. The SBML model is available in the BioModels database http://www.ebi.ac.uk/biomodels/ with submission ID: MODEL0568648427.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.