Evidence map›Paper›PMID 19819266›Full record

ArticleBiochimica et biophysica acta2009

Prostaglandin F(2alpha)-F-prostanoid receptor regulates CXCL8 expression in endometrial adenocarcinoma cells via the calcium-calcineurin-NFAT pathway.

Kurt J Sales, David Maldonado-Pérez, Vivien Grant, Rob D Catalano, Martin R Wilson, Pamela Brown, Alistair R W Williams, Richard A Anderson, E Aubrey Thompson, Henry N Jabbour

Open access · hybridAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
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  10. Review
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  14. NFAT as cancer target: mission possible?Biochimica et biophysica acta · 2014
    Review
  15. Article
  16. Article
  17. NFAT gene family in inflammation and cancer.Current molecular medicine · 2013
    Review
  18. Article
  19. Article
  20. Lipopolysaccharide-induced cyclooxygenase-2 expression in mouse transformed Clara cells.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 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

10 authors at 3 institutions in 2 countries.

Kurt J SalesMRC Human Reproductive Sciences Unit, The Queen's Medical Research Institute, 47 Little France Crescent, The University of Edinburgh, Edinburgh, EH16 4TJ, UK.
David Maldonado-Pérez
Vivien Grant
Rob D Catalano
Martin R Wilson
Pamela Brown
Alistair R W Williams
Richard A Anderson
E Aubrey Thompson
Henry N Jabbour
The Queen's Medical Research Institute · GBUniversity of Edinburgh · GBMayo Clinic in Florida · US

Funding

Medical Research Council MC_U127684438Medical Research Council U.1276.00.004.00002.01
6 · The paper itself

Abstract

Pro-inflammatory mediators, like prostaglandin (PG) and chemokines, promote tumourigenesis by enhancing cell proliferation, migration of immune cells and recruitment of blood vessels. Recently we showed elevated expression of the chemokine (C-X-C motif) receptor 2 (CXCR2) in endometrial adenocarcinomas localized to neutrophils and neoplastic epithelial and vascular cells. Furthermore we found that PGF(2alpha)-F-prostanoid (FP) receptor regulates the expression of the CXCR2 ligand CXCL1, to promote neutrophil chemotaxis in endometrial adenocarcinomas. In the present study we identified another CXCR2 ligand, CXCL8 as a target for PGF(2alpha)-FP receptor signalling which enhances epithelial cell proliferation in endometrial adenocarcinoma cells in vitro and in nude mice in vivo. We found that PGF(2alpha)-FP receptor interaction induces CXCL8 expression in endometrial adenocarcinoma cells via the protein kinase C-calcium-calcineurin-NFAT signaling pathway. Promoter analysis revealed that CXCL8 transcriptional activation by PGF(2alpha) signaling is mediated by cooperative interactions between the AP1 and NFAT binding sites. Furthermore, PGF(2alpha) via the FP receptor induced the expression of the regulator of calcineurin 1 isoform 4 (RCAN1-4) via the calcineurin/NFAT pathway in a reciprocal manner to CXCL8. Using an adenovirus to overexpress RCAN1-4, we found that RCAN1-4 is a negative regulator of CXCL8 expression in endometrial adenocarcinoma cells. Taken together our data have elucidated the molecular and cellular mechanism whereby PGF(2alpha) regulates CXCL8 expression via the FP receptor in endometrial adenocarcinomas and have highlighted RCAN1-4 as a negative regulator of CXCL8 expression which may be exploited therapeutically to inhibit CXCL8-mediated tumour development.

Indexed as

Gene Expression Regulation, NeoplasticSignal TransductionAdenocarcinomaAnimalsCalcineurinCalciumCell Line, TumorDinoprostEndometrial NeoplasmsFemaleHumansInterleukin-8MiceMice, NudeNeoplasm ProteinsNeoplasm TransplantationCalcineurinCalciumCXCL8 protein, humanDinoprostInterleukin-8Neoplasm ProteinsNFATC Transcription Factorsprostaglandin F2alpha receptorProtein Kinase CReceptors, Prostaglandin

Identifiers

PMID19819266
PMCPMC2806519
OpenAlexW2164028133

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.