Evidence map›Paper›PMID 40628400›Full record

SynthesisMolecular human reproduction2025

WERF Endometriosis Phenome and Biobanking Harmonisation Project for Experimental Models in Endometriosis Research (EPHect-EM-Homologous): homologous rodent models.

Katherine A Burns, Daniëlle Peterse, Caroline B Appleyard, Ronald Chandler, Sun-Wei Guo, Amelia Pearson, Eleonora Persoons, Michael S Anglesio, Michael S Rogers, Kathy L Sharpe-Timms and 9 more

Erratum issuedAbstract readSystematic Review
In one paragraph

Synthesis in Molecular human reproduction, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Identification of potent inhibitors of JUN N-terminal kinases for treatment of endometriosis and associated pain.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Katherine A BurnsDepartment of Environmental and Public Health Sciences, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Daniëlle PeterseDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Caroline B AppleyardDepartment of Basic Sciences, Ponce Health Sciences University-Ponce Research Institute, Ponce, PR, USA.
Ronald ChandlerDepartment of Obstetrics, Gynecology and Reproductive Biology, College of Human Medicine, Michigan State University, Grand Rapids, MI, USA.ORCID 0000-0001-5775-2594
Sun-Wei GuoResearch Institute, Shanghai Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.ORCID 0000-0002-8511-7624
Amelia PearsonDepartment of Environmental and Public Health Sciences, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Eleonora PersoonsDepartment of Development and Regeneration, University of Leuven, Leuven, Belgium.ORCID 0000-0003-1685-9963
Michael S AnglesioDepartment of Obstetrics and Gynaecology, University of British Columbia, Vancouver, BC, Canada.
Michael S RogersDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Kathy L Sharpe-TimmsDepartment of Obstetrics, Gynecology and Women's Health, The University of Missouri School of Medicine, Columbia, MO, USA.
Joris VriensDepartment of Development and Regeneration, University of Leuven, Leuven, Belgium.ORCID 0000-0002-2502-0409
Stacey L McAllisterDepartment of Gynecology and Obstetrics, Emory School of Medicine, Atlanta, GA, USA.
Kelsi N DoddsCollege of Medicine and Public Health and Flinders Health and Medical Research Institute, Flinders University, Bedford Park, SA, Australia.
Fiona L CousinsThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia.
Lone HummelshojWorld Endometriosis Research Foundation, London, UK.
Stacey A MissmerWorld Endometriosis Research Foundation, London, UK.
Kaylon L Bruner-TranWorld Endometriosis Research Foundation, London, UK.
Erin GreavesWorld Endometriosis Research Foundation, London, UK.ORCID 0000-0001-9165-5851
EPHect Experimental Models Working Group

Funding

The Role of the Matrisome in Endometriosis DevelopmentR01HD097597 · NICHD · UNIVERSITY OF CINCINNATI · PI BURNS, KATHERINE ANNE · 2019 to 2023
$2.2M
NICHD NIH HHS R01 HD097597NIH HHS R01 HD097597World Endometriosis Research Foundation
6 · The paper itself

Abstract

In vivo models of endometriosis enable the discovery and preclinical testing of new therapies. Several rodent models of endometriosis exist, but a lack of harmonization impedes reproducibility and comparability of results among investigators. Homologous models are advantageous as they allow the contribution of the immune system/inflammation to be studied. We reviewed published homologous rodent models of endometriosis to develop standard operating procedures ('EPHect-EM-Homologous-SOPs') to guide and facilitate the choice and implementation of these models and harmonize documentation to enhance interpretation and comparability of results. The World Endometriosis Research Foundation (WERF) established an international working group of experts in models of endometriosis and formed a working sub-group to discuss homologous rodent models of endometriosis. A systematic literature review and detailed analysis of protocols was performed. The identified models have advantages and limitations regarding physiological relevance and utility. To harmonize key variables for endometriosis rodent models, the working group focused on species and animal strains, placement of ectopic tissue, uterine tissue volume, method of induction, hormonal status, and uterine tissue 'type'. A decision tree and recommendations on model use were developed for mice and rats to serve as guides for the use of harmonized EPHect-EM-Homologous-SOPs, experimental design, reporting standards, and research of question-dependent key variables. No 'ideal' homologous model of endometriosis was identified. The choice of model for specific research should be guided according to a best-fit strategy. Harmonization of SOPs, documentation, and reporting standards will improve replicability and translational applicability of studies and better highlight where de novo model creation is needed.

Indexed as

Biological Specimen BanksDisease Models, AnimalEndometriosisAnimalsFemaleHumansMiceRatscollaborationendometriosisexperimental modelshomologousresearchrodents

Identifiers

PMID40628400
PMCPMC12237519

What OpenQuestion holds

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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.