Evidence map›Paper›PMID 39579091›Full record

ReviewMolecular human reproduction2024

mTOR inhibitors as potential therapeutics for endometriosis: a narrative review.

Akiko Nakamura, Yuji Tanaka, Tsukuru Amano, Akie Takebayashi, Akimasa Takahashi, Tetsuro Hanada, Shunichiro Tsuji, Takashi Murakami

Abstract readReview
In one paragraph

Review in Molecular human reproduction, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  10. Review
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  15. Endometriosis and autoimmunity.Autoimmunity reviews · 2025
    Review
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  17. 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

8 authors.

Akiko NakamuraDepartment of Obstetrics and Gynaecology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Yuji TanakaDepartment of Obstetrics and Gynaecology, Shiga University of Medical Science, Otsu, Shiga, Japan.ORCID 0000-0002-7045-8151
Tsukuru AmanoDepartment of Obstetrics and Gynaecology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Akie TakebayashiDepartment of Obstetrics and Gynaecology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Akimasa TakahashiDepartment of Obstetrics and Gynaecology, Shiga University of Medical Science, Otsu, Shiga, Japan.ORCID 0000-0001-5698-553X
Tetsuro HanadaDepartment of Obstetrics and Gynaecology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Shunichiro TsujiDepartment of Obstetrics and Gynaecology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Takashi MurakamiDepartment of Obstetrics and Gynaecology, Shiga University of Medical Science, Otsu, Shiga, Japan.ORCID 0000-0002-0250-0856

Funding

Japan Society for the Promotion of ScienceJSPS KAKENHI 21K09493
6 · The paper itself

Abstract

Mammalian target of rapamycin (mTOR) inhibitors have been used clinically as anticancer and immunosuppressive agents for over 20 years, demonstrating their safety after long-term administration. These inhibitors exhibit various effects, including inhibition of cell proliferation, interaction with the oestrogen and progesterone pathways, immunosuppression, regulation of angiogenesis, and control of autophagy. We evaluated the potential of mTOR inhibitors as therapeutic agents for endometriosis, examined the secondary benefits related to reproductive function, and assessed how their side effects can be managed. We conducted a thorough review of publications on the role of the mTOR pathway and the effectiveness of mTOR inhibitors in endometriosis patients. These results indicate that the mTOR pathway is activated in endometriosis. Additionally, mTOR inhibitors have shown efficacy as monotherapies for endometriosis. They may alleviate resistance to hormonal therapy in endometriosis, suggesting a potential synergistic effect when used in combination with hormonal therapy. The potential reproductive benefits of mTOR inhibitors include decreased miscarriage rates, improved implantation, and prevention of age-related follicular loss and ovarian hyperstimulation syndrome. Activation of the mTOR pathway has also been implicated in the malignant transformation of endometriosis. Preclinical studies suggest that the dosage of mTOR inhibitors needed for treating endometriosis may be lower than that required for anticancer or immunosuppressive therapy, potentially reducing dosage-dependent side effects. In conclusion, while mTOR inhibitors, which allow for pregnancy during oral administration, show potential for clinical use in all stages of endometriosis, current evidence is limited to preclinical studies, and further research is needed to confirm clinical effectiveness.

Indexed as

EndometriosisMTOR InhibitorsTOR Serine-Threonine KinasesAnimalsFemaleHumansPregnancySignal TransductionMTOR InhibitorsMTOR protein, humanTOR Serine-Threonine Kinasesadenomyosisendometriosiseverolimusfertility preservationhormonal resistancemTOR inhibitorrapamycinsirolimus

Identifiers

PMID39579091
PMCPMC11634386

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.