Evidence map›Paper›PMID 28336062›Full record

ArticleMethods in enzymology2017

Integrated Strategies to Gain a Systems-Level View of Dynamic Signaling Networks.

Robert H Newman, Jin Zhang

Abstract read
In one paragraph

Article in Methods in enzymology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
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

2 authors.

Robert H NewmanNorth Carolina Agricultural and Technical State University, Greensboro, NC, United States. Electronic address: rhnewman@ncat.edu.
Jin ZhangUniversity of California, San Diego, San Diego, CA, United States. Electronic address: jzhang32@ucsd.edu.

Funding

Live-cell Activity Architecture in CancerR35CA197622 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Jin Zhang · 2015 to 2026
$11.2M
Mechanisms of Compartmentalized cAMP SignalingR01DK073368 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Jin Zhang · 2006 to 2026
$7.6M
Multiplex in vivo imaging of cell-specific and circuit-specific signaling pathways during synaptic plasticityR01MH111516 · NIMH · JOHNS HOPKINS UNIVERSITY · PI HUGANIR, RICHARD L, ZHANG, JIN · 2016 to 2018
$1.8M
Signal Transduction by PI3K/Akt/mTOR PathwayR01GM111665 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHANG, JIN · 2015 to 2018
$1.2M
Global Analysis of Redox Modification on Protein Kinase FunctionSC2GM113784 · NIGMS · NORTH CAROLINA AGRI & TECH ST UNIV · PI NEWMAN, ROBERT HOWARD · 2015 to 2017
$346k
NCI NIH HHS R35 CA197622NIDDK NIH HHS R01 DK073368NIGMS NIH HHS R01 GM111665NIGMS NIH HHS SC2 GM113784NIMH NIH HHS R01 MH111516
6 · The paper itself

Abstract

In order to survive and function properly in the face of an ever changing environment, cells must be able to sense changes in their surroundings and respond accordingly. Cells process information about their environment through complex signaling networks composed of many discrete signaling molecules. Individual pathways within these networks are often tightly integrated and highly dynamic, allowing cells to respond to a given stimulus (or, as is typically the case under physiological conditions, a combination of stimuli) in a specific and appropriate manner. However, due to the size and complexity of many cellular signaling networks, it is often difficult to predict how cellular signaling networks will respond under a particular set of conditions. Indeed, crosstalk between individual signaling pathways may lead to responses that are nonintuitive (or even counterintuitive) based on examination of the individual pathways in isolation. Therefore, to gain a more comprehensive view of cell signaling processes, it is important to understand how signaling networks behave at the systems level. This requires integrated strategies that combine quantitative experimental data with computational models. In this chapter, we first examine some of the progress that has recently been made toward understanding the systems-level regulation of cellular signaling networks, with a particular emphasis on phosphorylation-dependent signaling networks. We then discuss how genetically targetable fluorescent biosensors are being used together with computational models to gain unique insights into the spatiotemporal regulation of signaling networks within single, living cells.

Indexed as

Protein Interaction MapsSignal TransductionAnimalsBiosensing TechniquesComputer SimulationFlow CytometryHumansMass SpectrometryPhosphoric Monoester HydrolasesPhosphorylationProtein Array AnalysisProtein Interaction MappingProtein KinasesProteinsProteomicsSystems BiologyPhosphoric Monoester HydrolasesProtein KinasesProteinsComputational modelFluorescent biosensorMass cytometryMass spectrometryPhosphoproteomicsPhosphorylation networkProtein kinaseProtein microarraySignaling networkSystems biology

Identifiers

PMID28336062
PMCPMC6014622

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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.