Evidence map›Paper›PMID 26832302›Full record

ArticleScientific reports2016

Hierarchy of cellular decisions in collective behavior: Implications for wound healing.

Lisa E Wickert, Shaun Pomerenke, Isaiah Mitchell, Kristyn S Masters, Pamela K Kreeger

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 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
5.8field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  3. Review
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  9. Review
  10. Article
  11. Scaffold stiffness influences breast cancer cell invasion via EGFR-linked Mena upregulation and matrix remodeling.Matrix biology : journal of the International Society for Matrix Biology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Engineering Approaches to Study Cellular Decision Making.Annual review of biomedical engineering · 2018
    Review
  16. Article
  17. Immobilized epidermal growth factor stimulates persistent, directed keratinocyte migration via activation of PLCγ1.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    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

5 authors at 1 institution in 1 country.

Lisa E WickertDepartment of Biomedical Engineering, University of Wisconsin-Madison, 1550 Engineering Dr, Madison, WI, 53706 United States of America.
Shaun PomerenkeDepartment of Biomedical Engineering, University of Wisconsin-Madison, 1550 Engineering Dr, Madison, WI, 53706 United States of America.
Isaiah MitchellDepartment of Biomedical Engineering, University of Wisconsin-Madison, 1550 Engineering Dr, Madison, WI, 53706 United States of America.
Kristyn S MastersDepartment of Biomedical Engineering, University of Wisconsin-Madison, 1550 Engineering Dr, Madison, WI, 53706 United States of America.
Pamela K KreegerDepartment of Biomedical Engineering, University of Wisconsin-Madison, 1550 Engineering Dr, Madison, WI, 53706 United States of America.
University of Wisconsin–Madison · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Wendy M Kohrt · 1995 to 2026
$32.6M
Combinatorial analysis of migration stimuli for enhanced wound healingR01GM099031 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI MASTERS, KRISTYN S · 2011 to 2014
$1.1M
NIGMS NIH HHS R01 GM099031NIGMS NIH HHS R01-GM099031
6 · The paper itself

Abstract

Collective processes such as wound re-epithelialization result from the integration of individual cellular decisions. To determine which individual cell behaviors represent the most promising targets to engineer re-epithelialization, we examined collective and individual responses of HaCaT keratinocytes seeded upon polyacrylamide gels of three stiffnesses (1, 30, and 100 kPa) and treated with a range of epidermal growth factor (EGF) doses. Wound closure was found to increase with substrate stiffness, but was responsive to EGF treatment only above a stiffness threshold. Individual cell behaviors were used to create a partial least squares regression model to predict the hierarchy of factors driving wound closure. Unexpectedly, cell area and persistence were found to have the strongest correlation to the observed differences in wound closure. Meanwhile, the model predicted a relatively weak correlation between wound closure with proliferation, and the unexpectedly minor input from proliferation was successfully tested with inhibition by aphidicolin. Combined, these results suggest that the poor clinical results for growth factor-based therapies for chronic wounds may result from a disconnect between the individual cellular behaviors targeted in these approaches and the resulting collective response. Additionally, the stiffness-dependency of EGF sensitivity suggests that therapies matched to microenvironmental characteristics will be more efficacious.

Indexed as

Wound HealingCell AggregationCell LineCell MovementCell ProliferationEpidermal Growth FactorHumansKeratinocytesLeast-Squares AnalysisModels, BiologicalRegression AnalysisEpidermal Growth Factor

Identifiers

PMID26832302
PMCPMC4735862
OpenAlexW2418260809

What OpenQuestion holds

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LicenceCC BY
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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.