Evidence map›Paper›PMID 40135061›Full record

ArticleReproductive medicine and biology

Combined targeting of TCF7L1/2, PTEN, CDK6, and BCCIP by microRNA miR-29c-3p is associated with reduced invasion and proliferation of endometriotic cells.

Teresa Helene Wentges, Heba M El-Shorafa, Janine Beckmann, Michael Gabriel, Matti Poutanen, Burkhard Greve, Ludwig Kiesel, Sebastian D Schäfer, Martin Götte

Abstract read
In one paragraph

Article in Reproductive medicine and biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Therapeutic Potential ofInternational journal of molecular sciences · 2026
    Article
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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

9 authors.

Teresa Helene WentgesDepartment of Gynecology and Obstetrics Münster University Hospital, Research Laboratory Münster Germany.
Heba M El-ShorafaDepartment of Gynecology and Obstetrics Münster University Hospital, Research Laboratory Münster Germany.
Janine BeckmannDepartment of Gynecology and Obstetrics Münster University Hospital, Research Laboratory Münster Germany.
Michael GabrielDepartment of Obstetrics and Gynecology Institute of Medicine, University of Turku Turku Finland.
Matti PoutanenResearch Centre for Integrative Physiology and Pharmacology Institute of Biomedicine, University of Turku Turku Finland.
Burkhard GreveDepartment of Radiotherapy-Radiooncology Münster University Hospital Münster Germany.
Ludwig KieselDepartment of Gynecology and Obstetrics Münster University Hospital, Research Laboratory Münster Germany.
Sebastian D SchäferDepartment of Gynecology and Obstetrics Münster University Hospital, Research Laboratory Münster Germany.
Martin GötteDepartment of Gynecology and Obstetrics Münster University Hospital, Research Laboratory Münster Germany.ORCID https://orcid.org/0000-0003-2360-2496

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Endometriosis is a chronic gynecological disorder associated with pain symptoms and infertility. The expression of microRNA miR-29c-3p is dysregulated in endometriosis. We aimed to identify novel molecular targets of miR-29c-3p functionally linked to proliferation and invasive growth in endometriosis. Methods: The epithelial endometriotic cell line 12Z and primary endometriotic stromal cells (PESC) were transfected with control miRNA or pre-miR-29c-3p, and subjected to cell cycle analysis, cell viability, wound healing, and Matrigel invasion assays. Expression of bioinformatically predicted miR-29c-3p targets was analyzed by qPCR and western blot. Target gene expression in endometriotic lesions and healthy endometrium was studied in the EndometDB endometriosis database. Results: miR-29c-3p decreased 12Z and PESC cell viability and the proportion of PESC in the S-phase. 12Z cell invasion, but not migration, was decreased after miR-29c-3p upregulation. miR-29c-3p decreased the mRNA expression of Conclusions: miR-29c-3p effectively curbs endometriotic cell proliferation and invasion by combined inhibition of cell cycle regulators and transcription factors, unveiling a promising therapeutic strategy.

Indexed as

CDK6endometriosismicroRNAmiR‐29cp21

Identifiers

PMID40135061
PMCPMC11933757

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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.