Evidence map›Paper›PMID 25843056›Full record

ArticleMolecular and cellular endocrinology2015

Selective inhibition of prostaglandin E2 receptors EP2 and EP4 modulates DNA methylation and histone modification machinery proteins in human endometriotic cells.

Joe A Arosh, JeHoon Lee, Anna Starzinski-Powitz, Sakhila K Banu

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular endocrinology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
7.6field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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  7. Review
  8. Changing prostaglandin E2 (PGEReproductive medicine and biology · 2022
    Article
  9. Article
  10. Peritoneal Modulators of EZH2-miR-155 Cross-Talk in Endometriosis.International journal of molecular sciences · 2021
    Article
  11. Review
  12. Article
  13. Article
  14. The Pathogenesis of Endometriosis: Molecular and Cell Biology Insights.International journal of molecular sciences · 2019
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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.

Joe A AroshReproductive Endocrinology and Cell Signaling Laboratory, Department of Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, 77843 Texas, USA. Electronic address: jarosh@cvm.tamu.edu.
JeHoon LeeReproductive Endocrinology and Cell Signaling Laboratory, Department of Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, 77843 Texas, USA.
Anna Starzinski-PowitzMolekulare Zellbiologie und Humangenetik, Institut für Zellbiologie und Neurowissenschaft, Siesmayerstraße 70, Geb. B, 60323 Frankfurt am Main, Germany.
Sakhila K BanuReproductive Endocrinology and Cell Signaling Laboratory, Department of Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, 77843 Texas, USA.
Texas A&M University · US

Funding

Role of miR15a and miR34c in PGE2 Signaling in the Pathogenesis of EndometriosisR01HD079625 · NICHD · TEXAS A&M AGRILIFE RESEARCH · PI AROSH, JOE A. · 2015 to 2019
$1.5M
Prostaglandin E2 Signaling in Growth and Pains of EndometriosisR21HD066248 · NICHD · TEXAS A&M UNIVERSITY · PI AROSH, JOE A. · 2011 to 2012
$403k
Molecular Basis of Treating Endometriosis by Prostaglandin E2 Receptor InhibitorsR21HD065138 · NICHD · TEXAS A&M UNIVERSITY · PI AROSH, JOE A. · 2011 to 2012
$395k
NICHD NIH HHS 1R21HD065138NICHD NIH HHS 1R21HD066248NICHD NIH HHS R01 HD079625NICHD NIH HHS R21 HD065138NICHD NIH HHS R21 HD066248
6 · The paper itself

Abstract

Endometriosis is an inflammatory gynecological disease of reproductive-age women. The prevalence of endometriosis is 5-10% in reproductive-age women. Modern medical treatments are directed to inhibit the action of estrogen in endometriotic cells. However, hormonal therapies targeting estrogen can be prescribed only for a short time because of their undesirable side effects. Recent studies from our laboratory, using human endometriotic epithelial cell line 12Z and stromal cell line 22B derived from red lesion, discovered that selective inhibition of prostaglandin E2 (PGE2) receptors EP2 and EP4 inhibits adhesion, invasion, growth, and survival of 12Z and 22B cells by modulating integrins, MMPs and TIMPs, cell cycle, survival, and intrinsic apoptotic pathways, suggesting multiple epigenetic mechanisms. The novel findings of the present study indicate that selective pharmacological inhibition of EP2 and EP4: (i) decreases expression of DNMT3a, DNMT3b, H3K9me3, H3K27me3, SUV39H1, HP1a, H3K27, EZH2, JMJD2a, HDAC1, HDAC3, MeCP2, CoREST and Sin3A; (ii) increases expression of H3K4me3, H3H9ac, H3K27ac; and (iii) does not modulate the expression of DNMT1, hSET1, LSD1, MBD1, p300, HDAC2, and JMJD3 epigenetic machinery proteins in an epithelial and stromal cell specific manner. In this study, we report for the first time that inhibition of PGE2-EP2/EP4 signaling modulates DNA methylation, H3 histone methylation and acetylation, and epigenetic memory machinery proteins in human endometriotic epithelial cells and stromal cells. Thus, targeting EP2 and EP4 receptors may emerge as long-term nonsteroidal therapy for treatment of active endometriotic lesions in women.

Indexed as

AcetylationBiphenyl CompoundsCell LineDNA MethylationEndometriosisEpigenesis, GeneticFemaleGene Expression RegulationHistonesHumansProstaglandin AntagonistsReceptors, Prostaglandin E, EP2 SubtypeReceptors, Prostaglandin E, EP4 SubtypeSignal TransductionXanthones6-isopropoxy-9-oxoxanthene-2-carboxylic acidAH 23848Biphenyl CompoundsHistonesProstaglandin AntagonistsPTGER2 protein, humanPTGER4 protein, humanReceptors, Prostaglandin E, EP2 SubtypeReceptors, Prostaglandin E, EP4 SubtypeXanthonesDNA methylationEndometriosisEP2 and EP4EpigeneticsHistone modificationPGE(2)

Identifiers

PMID25843056
PMCPMC6573013
OpenAlexW2039379432

What OpenQuestion holds

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LicenceTDM
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.