Evidence map›Paper›PMID 31814282›Full record

Trial reportJournal of cellular and molecular medicine2020

A new trick for an old dog: The application of mifepristone in the treatment of adenomyosis.

Xuan Che, Jianzhang Wang, Jiayi He, Qin Yu, Wenting Sun, Shuyi Chen, Gen Zou, Tiantian Li, Xinyue Guo, Xinmei Zhang

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Signaling pathways and advances in targeted therapy for adenomyosis.Frontiers in cell and developmental biology · 2025
    Review
  9. Review
  10. Review
  11. Review
  12. Article
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  14. Review
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

10 authors at 2 institutions in 1 country.

Xuan CheWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Jianzhang WangWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Jiayi HeWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Qin YuWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Wenting SunWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Shuyi ChenWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Gen ZouWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Tiantian LiWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Xinyue GuoWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Xinmei ZhangWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.ORCID 0000-0001-6474-3477
Women's Hospital, School of Medicine, Zhejiang University · CNJiaxing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adenomyosis is also called internal endometriosis and affects about 20% of reproductive-aged women. It seriously reduces life quality of patients because current drug therapies face with numerous challenges. Long-term clinical application of mifepristone exhibits wonderful therapeutic effects with mild side-effects in many disorders since 1982. Since adenomyosis is a refractory disease, we investigate whether mifepristone can be applied in the treatment of adenomyosis. In this study, we investigated the direct effects of mifepristone on human primary eutopic endometrial epithelial cells and stromal cells in adenomyosis. We found that mifepristone causes cell cycle arrest through inhibiting CDK1 and CDK2 expressions and induces cell apoptosis via the mitochondria-dependent signalling pathway in endometrial epithelial cells and stromal cells of adenomyosis. Furthermore, mifepristone inhibits the migration of endometrial epithelial cells and stromal cells through decreasing CXCR4 expression and restricts the invasion of endometrial epithelial cells via suppression of epithelial-mesenchymal transition in adenomyosis. We also found that mifepristone treatment decreases the uterine volume, CA125 concentration and increases the haemoglobin concentration in serum for adenomyosis patients. Therefore, we demonstrate that mifepristone could serve as a novel therapeutic drug in the treatment of adenomyosis, and therefore, the old dog can do a new trick.

Indexed as

AdenomyosisApoptosisCell Cycle CheckpointsCell MovementCell SurvivalEndometriumEpithelial CellsEpithelial-Mesenchymal TransitionFemaleGene Expression RegulationHumansMifepristoneMitochondriaModels, BiologicalReceptors, CXCR4Signal TransductionCXCR4 protein, humanMifepristoneReceptors, CXCR4adenomyosisapoptosisinvasionmifepristonemigrationproliferation

Identifiers

PMID31814282
PMCPMC6991631
OpenAlexW2993077669

What OpenQuestion holds

Textmetadata
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.