Evidence map›Paper›PMID 41760717›Full record

ArticleScientific reports2026

Establishment of a xenograft model of endometriosis-associated fibrosis using human immortalized endometrial stromal cells overexpressing HOXC8.

Hitomi Takasaki-Kawasaki, Shun Sato, Tetsuro Tamehisa, Toshihide Yoneda, Amon Shiroshita, Taishi Fujimura, Isao Tamura, Ryo Maekawa, Norihiro Sugino

Abstract read
In one paragraph

Article in Scientific reports, 2026. 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.

Hitomi Takasaki-KawasakiDepartment of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Japan.
Shun SatoDepartment of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Japan.
Tetsuro TamehisaDepartment of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Japan.
Toshihide YonedaDepartment of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Japan.
Amon ShiroshitaDepartment of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Japan.
Taishi FujimuraDepartment of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Japan.
Isao TamuraDepartment of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Japan.
Ryo MaekawaDepartment of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Japan.
Norihiro SuginoDepartment of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Japan. sugino@yamaguchi-u.ac.jp.

Funding

Japan Society for the Promotion of Science 23K27734Japan Society for the Promotion of Science 24K12533Japan Society for the Promotion of Science 24K12579Japan Society for the Promotion of Science 25K20119
6 · The paper itself

Abstract

Endometriosis is a disease characterized by fibrosis and adhesions. There are still no treatment methods targeting these conditions. One reason for this is the lack of useful animal models to investigate the mechanisms of fibrosis and adhesion in endometriosis. We previously proposed that Homeobox C8 (HOXC8) acts as an upstream regulator involved in endometriosis development, promoting fibrosis by activating transforming growth factor β (TGFB) signaling in vitro. This study was undertaken to establish a xenograft mouse model for endometriosis-associated fibrosis using HOXC8-overexpressing cells. Stable lines of immortalized human endometrial stromal cells overexpressing HOXC8 (HOXC8-imESCs) and mock control lines (Control-imESCs) were established and evaluated for cellular functions in vitro. These cell lines were then transplanted under the renal capsule of severely immunodeficient mice, and the xenografts were harvested five weeks after transplantation. In vitro, cell migration, invasion, and fibrotic capacity were enhanced in HOXC8-imESCs compared to Control-imESCs. In the xenografts, HOXC8-imESCs exhibited significant collagen fiber production compared to Control-imESCs. Additionally, immunohistochemistry of the xenografts detected phosphorylated SMAD2/3 exclusively in HOXC8-imESCs, indicating that HOXC8 overexpression activates the TGFB/SMAD pathway aberrantly in vivo. In this study, a new animal model for endometriosis-associated fibrosis was established using the HOXC8-imESC xenograft model system.

Indexed as

Disease Models, AnimalEndometriosisHomeodomain ProteinsAnimalsCell LineHeterograftsHumansMiceMice, SCIDSignal TransductionHomeodomain ProteinsHOXC8 protein, humanEndometrial stromal cellsEndometriosisFibrosisHOXC8TGFB/SMAD pathwayXenograft model

Identifiers

PMID41760717
PMCPMC13049066

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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.