Evidence map›Paper›PMID 30577586›Full record

ArticleInternational journal of molecular sciences2018

Lgr5 Does Not Vary Throughout the Menstrual Cycle in Endometriotic Human Eutopic Endometrium.

Júlia Vallvé-Juanico, Cristian Barón, Elena Suárez-Salvador, Josep Castellví, Agustín Ballesteros, Antonio Gil-Moreno, Xavier Santamaria

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

6 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Digestive system deep infiltrating endometriosis: What do we know.Journal of cellular and molecular medicine · 2023
    Review
  4. Article
  5. The Elusive Endometrial Epithelial Stem/Progenitor Cells.Frontiers in cell and developmental biology · 2021
    Review
  6. 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

7 authors at 4 institutions in 2 countries.

Júlia Vallvé-JuanicoDepartment of Reproductive Medicina, IVIRMA-Barcelona, 08017 Barcelona, Spain. julia.vallve@vhir.org.
Cristian BarónGroup of Biomedical Research in Gynecology, Vall Hebron Research Institute (VHIR) and University Hospital, 08035 Barcelona, Spain. crbaronv@gmail.com.
Elena Suárez-SalvadorDepartment of Gynecology, Vall d'Hebron University Hospital, 08035 Barcelona, Spain. elenafeb@yahoo.es.
Josep CastellvíDepartment of Pathology, Vall d'Hebron University Hospital, 08035 Barcelona, Spain. joscastellvi@vhebron.net.ORCID 0000-0001-5745-9996
Agustín BallesterosDepartment of Reproductive Medicina, IVIRMA-Barcelona, 08017 Barcelona, Spain. agustin.ballesteros@ivirma.com.
Antonio Gil-MorenoGroup of Biomedical Research in Gynecology, Vall Hebron Research Institute (VHIR) and University Hospital, 08035 Barcelona, Spain. antonioimma@yahoo.es.
Xavier SantamariaDepartment of Reproductive Medicina, IVIRMA-Barcelona, 08017 Barcelona, Spain. Xavier.santamaria@ivirma.com.
Vall d'Hebron Institut de Recerca · ESHebron University · PSBarcelona IVI Clinic · ESVall d'Hebron Hospital Universitari · ES

Funding

Centro Tecnologico Desarrollo Industrial IDI-2013039
6 · The paper itself

Abstract

Endometriosis is characterized by the abnormal presence of endometrium outside of the uterus, resulting in pelvic pain and infertility. The leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5) has been postulated to be a marker of stem cells in the endometrium. However, LGR5⁺ cells have a macrophage-like phenotype in this tissue, so it is unclear what role LGR5⁺ cells actually play in the endometrium. Macrophages serve an important function in the endometrium to maintain fertility, while LGR5⁺ cells generally have a role in tumor progression and are involved in invasion in some cancers. We sought to determine whether LGR5⁺ cells vary across the menstrual cycle in women with endometriosis and whether there are implications for LGR5 in the aggressiveness of endometriosis and reproductive outcomes. We performed immunofluorescence, flow cytometry, and primary culture in vitro experiments on eutopic and ectopic endometrium from healthy and endometriosis patients and observed that neither LGR5⁺ cells nor LGR5 expression varied throughout the cycle. Interestingly, we observed that LGR5⁺ cell percentage overexpressing CD163 (anti-inflammatory marker) was higher in healthy endometrium, suggesting that in endometriosis, endometrium presents a more pro-inflammatory phenotype that likely leads to poor obstetric outcomes. We also observed higher levels of LGR5⁺ cells in ectopic lesions compared to eutopic endometrium and specifically in deep infiltrating endometriosis, indicating that LGR5 could be involved in progression and aggressiveness of the disease.

Indexed as

Gene Expression RegulationBiomarkersCase-Control StudiesEndometriosisEndometriumFemaleFlow CytometryFluorescent Antibody TechniqueHumansMacrophagesMenstrual CycleReceptors, G-Protein-CoupledBiomarkersLGR5 protein, humanReceptors, G-Protein-CoupledendometriosisendometriumLGR5macrophagesmenstrual cycle

Identifiers

PMID30577586
PMCPMC6337520
OpenAlexW2906035180

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.