Evidence map›Paper›PMID 41187054›Full record

ArticleReproduction & fertility2025

Canine endometrial organoids respond to exogenous steroid hormones and are an in vitro model for cystic endometrial hyperplasia.

Riley E Thompson, Alexandria M Horner, Charissa Ehresman, Ahmed Gad, Mindy A Meyers, Jennifer Palmer, Dn Rao Veeramachaneni, Budhan S Pukazhenthi, Fiona K Hollinshead

Abstract read
In one paragraph

Article in Reproduction & fertility, 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

9 authors.

Riley E ThompsonDepartment of Clinical Sciences, Colorado State University, Fort Collins, Colorado, USA.ORCID 0000-0003-1592-1307
Alexandria M HornerDepartment of Clinical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Charissa EhresmanDepartment of Clinical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Ahmed GadDepartment of Clinical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Mindy A MeyersDepartment of Clinical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Jennifer PalmerAnimal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins, Colorado, USA.
Dn Rao VeeramachaneniAnimal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins, Colorado, USA.
Budhan S PukazhenthiCenter for Species Survival, Smithsonian's National Zoo and Conservation Biology Institute, Front Royal, Virginia, USA.
Fiona K HollinsheadDepartment of Clinical Sciences, Colorado State University, Fort Collins, Colorado, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abstract: The etiology, epidemiology, and pathogenesis of many uterine diseases, including endometritis, cystic endometrial hyperplasia (CEH), and pyometra, remain poorly understood in canids, hindering the advancement of effective preventative therapeutics to ultimately improve fertility. The development of an in vitro endometrial cell culture system that mimics in vivo architecture, cellular morphology, and physiological responses would facilitate a greater understanding of the mechanisms of complex canine uterine diseases and reduce the need for in vivo research. Three-dimensional organoid cell cultures may provide an innovative approach for studying uterine pathologies in the bitch. Unlike traditional two-dimensional monolayer cell culture systems, organoids can be grown long-term while maintaining the structure, phenotype, and function of their organ of origin. Here, we report the generation and characterization of canine endometrial organoids via immunohistochemistry (IHC), transmission electron microscopy, and RT-qPCR, and demonstrate their responsiveness to exogenous steroid hormones mimicking the estrous cycle. Furthermore, gene expression of key inflammatory markers was upregulated in endometrial organoids derived from bitches with CEH compared to organoids derived from healthy tissue. Findings highlight canine endometrial organoids as a valuable model to study both normal uterine physiology and disease-related processes in dogs. Lay summary: Organoids are cells that are grown three-dimensionally in the laboratory and retain similar functions to the organ from which the cells were collected. Organoids were used here to study female dog reproductive tissue without the need for live animals, which saves time and money and improves animal welfare. We developed a three-dimensional model of the dog uterus that responds to reproductive hormones and maintains its normal structure. In addition, we used diseased canine tissue to replicate CEH, a condition that affects pregnancy and can lead to the serious disease of pyometra, in which the uterus is infected and filled with pus. In future studies, this validated model can be used to study how CEH develops and to test new treatments for the disease.

Indexed as

Dog DiseasesEndometrial HyperplasiaEndometriumOrganoidsAnimalsDisease Models, AnimalDogsFemale3D culturebitchcaninedogendometriumestrogenorganoidprogesteronepyometrauterus

Identifiers

PMID41187054
PMCPMC12623135

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.