Evidence map›Paper›PMID 35052864›Full record

ArticleBiomedicines2022

Ribosome Biogenesis Serves as a Therapeutic Target for Treating Endometriosis and the Associated Complications.

Cherry Yin-Yi Chang, An-Jen Chiang, Man-Ju Yan, Ming-Tsung Lai, Yun-Yi Su, Hsin-Yi Huang, Chan-Yu Chang, Ya-Hui Li, Pei-Fen Li, Chih-Mei Chen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Endometriosis: An Immunologist's Perspective.International journal of molecular sciences · 2025
    Review
  4. Review
  5. Article
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

14 authors at 8 institutions in 2 countries.

Cherry Yin-Yi ChangDepartment of Obstetrics and Gynecology, China Medical University Hospital, Taichung 404332, Taiwan.
An-Jen ChiangDepartment of Obstetrics and Gynecology, Kaohsiung Veterans General Hospital, Kaohsiung 813414, Taiwan.
Man-Ju YanInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
Ming-Tsung LaiDepartment of Pathology, Taichung Hospital, Ministry of Health and Welfare, Taichung 403301, Taiwan.
Yun-Yi SuInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
Hsin-Yi HuangInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
Chan-Yu ChangInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
Ya-Hui LiInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
Pei-Fen LiInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
Chih-Mei ChenHuman Genetic Center, China Medical University Hospital, Taichung 404332, Taiwan.
Tritium HwangInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
Chloe HoggMedical Research Council Centre for Reproductive Health, The University of Edinburgh, Edinburgh EH16 4TJ, UK.
Erin GreavesCentre for Early Life, Warwick Medical School, University of Warwick, Coventry CV4 7AL, UK.
Jim Jinn-Chyuan SheuInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
National Sun Yat-sen University · TWChina Medical University · TWChina Medical University Hospital · TWKaohsiung Medical University · TWKaohsiung Veterans General Hospital · TWMinistry of Health and Welfare · TWUniversity of Edinburgh · GBUniversity of Warwick · GB

Funding

China Medical University Hospital DMR108-078Medical Research Council M.R./M009238/1Medical Research Council M.R./S002456/2Medical Research Council MR/S002456/2Ministry of Science and Technology, Taiwan 107 -2911-I-110 -505Ministry of Science and Technology, Taiwan 107 -2912-I-110 -510Ministry of Science and Technology, Taiwan 108-2911-I-110-501Ministry of Science and Technology, Taiwan 110-2320-B-039-033
6 · The paper itself

Abstract

Ribosome biogenesis is a cellular process critical for protein homeostasis during cell growth and multiplication. Our previous study confirmed up-regulation of ribosome biogenesis during endometriosis progression and malignant transition, thus anti-ribosome biogenesis may be effective for treating endometriosis and the associated complications. A mouse model with human endometriosis features was established and treated with three different drugs that can block ribosome biogenesis, including inhibitors against mTOR/PI3K (GSK2126458) and RNA polymerase I (CX5461 and BMH21). The average lesion numbers and disease frequencies were significantly reduced in treated mice as compared to controls treated with vehicle. Flow cytometry analyses confirmed the reduction of small peritoneal macrophage and neutrophil populations with increased large versus small macrophage ratios, suggesting inflammation suppression by drug treatments. Lesions in treated mice also showed lower nerve fiber density which can support the finding of pain-relief by behavioral studies. Our study therefore suggested ribosome biogenesis as a potential therapeutic target for treating endometriosis.

Indexed as

c-MYC/mTOR signalingendometriosisinflammationpainribosome biogenesisRNA polymerase 1

Identifiers

PMID35052864
PMCPMC8774031
OpenAlexW4206744723

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.