Evidence map›Paper›PMID 28548231›Full record

ArticleBritish journal of pharmacology2017

Combination therapy with telmisartan and parecoxib induces regression of endometriotic lesions.

Anca Nenicu, Yuan Gu, Christina Körbel, Michael D Menger, Matthias W Laschke

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Catamenial Pneumothorax-Still an Unveiled Disease.Medicina (Kaunas, Lithuania) · 2024
    Review
  3. Review
  4. Review
  5. Article
  6. Endometriosis and cardiovascular disease.European heart journal open · 2022
    Article
  7. Article
  8. Review
  9. Review
  10. Cyclooxygenase-2 in Endometriosis.International journal of biological sciences · 2019
    Review
  11. 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

5 authors at 1 institution in 1 country.

Anca NenicuInstitute for Clinical & Experimental Surgery, Saarland University, Homburg/Saar, Germany.
Yuan GuInstitute for Clinical & Experimental Surgery, Saarland University, Homburg/Saar, Germany.
Christina KörbelInstitute for Clinical & Experimental Surgery, Saarland University, Homburg/Saar, Germany.
Michael D MengerInstitute for Clinical & Experimental Surgery, Saarland University, Homburg/Saar, Germany.
Matthias W LaschkeInstitute for Clinical & Experimental Surgery, Saarland University, Homburg/Saar, Germany.ORCID http://orcid.org/0000-0002-7847-8456
Saarland University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeTelmisartan suppresses the development of endometriotic lesions. However, the drug also up-regulates the expression of COX-2, which has been suggested to promote the progression of endometriosis. Accordingly, in the present study we analysed whether a combination therapy with telmisartan and a COX-2 inhibitor may be more effective in the treatment of endometriotic lesions than the application of telmisartan alone. EXPERIMENTAL APPROACH: Endometriotic lesions were induced in the peritoneal cavity of C57BL/6 mice, which were treated daily with an i.p. injection of telmisartan (10 mg·kg KEY

resultsTelmisartan-treated lesions exhibited a significantly reduced lesion volume when compared with vehicle-treated controls and parecoxib-treated lesions. This inhibitory effect of telmisartan was even more pronounced when it was used in combination with parecoxib. The combination therapy resulted in a reduced microvessel density as well as lower numbers of proliferating Ki67-positive cells and higher numbers of apoptotic cleaved caspase-3-positive stromal cells within the lesions. This was associated with a lower expression of COX-2, MMP-9 and p-Akt/Akt when compared with controls. The application of the two drugs further inhibited the ingrowth of nerve fibres into the lesions. CONCLUSIONS AND IMPLICATIONS: Combination therapy with telmisartan and a COX-2 inhibitor represents a novel, effective pharmacological strategy for the treatment of endometriosis.

Indexed as

Angiotensin II Type 1 Receptor BlockersAnimalsBenzimidazolesBenzoatesCaspase 3Cyclooxygenase 2Cyclooxygenase 2 InhibitorsDisease Models, AnimalDrug Therapy, CombinationEndometriosisFemaleIsoxazolesMatrix Metalloproteinase 9Mice, Inbred C57BLPPAR gammaProto-Oncogene Proteins c-aktAngiotensin II Type 1 Receptor BlockersBenzimidazolesBenzoatesCasp3 protein, mouseCaspase 3Cyclooxygenase 2Cyclooxygenase 2 InhibitorsIsoxazolesMatrix Metalloproteinase 9Mmp9 protein, mouseparecoxibPPAR gammaProto-Oncogene Proteins c-aktPtgs2 protein, mouseTelmisartan

Identifiers

PMID28548231
PMCPMC5522992
OpenAlexW2619259607

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.