Evidence map›Paper›PMID 23463699›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Regulation of Wnt4 in chronic obstructive pulmonary disease.

Andrew L Durham, Alistair McLaren, Brian P Hayes, Gaetano Caramori, Chris L Clayton, Peter J Barnes, K Fan Chung, Ian M Adcock

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Exploring the Roles of Wnt Signaling Pathway and Non-Coding RNAs in COPD.International journal of chronic obstructive pulmonary disease · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. WNT Signalling in Lung Physiology and Pathology.Handbook of experimental pharmacology · 2021
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. BET-ting on Nrf2: How Nrf2 Signaling can Influence the Therapeutic Activities of BET Protein Inhibitors.BioEssays : news and reviews in molecular, cellular and developmental biology · 2018
    Review
  14. Thorax · 2017
    Review
  15. Article
  16. Article
  17. WNT/β-catenin signaling regulates cigarette smoke-induced airway inflammation via the PPARδ/p38 pathway.Laboratory investigation; a journal of technical methods and pathology · 2016
    Article
  18. Non-canonical WNT signalling in the lung.Journal of biochemistry · 2015
    Review
  19. Article
  20. Integrative genomics of chronic obstructive pulmonary disease.Biochemical and biophysical research communications · 2014
    Review
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 4 institutions in 3 countries.

Andrew L DurhamAirways Disease Section, National Heart and Lung Institute, Imperial College London, London, UK. a.durham@imperial.ac.uk
Alistair McLaren
Brian P Hayes
Gaetano Caramori
Chris L Clayton
Peter J Barnes
K Fan Chung
Ian M Adcock
GlaxoSmithKline (United Kingdom) · GBImperial College London · GBLung Institute · USUniversity of Ferrara · IT

Funding

Medical Research CouncilWellcome Trust
6 · The paper itself

Abstract

Chronic obstructive pulmonary disease (COPD) is associated with persistent inflammation and oxidative stress in susceptible individuals. Using microarray analysis of bronchial biopsy samples from patients with COPD and controls, we identified Wnt4 as being up-regulated in COPD. Analysis of bronchial biopsy samples showed a very strong correlation between Wnt4 and IL8 gene expression, suggesting that Wnt4 plays a role in chronic lung inflammation. In vitro, Wnt4 induced proliferation and inflammation in human epithelial cells (BEAS-2B) and normal primary human bronchial epithelial cells in a concentration-dependent manner. This effect was enhanced in the presence of interleukin-1β (IL-1β) as a result of activation of the p38 and c-Jun NH2-terminal kinase mitogen-activated protein kinase pathways. Hydrogen peroxide, but not proinflammatory stimuli, up-regulated Wnt4 expression in epithelial cells. In monocytic THP-1 and primary airway smooth muscle cells, Wnt4 induced inflammation and enhanced the inflammatory response to lipopolysaccharide and IL-1β but did not induce proliferation. In addition, these other cell types did not have enhanced Wnt4 expression in response to hydrogen peroxide. Our results indicate that airway epithelial activation, due to oxidative stress, may lead to Wnt4 induction. Wnt4, in turn, acts through the noncanonical pathway to activate epithelial cell remodeling and IL8 gene expression, leading to neutrophil infiltration and inflammation.

Indexed as

AdultAgedAnimalsBronchiCase-Control StudiesCell LineCells, CulturedDisease Models, AnimalFemaleHumansInflammation MediatorsInterleukin-8MaleMiceMice, Inbred C57BLMiddle AgedInflammation MediatorsInterleukin-8Wnt4 ProteinWNT4 protein, humanepithelial cellsinflammationproliferation

Identifiers

PMID23463699
PMCPMC3659349
OpenAlexW2123994850

What OpenQuestion holds

Textmetadata
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.