Evidence map›Paper›PMID 18245266›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2008

Hepatocyte growth factor regulates cyclooxygenase-2 expression via beta-catenin, Akt, and p42/p44 MAPK in human bronchial epithelial cells.

Young H Lee, Yuichiro J Suzuki, Autumn J Griffin, Regina M Day

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2008. 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
2.2field-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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
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  9. Article
  10. Co-targeting c-Met and COX-2 leads to enhanced inhibition of lung tumorigenesis in a murine model with heightened airway HGF.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2014
    Article
  11. Article
  12. Article
  13. Review
  14. A tandem repeat of a fragment of Listeria monocytogenes internalin B protein induces cell survival and proliferation.American journal of physiology. Lung cellular and molecular physiology · 2010
    Article
  15. Article
  16. Article
  17. Article
  18. Epithelial repair mechanisms in the lung.American journal of physiology. Lung cellular and molecular physiology · 2010
    Review
  19. Article
  20. TNF-induced activation of pulmonary microvessel endothelial cells: a role for GSK3beta.American journal of physiology. Lung cellular and molecular physiology · 2009
    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

4 authors at 1 institution in 1 country.

Young H LeeDepartment of Pharmacology, The Uniformed Services University of the Health Sciences, Bethesda, MD 20814-4799, USA.
Yuichiro J Suzuki
Autumn J Griffin
Regina M Day
Uniformed Services University of the Health Sciences · US

Funding

Mechanism of apoptosis in lung vascular smooth muscleR01HL072844 · NHLBI · TUFTS UNIVERSITY BOSTON · PI SUZUKI, YUICHIRO JUSTIN · 2003 to 2017
$3.3M
HGF Signaling in Pulmonary RemodelingR01HL073929 · NHLBI · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI DAY, REGINA M · 2004 to 2007
$1.0M
Signaling for cardioprotection against oxidative stressR01HL067340 · NHLBI · TUFTS UNIVERSITY BOSTON · PI SUZUKI, YUICHIRO JUSTIN · 2003 to 2006
$931k
NHLBI NIH HHS R01 HL067340NHLBI NIH HHS R01-HL-067340NHLBI NIH HHS R01 HL072844NHLBI NIH HHS R01-HL-072844NHLBI NIH HHS R01 HL073929NHLBI NIH HHS R01-HL-073929
6 · The paper itself

Abstract

Hepatocyte growth factor (HGF) is upregulated in response to lung injury and has been implicated in tissue repair through its antiapoptotic and proliferative activities. Cyclooxygenase-2 (COX-2) is an inducible enzyme in the biosynthetic pathway of prostaglandins, and its activation has been shown to play a role in cell growth. Here, we report that HGF induces gene transcription of COX-2 in human bronchial epithelial cells (HBEpC). Treatment of HBEpC with HGF resulted in phosphorylation of the HGF receptor (c-Met), activation of Akt, and upregulation of COX-2 mRNA. Adenovirus-mediated gene transfer of a dominant negative (DN) Akt mutant revealed that HGF increased COX-2 mRNA in an Akt-dependent manner. COX-2 promoter analysis in luciferase reporter constructs showed that HGF regulation required the beta-catenin-responsive T cell factor-4 binding element (TBE). The HGF activation of the COX-2 gene transcription was blocked by DN mutant of beta-catenin or by inhibitors that blocked activation of Akt. Inhibition of p42/p44 MAPK pathway blocked HGF-mediated activation of beta-catenin gene transcription but not Akt activation, suggesting that p42/p44 MAPK acts in a parallel mechanism for beta-catenin activation. We also found that inhibition of COX-2 with NS-398 blocked HGF-induced growth in HBEpC. Together, the results show that the HGF increases COX-2 gene expression via an Akt-, MAPK-, and beta-catenin-dependent pathway in HBEpC.

Indexed as

Adenoviruses, Humanbeta CateninBronchiCells, CulturedCyclooxygenase 2Gene Transfer TechniquesHepatocyte Growth FactorHumansMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Oligonucleotide Array Sequence AnalysisPromoter Regions, GeneticProto-Oncogene Proteins c-aktRNA, Messengerbeta CateninCyclooxygenase 2Hepatocyte Growth FactorMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Proto-Oncogene Proteins c-aktRNA, Messenger

Identifiers

PMID18245266
PMCPMC2427436
OpenAlexW2129738723

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.