Evidence map›Paper›PMID 26778564›Full record

ReviewMethods in enzymology2016

In Vitro Model of the Epidermis: Connecting Protein Function to 3D Structure.

Christopher Arnette, Jennifer L Koetsier, Paul Hoover, Spiro Getsios, Kathleen J Green

Abstract readReview
In one paragraph

Review in Methods in enzymology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
–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

47 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Advances in Microengineered Platforms for Skin Research.JID innovations : skin science from molecules to population health · 2025
    Review
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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

5 authors.

Christopher ArnetteDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Jennifer L KoetsierDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Paul HooverDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Spiro GetsiosDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois, USA.
Kathleen J GreenDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois, USA. Electronic address: kgreen@northwestern.edu.

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
MOLECULAR GENETICS OF PEMPHIGUS FOLIACEUS ANTIGENR01AR041836 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Kathleen Janee Green · 1993 to 2026
$11.8M
The Role of Keratinocytes as Independent ThermosensorsP30AR057216 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PALLER, AMY S · 2009 to 2018
$6.0M
Desmoplakin Assembly and Function in EpidermisR37AR043380 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GREEN, KATHLEEN JANEE · 2011 to 2020
$4.6M
Regulation of Desmosomal Cadherins in Oral CancerR01CA122151 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GREEN, KATHLEEN JANEE · 2006 to 2016
$2.6M
EphA/Ephrin-A signaling in epidermal differentiation and diseaseR01AR062110 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LAVKER, ROBERT M · 2012 to 2016
$1.9M
NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA122151NIAMS NIH HHS P30 AR057216NIAMS NIH HHS R01 AR041836NIAMS NIH HHS R01 AR062110NIAMS NIH HHS R37 AR043380
6 · The paper itself

Abstract

Much of our understanding of the biological processes that underlie cellular functions in humans, such as cell-cell communication, intracellular signaling, and transcriptional and posttranscriptional control of gene expression, has been acquired from studying cells in a two-dimensional (2D) tissue culture environment. However, it has become increasingly evident that the 2D environment does not support certain cell functions. The need for more physiologically relevant models prompted the development of three-dimensional (3D) cultures of epithelial, endothelial, and neuronal tissues (Shamir & Ewald, 2014). These models afford investigators with powerful tools to study the contribution of spatial organization, often in the context of relevant extracellular matrix and stromal components, to cellular and tissue homeostasis in normal and disease states.

Indexed as

3T3 CellsAnimalsCell Culture TechniquesEpidermal CellsEpidermisGene ExpressionGene Knockdown TechniquesHumansKeratinocytesMiceModels, BiologicalDesmogleinEpidermisKeratinocyteOrganotypic

Identifiers

PMID26778564
PMCPMC4870045

What OpenQuestion holds

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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.