Evidence map›Paper›PMID 42294619›Full record

ReviewExpert reviews in molecular medicine2026

RAGE-Mediated Signalling in Gynaecological Disorders: Review of Molecular Mechanisms and Therapeutic Perspectives.

Krzysztof Łuszczyński, Magdalena Dec, Aleksander Chodowiec, Marcin Radziszewski, Robert Zdanowski, Monika Szafarowska, Paweł Kamiński, Paweł Włodarski, Anna Lutyńska, Aneta Ścieżyńska

Abstract readReview
In one paragraph

Review in Expert reviews in molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Krzysztof ŁuszczyńskiLaboratory of Molecular Oncology and Innovative Therapies, https://ror.org/04zvqhj72Military Institute of Medicine National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.
Magdalena DecLaboratory of Molecular Oncology and Innovative Therapies, https://ror.org/04zvqhj72Military Institute of Medicine National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.
Aleksander ChodowiecLaboratory of Molecular Oncology and Innovative Therapies, https://ror.org/04zvqhj72Military Institute of Medicine National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.
Marcin RadziszewskiLaboratory of Molecular Oncology and Innovative Therapies, https://ror.org/04zvqhj72Military Institute of Medicine National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.ORCID 0000-0002-9664-3099
Robert ZdanowskiLaboratory of Molecular Oncology and Innovative Therapies, https://ror.org/04zvqhj72Military Institute of Medicine National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.ORCID 0000-0003-0455-1072
Monika SzafarowskaDepartment of Gynecology and Oncological Gynecology, https://ror.org/04zvqhj72Military Institute of Medicine National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.
Paweł KamińskiDepartment of Gynecology and Oncological Gynecology, https://ror.org/04zvqhj72Military Institute of Medicine National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.
Paweł WłodarskiDepartment of Histology and Embryology, https://ror.org/04p2y4s44Medical University of Warsaw, 02-004 Warsaw, Poland.
Anna LutyńskaLaboratory of Molecular Oncology and Innovative Therapies, https://ror.org/04zvqhj72Military Institute of Medicine National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.
Aneta ŚcieżyńskaLaboratory of Molecular Oncology and Innovative Therapies, https://ror.org/04zvqhj72Military Institute of Medicine National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.ORCID 0000-0003-0438-2678

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe receptor for advanced glycation end-products (RAGE) is a unique multi-ligand member of the immunoglobulin superfamily that exists in both membrane-bound and soluble forms. Under physiological conditions, RAGE expression is low in most tissues; however, it is markedly upregulated in response to tissue injury, inflammation or metabolic stress. Ligand-induced activation of RAGE initiates complex intracellular signalling cascades that regulate inflammation, extracellular matrix remodelling, cell proliferation, survival and migration.

methodsWhile the contribution of RAGE to diabetes and chronic inflammatory diseases is well established, its role in gynaecological disorders remains insufficiently characterized.

resultsThis comprehensive review summarizes current evidence on the involvement of RAGE in the pathogenesis of benign gynaecological disorders, such as endometriosis and polycystic ovary syndrome (PCOS), pregnancy-related complications and malignant neoplasms of the female reproductive tract.

conclusionsIt also discusses emerging therapeutic strategies aimed at targeting the RAGE pathway, highlighting their potential translational relevance in gynaecological practice.

Indexed as

EndometriosisGenital Diseases, FemalePolycystic Ovary SyndromeReceptor for Advanced Glycation End ProductsSignal TransductionAnimalsFemaleGlycation End Products, AdvancedHumansPregnancyGlycation End Products, AdvancedReceptor for Advanced Glycation End ProductsAGEscancerglycationgynaecologyinflammationpregnancyRAGEtargeted therapy

Identifiers

PMID42294619
PMCPMC13472240

What Socratic holds

Textmetadata
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 Socratic graph.