Evidence map›Paper›PMID 25862149›Full record

ArticleJournal of dermatological science2015

Quantitative proteogenomic profiling of epidermal barrier formation in vitro.

Jason M Winget, Julian D Watts, Michael R Hoopmann, Teresa DiColandrea, Michael K Robinson, Tom Huggins, Charles C Bascom, Robert J Isfort, Robert L Moritz

Abstract read
In one paragraph

Article in Journal of dermatological science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 94% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 2 institutions in 1 country.

Jason M WingetInstitute for Systems Biology, 401 Terry Ave N., Seattle, WA 98109, USA.
Julian D WattsInstitute for Systems Biology, 401 Terry Ave N., Seattle, WA 98109, USA.
Michael R HoopmannInstitute for Systems Biology, 401 Terry Ave N., Seattle, WA 98109, USA.
Teresa DiColandreaThe Procter & Gamble Company, Mason Business Center, Cincinnati, OH 45040, USA.
Michael K RobinsonThe Procter & Gamble Company, Mason Business Center, Cincinnati, OH 45040, USA.
Tom HugginsThe Procter & Gamble Company, Mason Business Center, Cincinnati, OH 45040, USA.
Charles C BascomThe Procter & Gamble Company, Mason Business Center, Cincinnati, OH 45040, USA.
Robert J IsfortThe Procter & Gamble Company, Mason Business Center, Cincinnati, OH 45040, USA.
Robert L MoritzInstitute for Systems Biology, 401 Terry Ave N., Seattle, WA 98109, USA. Electronic address: rmoritz@systemsbiology.org.
Procter & Gamble (United States) · USInstitute for Systems Biology · US

Funding

Quantitative Systems BiologyP50GM076547 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI BALIGA, NITIN S · 2006 to 2016
$30.6M
Shortening the development cycle time of Trans Proteomic Pipeline tools with high performance computingR01GM087221 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI DEUTSCH, ERIC, MORITZ, ROBERT L · 2010 to 2021
$6.0M
FAIMS-Selected Reaction Monitoring to Quantitative Protein Networks in DiseaseS10RR027584 · NCRR · INSTITUTE FOR SYSTEMS BIOLOGY · PI MORITZ, ROBERT L · 2011 to 2011
$576k
NCRR NIH HHS S10 RR027584NCRR NIH HHS S10RR027584NIGMS NIH HHS 2P50 GM076547NIGMS NIH HHS GM087221NIGMS NIH HHS P50 GM076547NIGMS NIH HHS R01 GM087221
6 · The paper itself

Abstract

backgroundThe barrier function of the epidermis is integral to personal well-being, and defects in the skin barrier are associated with several widespread diseases. Currently there is a limited understanding of system-level proteomic changes during epidermal stratification and barrier establishment.

objectiveHere we report the quantitative proteogenomic profile of an in vitro reconstituted epidermis at three time points of development in order to characterize protein changes during stratification.

methodsThe proteome was measured using data-dependent "shotgun" mass spectrometry and quantified with statistically validated label-free proteomic methods for 20 replicates at each of three time points during the course of epidermal development.

resultsOver 3600 proteins were identified in the reconstituted epidermis, with more than 1200 of these changing in abundance over the time course. We also collected and discuss matched transcriptomic data for the three time points, allowing alignment of this new dataset with previously published characterization of the reconstituted epidermis system.

conclusionThese results represent the most comprehensive epidermal-specific proteome to date, and therefore reveal several aspects of barrier formation and skin composition. The limited correlation between transcript and protein abundance underscores the importance of proteomic analysis in developing a full understanding of epidermal maturation.

Indexed as

ProteomicsEpidermisHumansIn Vitro TechniquesPilot ProjectsTight JunctionsTranscriptomeBarrierEpidermal differentiationProteomicsSkin equivalent

Identifiers

PMID25862149
PMCPMC4424144
OpenAlexW2090598584

What OpenQuestion holds

Textmetadata
LicenceTDM
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.