Evidence map›Paper›PMID 41152570›Full record

ArticleThe Journal of pathology2026

MicroRNA profiling of testicular Leydig cell tumors identifies a microRNA signature associated with malignancy and miR-196b-5p as a potentially useful biomarker.

João Lobo, Nuno Tiago Tavares, Fernanda Fernandes-Pontes, Vera Constâncio, Ana Teixeira Marques, Bruno Oliveira-Lopes, Diana Fonseca, Carmen Jerónimo, Rui Henrique, Kvetoslava Michalova and 13 more

Abstract read
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Article in The Journal of pathology, 2026. 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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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

23 authors.

João Lobo *Department of Pathology, Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC), R. Dr. António Bernardino de Almeida, Porto, Portugal.ORCID https://orcid.org/0000-0001-6829-1391
Nuno Tiago Tavares *Cancer Biology and Epigenetics Group, IPO Porto Research Center (GEBC CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC) & CI-IPOP@RISE (Health Research Network), R. Dr. António Bernardino de Almeida, Porto, Portugal.
Fernanda Fernandes-PontesCancer Biology and Epigenetics Group, IPO Porto Research Center (GEBC CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC) & CI-IPOP@RISE (Health Research Network), R. Dr. António Bernardino de Almeida, Porto, Portugal.ORCID https://orcid.org/0009-0007-3931-0443
Vera ConstâncioCancer Biology and Epigenetics Group, IPO Porto Research Center (GEBC CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC) & CI-IPOP@RISE (Health Research Network), R. Dr. António Bernardino de Almeida, Porto, Portugal.
Ana Teixeira MarquesCancer Biology and Epigenetics Group, IPO Porto Research Center (GEBC CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC) & CI-IPOP@RISE (Health Research Network), R. Dr. António Bernardino de Almeida, Porto, Portugal.
Bruno Oliveira-LopesCancer Biology and Epigenetics Group, IPO Porto Research Center (GEBC CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC) & CI-IPOP@RISE (Health Research Network), R. Dr. António Bernardino de Almeida, Porto, Portugal.
Diana FonsecaCancer Biology and Epigenetics Group, IPO Porto Research Center (GEBC CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC) & CI-IPOP@RISE (Health Research Network), R. Dr. António Bernardino de Almeida, Porto, Portugal.
Carmen JerónimoCancer Biology and Epigenetics Group, IPO Porto Research Center (GEBC CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC) & CI-IPOP@RISE (Health Research Network), R. Dr. António Bernardino de Almeida, Porto, Portugal.
Rui HenriqueDepartment of Pathology, Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (P.CCC), R. Dr. António Bernardino de Almeida, Porto, Portugal.
Kvetoslava MichalovaDepartment of Pathology, Charles University, Faculty of Medicine in Plzen, Bioptical Laboratory, Ltd, Pilsen, Czech Republic.ORCID https://orcid.org/0000-0003-3231-6870
Kristine M CornejoDepartment of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Maurizio ColecchiaDepartment of Pathology, Vita-Salute San Raffaele University, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Costantino RicciPathology Unit, DIAP-Dipartimento Interaziendale di anatomia patologica di Bologna, Maggiore Hospital-AUSL Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0001-7254-4195
Muhammad T IdreesDepartment of Pathology, Indiana University, Indianapolis, IN, USA.
Felix ContrerasLaboratorio de Patología, Clínica Universitaria Unión Médica, PUCMM, Santiago, Dominican Republic.
Isabel M Fernandez GonzalezLaboratorio de Patología, Clínica Universitaria Unión Médica, PUCMM, Santiago, Dominican Republic.
William J AndersonDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Fiona MacLeanDouglass Hanly Moir Pathology, Macquarie Park, NSW, Australia.
Adeboye O OsunkoyaDepartment of Pathology and Urology, Emory University School of Medicine, Atlanta, GA, USA.
Chia-Sui KaoDepartment of Pathology and Laboratory Medicine, Cleveland Clinic Foundation, Cleveland, OH, USA.
Ankur R SangoiDepartment of Pathology, Stanford University, Stanford, CA, USA.
Thomas M UlbrightDepartment of Pathology, Indiana University, Indianapolis, IN, USA.
Andres M AcostaDepartment of Pathology, Indiana University, Indianapolis, IN, USA.ORCID https://orcid.org/0000-0001-8817-6331

Funding

Fundação para a Ciência e a Tecnologia 2022.09566.BD
6 · The paper itself

Abstract

Approximately 10% of testicular Leydig cell tumors (LCTs) are clinically malignant and unresponsive to systemic treatment. Predicting their clinical behavior can be problematic because there are no biomarkers that can consistently discriminate between benign and malignant LCTs. We assessed microRNA expression profiles of LCTs to identify differentially expressed microRNAs that could potentially distinguish benign from malignant neoplasms. The study consisted of two phases. In the first (discovery) phase, we interrogated 768 microRNAs in a series of 11 LCTs (six malignant and five benign) using Taqman Low-Density Array (TLDA) microRNA profiling. In the second phase, we validated the top differentially expressed microRNA targets with real-time quantitative PCR on a series of 35 LCTs (17 malignant and 18 benign), assessing their clinical performance for distinguishing malignant from benign LCTs. Target biologic pathways were analyzed using the miRTargetLink 2.0 tool. A total of 50 microRNAs were differentially regulated in malignant LCTs (27 upregulated, 23 downregulated). The top six microRNA candidates (top three upregulated and top three downregulated) were validated, showing good performance for discriminating between malignant and benign LCTs, with an area under the curve (AUC) ranging between 0.69 and 0.87. MiR-196b-5p showed the best performance, with sensitivity, specificity, negative predictive value, positive predictive value, and accuracy of 82%, 83%, 83%, 82%, and 83%, respectively. A panel (i.e. combined) analysis reached 100% sensitivity and 83% specificity. Pathway analysis revealed significant overlap in the biological process targeted by the upregulated microRNAs in malignant LCTs, including proliferation, development, metabolism, hormone synthesis, and cell death. Our results support the idea that malignant LCTs are associated with a distinct microRNA signature. MiR-196b-5p was identified as a potentially useful biomarker to distinguish benign from malignant tumors. The shared downstream targets of the top upregulated microRNAs suggest that dysregulation of cell proliferation and apoptosis underlie aggressive biologic behavior in LCTs and may offer opportunities for targeted therapies. © 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Indexed as

Biomarkers, TumorGene Expression ProfilingLeydig Cell TumorMicroRNAsTesticular NeoplasmsAdultGene Expression Regulation, NeoplasticHumansMaleMiddle AgedReal-Time Polymerase Chain ReactionYoung AdultBiomarkers, TumorMicroRNAsMIRN196 microRNA, humanbiomarkersLeydig cell tumorsmalignantmicroRNAsrisk stratificationsex cord stromal tumors

Identifiers

PMID41152570
PMCPMC12699239

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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.