Evidence map›Paper›PMID 36369244›Full record

ArticleCommunications biology2022

Niclosamide targets the dynamic progression of macrophages for the resolution of endometriosis in a mouse model.

Liang Zhao, Mingxin Shi, Sarayut Winuthayanon, James A MacLean, Kanako Hayashi

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
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  11. Article
  12. Article
  13. New Potential Pharmacological Options for Endometriosis Associated Pain.International journal of molecular sciences · 2024
    Review
  14. Article
  15. The involvement of peritoneal GATA6Frontiers in immunology · 2024
    Article
  16. Article
  17. Article
  18. 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

5 authors at 1 institution in 1 country.

Liang ZhaoSchool of Molecular Biosciences, Center for Reproductive Biology, Washington State University, Pullman, Washington, 99164, USA.
Mingxin ShiSchool of Molecular Biosciences, Center for Reproductive Biology, Washington State University, Pullman, Washington, 99164, USA.
Sarayut WinuthayanonSchool of Molecular Biosciences, Center for Reproductive Biology, Washington State University, Pullman, Washington, 99164, USA.ORCID 0000-0002-8439-0389
James A MacLeanSchool of Molecular Biosciences, Center for Reproductive Biology, Washington State University, Pullman, Washington, 99164, USA.ORCID 0000-0003-3061-150X
Kanako HayashiSchool of Molecular Biosciences, Center for Reproductive Biology, Washington State University, Pullman, Washington, 99164, USA. k.hayashi@wsu.edu.ORCID 0000-0002-5028-799X
Washington State University · US

Funding

Complex inflammatory mechanisms and therapeutic targeting in endometriosisR01HD104619 · NICHD · WASHINGTON STATE UNIVERSITY · PI HAYASHI, KANAKO · 2021 to 2025
$2.4M
NICHD NIH HHS R01 HD104619
6 · The paper itself

Abstract

Due to the vital roles of macrophages in the pathogenesis of endometriosis, targeting macrophages could be a promising therapeutic direction. Here, we investigated the efficacy of niclosamide for the resolution of a perturbed microenvironment caused by dysregulated macrophages in a mouse model of endometriosis. Single-cell transcriptomic analysis revealed the heterogeneity of macrophages including three intermediate subtypes with sharing characteristics of traditional "small" or "large" peritoneal macrophages (SPMs and LPMs) in the peritoneal cavity. Endometriosis-like lesions (ELL) enhanced the differentiation of recruited macrophages, promoted the replenishment of resident LPMs, and increased the ablation of embryo-derived LPMs, which were stepwise suppressed by niclosamide. In addition, niclosamide restored intercellular communications between macrophages and B cells. Therefore, niclosamide rescued the perturbed microenvironment in endometriosis through its fine regulations on the dynamic progression of macrophages. Validation of similar macrophage pathogenesis in patients will further promote the clinical usage of niclosamide for endometriosis treatment.

Indexed as

EndometriosisAnimalsDisease Models, AnimalFemaleHumansMacrophagesMacrophages, PeritonealMiceNiclosamideNiclosamide

Identifiers

PMID36369244
PMCPMC9652344
OpenAlexW4308792166

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.