Evidence map›Paper›PMID 40141259›Full record

ArticleInternational journal of molecular sciences2025

MiR-205-5p and MiR-222-3p as Potential Biomarkers of Endometrial Cancer.

Anna Bogaczyk, Natalia Potocka, Sylwia Paszek, Marzena Skrzypa, Alina Zuchowska, Michał Kośny, Marta Kluz-Barłowska, Andrzej Wróbel, Jan Wróbel, Izabela Zawlik and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

11 authors.

Anna BogaczykDepartment of Gynecology, Gynecology Oncology and Obstetrics, Fryderyk Chopin University Hospital, 35-055 Rzeszow, Poland.ORCID 0009-0008-8816-0290
Natalia PotockaLaboratory of Molecular Biology, Centre for Innovative Research in Medical and Natural Sciences, Faculty of Medicine, Collegium Medicum, University of Rzeszow, 35-959 Rzeszow, Poland.ORCID 0000-0002-5505-3922
Sylwia PaszekFaculty of Medicine, Collegium Medicum, University of Rzeszow, 35-959 Rzeszow, Poland.ORCID 0000-0002-7865-2661
Marzena SkrzypaLaboratory of Molecular Biology, Centre for Innovative Research in Medical and Natural Sciences, Faculty of Medicine, Collegium Medicum, University of Rzeszow, 35-959 Rzeszow, Poland.
Alina ZuchowskaFaculty of Medicine, Collegium Medicum, University of Rzeszow, 35-959 Rzeszow, Poland.
Michał KośnyDepartment of Hematology, Medical University of Lodz, 90-419 Lodz, Poland.
Marta Kluz-BarłowskaDepartment of Pathology, Fryderyk Chopin University Hospital, 35-055 Rzeszow, Poland.ORCID 0000-0003-4100-4924
Andrzej WróbelSecond Department of Gynecology, Medical University of Lublin, Jaczewskiego 8, 20-090 Lublin, Poland.ORCID 0000-0002-5772-0573
Jan WróbelMedical Faculty, Medical University of Lublin, 20-090 Lublin, Poland.ORCID 0009-0008-4168-9410
Izabela ZawlikLaboratory of Molecular Biology, Centre for Innovative Research in Medical and Natural Sciences, Faculty of Medicine, Collegium Medicum, University of Rzeszow, 35-959 Rzeszow, Poland.
Tomasz KluzDepartment of Gynecology, Gynecology Oncology and Obstetrics, Fryderyk Chopin University Hospital, 35-055 Rzeszow, Poland.ORCID 0000-0002-4798-3986

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endometrial cancer is the fourth most common cancer in women in Europe. Its carcinogenesis is a complex process and requires further research. In our study, we focus on finding new and easy-to-diagnose markers for detecting endometrial cancer. For this purpose, we compared the levels of miR-21-5p, miR-205-5p, and miR-222-3p in endometrial cancer tissues with the levels of these miRs in the serum of patients using the dPCR method. Our study is preliminary and consists of comparing the changes in miRNA expression in serum to the changes in miRNA in tissue of patients with endometrial cancer. The study included 18 patients with EC and 19 patients undergoing surgery for pelvic organ prolapse or uterine fibroids as a control group without neoplastic lesions. Endometrial tissue and serum were collected from all patients. The analyses showed an increased expression of miR-205-5p in endometrial cancer tissue and decreased expression of miR-222-3p in tissue and serum samples. These results suggest that miR-205-5p and miR-222-3p may be potential endometrial cancer biomarkers. Only miR-222-3p confirmed its decreased expression in serum, making it a potential and easily accessible marker in the diagnosis of endometrial cancer. This pilot study requires further investigation in a larger group of patients. Its advantages include the possibility of a comparison between miRNA expression in tissue and serum, as well as conducting the study using dPCR.

Indexed as

Biomarkers, TumorEndometrial NeoplasmsMicroRNAsAdultAgedFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedBiomarkers, TumorMicroRNAsMIR205, humanMIR222, humanbiomarkersdigitalPCRdPCRECendometrium cancermicroRNAmiR-205-5pmiR-21-5pmiR-222-3p

Identifiers

PMID40141259
PMCPMC11941963

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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.