Evidence map›Paper›PMID 21193525›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2011

Gastrin stimulates expression of plasminogen activator inhibitor-1 in gastric epithelial cells.

Kristin G Nørsett, Islay Steele, Cedric Duval, Stephen J Sammut, Senthil V M Murugesan, Susan Kenny, Lucille Rainbow, Rod Dimaline, Graham J Dockray, D Mark Pritchard and 1 more

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
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  12. Novel roles of gastrin.The Journal of physiology · 2014
    Review
  13. Article
  14. Article
  15. The role of plasminogen activator inhibitor-1 in gastric mucosal protection.American journal of physiology. Gastrointestinal and liver physiology · 2013
    Article
  16. Article
  17. Article
  18. Gastrin receptor pharmacology.Current gastroenterology reports · 2012
    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

11 authors at 2 institutions in 1 country.

Kristin G NørsettPhysiological Laboratory, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Islay Steele
Cedric Duval
Stephen J Sammut
Senthil V M Murugesan
Susan Kenny
Lucille Rainbow
Rod Dimaline
Graham J Dockray
D Mark Pritchard
Andrea Varro
Physiological Society · GBUniversity of Liverpool · GB

Funding

Medical Research Council
6 · The paper itself

Abstract

Plasminogen activator inhibitor (PAI)-1 is associated with cancer progression, fibrosis and thrombosis. It is expressed in the stomach but the mechanisms controlling its expression there, and its biological role, are uncertain. We sought to define the role of gastrin in regulating PAI-1 expression and to determine the relevance for gastrin-stimulated cell migration and invasion. In gastric biopsies from subjects with elevated plasma gastrin, the abundances of PAI-1, urokinase plasminogen activator (uPA), and uPA receptor (uPAR) mRNAs measured by quantitative PCR were increased compared with subjects with plasma concentrations in the reference range. In patients with hypergastrinemia due to autoimmune chronic atrophic gastritis, there was increased abundance of PAI-1, uPA, and uPAR mRNAs that was reduced by octreotide or antrectomy. Immunohistochemistry revealed localization of PAI-1 to parietal cells and enterochromaffin-like cells in micronodular neuroendocrine tumors in hypergastrinemic subjects. Transcriptional mechanisms were studied by using a PAI-1-luciferase promoter-reporter construct transfected into AGS-G(R) cells. There was time- and concentration-dependent increase of PAI-1-luciferase expression in response to gastrin that was reversed by inhibitors of the PKC and MAPK pathways. In Boyden chamber assays, recombinant PAI-1 inhibited gastrin-stimulated AGS-G(R) cell migration and invasion, and small interfering RNA treatment increased responses to gastrin. We conclude that elevated plasma gastrin concentrations are associated with increased expression of gastric PAI-1, which may act to restrain gastrin-stimulated cell migration and invasion.

Indexed as

Enterochromaffin-like CellsEpithelial CellsGastrinsHumansOctreotidePlasminogen Activator Inhibitor 1Receptors, Urokinase Plasminogen ActivatorRNA, MessengerStomachUrokinase-Type Plasminogen ActivatorGastrinsOctreotidePlasminogen Activator Inhibitor 1Receptors, Urokinase Plasminogen ActivatorRNA, MessengerUrokinase-Type Plasminogen Activator

Identifiers

PMID21193525
PMCPMC3174540
OpenAlexW2049304586

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.