Evidence map›Paper›PMID 22838404›Full record

ArticleRespiratory research2012

WNT7B in fibroblastic foci of idiopathic pulmonary fibrosis.

Travis Meuten, Ariel Hickey, Katherine Franklin, Brian Grossi, Jeremy Tobias, Donna R Newman, Samuel H Jennings, Maria Correa, Philip L Sannes

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
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  14. Clinical and molecular features of rapidly progressive chronic hypersensitivity pneumonitis.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2017
    Article
  15. Distinct Roles of Wnt/Mediators of inflammation · 2017
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Expression of WNT5A in Idiopathic Pulmonary Fibrosis and Its Control by TGF-β and WNT7B in Human Lung Fibroblasts.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 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

9 authors at 1 institution in 1 country.

Travis MeutenDepartments of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607, USA.
Ariel Hickey
Katherine Franklin
Brian Grossi
Jeremy Tobias
Donna R Newman
Samuel H Jennings
Maria Correa
Philip L Sannes
North Carolina State University · US

Funding

ALVEOLAR BASEMENT MEMBRANE/CELL INTERACTIONS IN THE LUNGR01HL044497 · NHLBI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI SANNES, PHILIP L. · 1992 to 2013
$3.7M
Alveolar Basement Membrane/Cell Interactions in the LungR56HL044497 · NHLBI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI SANNES, PHILIP L. · 2008 to 2008
$371k
Differentiation of Alveolar Epithelium in Pulmonary FibrosisR03HL095411 · NHLBI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI SANNES, PHILIP L. · 2009 to 2010
$149k
NHLBI NIH HHS HL44497NHLBI NIH HHS HL95411NHLBI NIH HHS R01 HL044497
6 · The paper itself

Abstract

backgroundIdiopathic pulmonary fibrosis (IPF) is a devastating interstitial pneumonia causing a loss of respiratory surface area due to a proliferative fibrotic response involving hyperplastic, hypertrophic, and metaplastic epithelium, cystic honeycomb change, septal expansion, and variable inflammation. Wnt (wingless) signaling glycoproteins are known to be involved in lung development and tissue repair, and are up-regulated in patients with IPF. Based on previous qRT-PCR data showing increased Wnt7B in lungs of IPF patients, a systematic, quantitative examination of its tissue site distribution was undertaken.

methodsTissue samples from the Lung Tissue Research Consortium (LTRC) of 39 patients diagnosed with mild to severe IPF/usual interstitial pneumonia (UIP) and 19 normal patients were examined for the immunolocalization of Wnt7B.

resultsIn normal lung, moderate Wnt7B reactivity was confined to airway epithelium, smooth muscle of airways and vasculature, and macrophages. IPF lung showed strong Wnt7B reactivity in fibroblastic foci, dysplastic airway and alveolar epithelium, and in highly discrete subepithelial, basement membrane-associated regions. All reactive sites were sized and counted relative to specific microscopic regions. Those in the subepithelial sites were found in significantly greater numbers and larger relative area compared with the others. No reactive sites were present in normal patient controls.

conclusionsThe results demonstrate Wnt7B to be expressed at high concentrations in regions of active hyperplasia, metaplasia, and fibrotic change in IPF patients. In this context and its previously established biologic activities, Wnt7B would be expected to be of potential importance in the pathogenesis of IPF.

Indexed as

AgedAged, 80 and overBasement MembraneFemaleFibroblastsHumansIdiopathic Pulmonary FibrosisMacrophagesMaleMiddle AgedMuscle, SmoothRespiratory MucosaRespiratory SystemSeverity of Illness IndexWnt ProteinsWNT7B protein, humanWnt Proteins

Identifiers

PMID22838404
PMCPMC3479038
OpenAlexW2098459324

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.