Evidence map›Paper›PMID 40683665›Full record

ArticleJournal of the American Association for Laboratory Animal Science : JAALAS2025

Induction of Endometriosis in a Menstruating Mouse Model (Mus musculus): A Translational Animal Disease Model.

Christina A Howe, John J Coté, Catherine T Stoos, Jodi J Hallgren, Marley R Bredehoeft, Janee B Gelineau-van Waes

Abstract read
In one paragraph

Article in Journal of the American Association for Laboratory Animal Science : JAALAS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Christina A Howe1Research Compliance, Creighton University School of Medicine, Omaha, Nebraska.
John J Coté2Department of Obstetrics and Gynecology, CHI Health, Creighton University Medical Center, Omaha, Nebraska.
Catherine T Stoos3CHI Health, Creighton University Medical Center and Methodist Pathology Center, Methodist Hospital, Omaha, Nebraska; and.
Jodi J Hallgren4Department of Pharmacology and Neuroscience, Creighton University School of Medicine, Omaha, Nebraska.
Marley R Bredehoeft4Department of Pharmacology and Neuroscience, Creighton University School of Medicine, Omaha, Nebraska.
Janee B Gelineau-van Waes4Department of Pharmacology and Neuroscience, Creighton University School of Medicine, Omaha, Nebraska.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Improved animal models of endometriosis are needed to accurately represent the pathophysiology of human disease and identify new therapeutic targets that do not compromise fertility. There is tremendous heterogeneity among published rodent models of endometriosis, and the etiology and pathogenesis of endometriosis remain undetermined. The vast majority of endometriosis is found in menstruating women; however, no published mouse models have induced endometriosis in a menstruating mouse, further limiting our understanding of the disease. Our goal was to develop a novel, translationally relevant mouse model of endometriosis in a menstruating mouse by transplanting donor menstrual endometrium into the peritoneal cavity of menstruating, immunocompetent, intact recipients. We initially compared 4 different experimental groups to optimize implanted menstrual tissue type and method of implantation into intact, normally cycling recipient mice. To further optimize this model, a novel fifth experimental group was compared in which discrete pieces of menstrual donor endometrium were implanted via laparoscopy into menstruating recipient mice. Lesions were confirmed to be endometriosis based on histopathology. The use of laparoscopy to place discrete fragments of menstrual phase endometrium intraabdominally was the most effective method for induction of endometriosis. This method was just as effective when used to induce endometriosis in menstruating recipient mice. Menstruating mice returned to normal estrus cyclicity after induction of disease, which can allow for assessment of therapeutic interventions on fertility. This is a novel translationally relevant mouse model of endometriosis in a menstruating mouse that can be used to explore and elucidate the etiology and pathogenesis of this disease.

Indexed as

B6, B6(Cg)-Tyrc-2J/JmCherry, B6(Cg)-Tyrc-2JTg(UBC-mCherry)1Phbs/J

Identifiers

PMID40683665
PMCPMC12379715

What OpenQuestion holds

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Registered trials

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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.