Evidence map›Paper›PMID 26057128›Full record

ArticlePloS one2015

Epidermal Growth Factor Removal or Tyrphostin AG1478 Treatment Reduces Goblet Cells & Mucus Secretion of Epithelial Cells from Asthmatic Children Using the Air-Liquid Interface Model.

Jeremy C Parker, Isobel Douglas, Jennifer Bell, David Comer, Keith Bailie, Grzegorz Skibinski, Liam G Heaney, Michael D Shields

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Characterizing well-differentiated culture of primary human nasal epithelial cells for use in wound healing assays.Laboratory investigation; a journal of technical methods and pathology · 2018
    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

8 authors at 1 institution in 1 country.

Jeremy C ParkerCentre for Infection and Immunity, Health Sciences Building, Queen's University Belfast, Belfast, Northern Ireland.
Isobel DouglasRoyal Belfast Hospital for Sick Children, Belfast, Northern Ireland.
Jennifer BellCentre for Infection and Immunity, Health Sciences Building, Queen's University Belfast, Belfast, Northern Ireland.
David ComerCentre for Infection and Immunity, Health Sciences Building, Queen's University Belfast, Belfast, Northern Ireland.
Keith BailieRoyal Belfast Hospital for Sick Children, Belfast, Northern Ireland.
Grzegorz SkibinskiCentre for Infection and Immunity, Health Sciences Building, Queen's University Belfast, Belfast, Northern Ireland.
Liam G HeaneyCentre for Infection and Immunity, Health Sciences Building, Queen's University Belfast, Belfast, Northern Ireland.
Michael D ShieldsCentre for Infection and Immunity, Health Sciences Building, Queen's University Belfast, Belfast, Northern Ireland; Royal Belfast Hospital for Sick Children, Belfast, Northern Ireland.
Queen's University Belfast · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleEpithelial remodelling in asthma is characterised by goblet cell hyperplasia and mucus hypersecretion for which no therapies exist. Differentiated bronchial air-liquid interface cultures from asthmatic children display high goblet cell numbers. Epidermal growth factor and its receptor have been implicated in goblet cell hyperplasia.

objectivesWe hypothesised that EGF removal or tyrphostin AG1478 treatment of differentiating air-liquid interface cultures from asthmatic children would result in a reduction of epithelial goblet cells and mucus secretion.

methodsIn Aim 1 primary bronchial epithelial cells from non-asthmatic (n = 5) and asthmatic (n = 5) children were differentiated under EGF-positive (10 ng/ml EGF) and EGF-negative culture conditions for 28 days. In Aim 2, cultures from a further group of asthmatic children (n = 5) were grown under tyrphostin AG1478, a tyrosine kinase inhibitor, conditions. All cultures were analysed for epithelial resistance, markers of differentiation using immunocytochemistry, ELISA for MUC5AC mucin secretion and qPCR for MUC5AC mRNA.

resultsIn cultures from asthmatic children the goblet cell number was reduced in the EGF negative group (p = 0.01). Tyrphostin AG1478 treatment of cultures from asthmatic children had significant reductions in goblet cells at 0.2 μg/ml (p = 0.03) and 2 μg/ml (p = 0.003) as well as mucus secretion at 2 μg/ml (p = 0.04).

conclusionsWe have shown in this preliminary study that through EGF removal and tyrphostin AG1478 treatment the goblet cell number and mucus hypersecretion in differentiating air-liquid interface cultures from asthmatic children is significantly reduced. This further highlights the epidermal growth factor receptor as a potential therapeutic target to inhibit goblet cell hyperplasia and mucus hypersecretion in asthma.

Indexed as

AirModels, BiologicalAdolescentAsthmaBronchiCell CountCell DifferentiationCell ProliferationCells, CulturedChildChild, PreschoolElectric ImpedanceEpidermal Growth FactorFemaleGoblet CellsHumansEpidermal Growth FactorMucin 5ACQuinazolinesRNA, MessengerRTKI cpdTyrphostins

Identifiers

PMID26057128
PMCPMC4461195
OpenAlexW1537239195

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.