Evidence map›Paper›PMID 24824602›Full record

ArticlePloS one2014

A data-driven, mathematical model of mammalian cell cycle regulation.

Michael C Weis, Jayant Avva, James W Jacobberger, Sree N Sreenath

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
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

12 citing papers in PubMed, 39 citations in OpenAlex.

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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 at 1 institution in 1 country.

Michael C WeisDepartment of Electrical Engineering and Computer Science, Case Western Reserve University, Cleveland, Ohio, United States of America.
Jayant AvvaDepartment of Electrical Engineering and Computer Science, Case Western Reserve University, Cleveland, Ohio, United States of America.
James W JacobbergerCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, Ohio, United States of America.
Sree N SreenathDepartment of Electrical Engineering and Computer Science, Case Western Reserve University, Cleveland, Ohio, United States of America.
Case Western Reserve University · US

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARK R CHANCE · 1987 to 2026
$142.3M
STANDARDIZED MULTIPARAMETRIC CELL CYCLE ANALYSISR01CA073413 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI JACOBBERGER, JAMES W · 1996 to 2008
$2.4M
NCI NIH HHS P30 CA043703NCI NIH HHS P30CA43703NCI NIH HHS R01 CA073413NCI NIH HHS R01CA73413
6 · The paper itself

Abstract

Few of >150 published cell cycle modeling efforts use significant levels of data for tuning and validation. This reflects the difficultly to generate correlated quantitative data, and it points out a critical uncertainty in modeling efforts. To develop a data-driven model of cell cycle regulation, we used contiguous, dynamic measurements over two time scales (minutes and hours) calculated from static multiparametric cytometry data. The approach provided expression profiles of cyclin A2, cyclin B1, and phospho-S10-histone H3. The model was built by integrating and modifying two previously published models such that the model outputs for cyclins A and B fit cyclin expression measurements and the activation of B cyclin/Cdk1 coincided with phosphorylation of histone H3. The model depends on Cdh1-regulated cyclin degradation during G1, regulation of B cyclin/Cdk1 activity by cyclin A/Cdk via Wee1, and transcriptional control of the mitotic cyclins that reflects some of the current literature. We introduced autocatalytic transcription of E2F, E2F regulated transcription of cyclin B, Cdc20/Cdh1 mediated E2F degradation, enhanced transcription of mitotic cyclins during late S/early G2 phase, and the sustained synthesis of cyclin B during mitosis. These features produced a model with good correlation between state variable output and real measurements. Since the method of data generation is extensible, this model can be continually modified based on new correlated, quantitative data.

Indexed as

Models, BiologicalAntigens, CDCadherinsCell CycleComputer SimulationCyclin ACyclin B1CyclinsE2F Transcription FactorsHumansK562 CellsMitosisTime FactorsTranscriptomeAntigens, CDCadherinsCDH1 protein, humanCyclin ACyclin B1CyclinsE2F Transcription Factors

Identifiers

PMID24824602
PMCPMC4019653
OpenAlexW2091841161

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.