Evidence map›Paper›PMID 39215008›Full record

ArticleScientific reports2024

miR-21, miR-29a, and miR-106b: serum and tissue biomarkers with diagnostic potential in metastatic testicular cancer.

Zsuzsanna Ujfaludi, Fruzsina Fazekas, Krisztina Biró, Orsolya Oláh-Németh, Istvan Buzogany, Farkas Sükösd, Tamás Beöthe, Tibor Pankotai

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Family-Based Study RevealsInternational journal of molecular sciences · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. MicroRNA-Mediated Regulatory Networks inBiochemistry research international · 2025
    Review
  6. Article
  7. 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

8 authors.

Zsuzsanna Ujfaludi *Department of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Fruzsina Fazekas *Department of Urology, Péterfy Sándor street Hospital and Clinic, Budapest, Hungary.
Krisztina BiróDepartment of Genitourinary Oncology and Clinical Pharmacology, National Institute of Oncology, Budapest, Hungary.
Orsolya Oláh-NémethDepartment of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Istvan BuzoganyDepartment of Urology, Péterfy Sándor street Hospital and Clinic, Budapest, Hungary.
Farkas SükösdDepartment of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Tamás BeötheDepartment of Urology, Péterfy Sándor street Hospital and Clinic, Budapest, Hungary. tamasbeothe@gmail.com.
Tibor PankotaiDepartment of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary. pankotai.tibor@szte.hu.

Funding

EU's Horizon 2020 Research and Innovation Program 739593Magyar Tudományos Akadémia POST-COVID2021-36National Research, Development and Innovation Fund TKP-2021-EGA-05National Research, Development and Innovation Office grant NKFI-FK 132080
6 · The paper itself

Abstract

The imperative need for sensitive and precise tools is underscored in cancer diagnostics, with biomarkers playing a pivotal role in facilitating early detection and tumor diagnosis. Despite their classical pathological classification, testicular tumors lack valuable markers, emphasizing the necessity to identify and apply serum tumor markers in clinical management. Unfortunately, existing biomarkers exhibit limited sensitivities and specificities. Recent years have witnessed the discovery of novel RNA molecules, presenting a potential breakthrough as diagnostic tools and promising biomarkers. This report presents compelling evidence supporting the detection of early testicular cancer by applying a set of nine microRNAs (miRNAs), establishing them as valuable serum biomarkers for diagnosis. We developed a standardized serum-based measurement protocol and conducted comprehensive statistical analyses on the dataset to underscore the diagnostic accuracy of the miRNA pool. Notably, with a sensitivity exceeding 93%, miR-21, miR-29a, and miR-106b surpass classical serum tumor markers in the context of testicular cancer. Specifically, these miRNAs are poised to enhance clinical decision-making in testicular cancer detection and hold the potential for assessing tumor growth in monitoring chemotherapy outcomes.

Indexed as

Biomarkers, TumorMicroRNAsTesticular NeoplasmsAdultGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm MetastasisBiomarkers, TumorMicroRNAsMIRN106 microRNA, humanMIRN21 microRNA, humanMIRN29a microRNA, humanBiomarkerCancer diagnosticsMiR-106bMiR-21MiR-29aMiRNATesticular cancer

Identifiers

PMID39215008
PMCPMC11364861

What Socratic holds

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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 Socratic graph.