Evidence map›Paper›PMID 27662842›Full record

ArticleBMC systems biology2016

Identification of control targets in Boolean molecular network models via computational algebra.

David Murrugarra, Alan Veliz-Cuba, Boris Aguilar, Reinhard Laubenbacher

Abstract read
In one paragraph

Article in BMC systems biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Modularity of biological systems: a link between structure and function.bioRxiv : the preprint server for biology · 2023
    Article
  6. Review
  7. Phenotype control techniques for Boolean gene regulatory networks.bioRxiv : the preprint server for biology · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Qualitative Modeling, Analysis and Control of Synthetic Regulatory Circuits.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Molecular network control through boolean canalization.EURASIP journal on bioinformatics & systems biology · 2015
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

David MurrugarraDepartment of Mathematics, University of Kentucky, Lexington, 40506-0027, KY, USA. murrugarra@uky.edu.
Alan Veliz-CubaDepartment of Mathematics, University of Dayton, Dayton, 45469, OH, USA.
Boris AguilarInstitute for Systems Biology, Seattle, 98109-5263, WA, USA.
Reinhard LaubenbacherCenter for Quantitative Medicine, University of Connecticut Health Center, Farmington, 06030-6033, CT, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany problems in biomedicine and other areas of the life sciences can be characterized as control problems, with the goal of finding strategies to change a disease or otherwise undesirable state of a biological system into another, more desirable, state through an intervention, such as a drug or other therapeutic treatment. The identification of such strategies is typically based on a mathematical model of the process to be altered through targeted control inputs. This paper focuses on processes at the molecular level that determine the state of an individual cell, involving signaling or gene regulation. The mathematical model type considered is that of Boolean networks. The potential control targets can be represented by a set of nodes and edges that can be manipulated to produce a desired effect on the system.

resultsThis paper presents a method for the identification of potential intervention targets in Boolean molecular network models using algebraic techniques. The approach exploits an algebraic representation of Boolean networks to encode the control candidates in the network wiring diagram as the solutions of a system of polynomials equations, and then uses computational algebra techniques to find such controllers. The control methods in this paper are validated through the identification of combinatorial interventions in the signaling pathways of previously reported control targets in two well studied systems, a p53-mdm2 network and a blood T cell lymphocyte granular leukemia survival signaling network. Supplementary data is available online and our code in Macaulay2 and Matlab are available via http://www.ms.uky.edu/~dmu228/ControlAlg .

conclusionsThis paper presents a novel method for the identification of intervention targets in Boolean network models. The results in this paper show that the proposed methods are useful and efficient for moderately large networks.

Indexed as

Algebraic controlBlocking transitionsBoolean networksEdge deletionsNetwork control

Identifiers

PMID27662842
PMCPMC5035508

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Registered trials

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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.