Evidence map›Paper›PMID 20228180›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2010

VEGF in the lung: a role for novel isoforms.

Julia Varet, Samantha K Douglas, Laura Gilmartin, Andrew R L Medford, David O Bates, Steven J Harper, Ann B Millar

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.2field-weighted citation impact, top 22% 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, 41 citations in OpenAlex.

  1. Review
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  8. Article
  9. The "Angiogenic Switch" and Functional Resources in Cyclic Sports Athletes.International journal of molecular sciences · 2021
    Review
  10. VEGFR1-tyrosine kinase signaling in pulmonary fibrosis.Inflammation and regeneration · 2021
    Review
  11. Review
  12. Endothelial Damage in Acute Respiratory Distress Syndrome.International journal of molecular sciences · 2020
    Review
  13. Review
  14. VEGF (Vascular Endothelial Growth Factor) and Fibrotic Lung Disease.International journal of molecular sciences · 2018
    Review
  15. Differential Expression of VEGF-AAmerican journal of respiratory and critical care medicine · 2017
    Article
  16. Article
  17. Article
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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

7 authors at 3 institutions in 1 country.

Julia VaretLung Research Group, Department of Clinical Science at North Bristol, University of Bristol Paul O'Gorman Lifeline Centre, Southmead Hospital, Westbury-on-Trym, United Kingdom.
Samantha K Douglas
Laura Gilmartin
Andrew R L Medford
David O Bates
Steven J Harper
Ann B Millar
Southmead Hospital · GBUniversity of Bristol · GBNorth Bristol NHS Trust · GB

Funding

British Heart Foundation BS/006/005Wellcome Trust 074702
6 · The paper itself

Abstract

Vascular endothelial cell growth factor (VEGF) is a potent mitogen and permogen that increases in the plasma and decreases in the alveolar space in respiratory diseases such as acute respiratory distress syndrome (ARDS). This observation has led to controversy over the role of this potent molecule in lung physiology and disease. We hypothesized that some of the VEGF previously detected in normal lung may be of the anti-angiogenic family (VEGF(xxx)b) with significant potential effects on VEGF bioactivity. VEGF(xxx)b protein expression was assessed by indirect immunohistochemistry in normal and ARDS tissue. Expression of VEGF(xxx)b was also detected by immunoblotting in normal lung tissue, primary human alveolar type II (ATII) cells, and bronchoalveolar lavage (BAL) fluid in normal subjects and by ELISA in normal, "at risk," and ARDS subjects. The effect of VEGF(165) and VEGF(165)b on both human primary endothelial cells and alveolar epithelial cell proliferation was assessed by [(3)H]thymidine uptake. We found that VEGF(165)b was widely expressed in normal healthy lung tissue but is reduced in ARDS lung. VEGF(121)b and VEGF(165)b were present in whole lung, BAL, and ATII lysate. The proliferative effect of VEGF(165) on both human primary endothelial cells and human alveolar epithelial cells was significantly inhibited by VEGF(165)b (P < 0.01). These data demonstrate that the novel VEGF(xxx)b family members are expressed in normal lung and are reduced in ARDS. A specific functional effect on primary human endothelial and alveolar epithelial cells has also been shown. These data suggest that the VEGF(xxx)b family may have a role in repair after lung injury.

Indexed as

AdolescentAdultAgedAged, 80 and overBronchoalveolar Lavage FluidCell ProliferationEndothelium, VascularFemaleHumansLungLung InjuryMaleMiddle AgedProtein IsoformsPulmonary AlveoliRespiratory Distress SyndromeProtein IsoformsVascular Endothelial Growth Factor AVascular Endothelial Growth FactorsVEGFA protein, human

Identifiers

PMID20228180
PMCPMC2886605
OpenAlexW2117399139

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.