Evidence map›Paper›PMID 40160296›Full record

ArticleMolecular and clinical oncology2025

Diagnostic value of miR‑21 and miR‑221 as potential biomarkers for early diagnosis of prostate cancer.

Imane Mharrach, Kaoutar Anouar Tadlaoui, Mouna Aqerrout, Abdelilah Laraqui, Ahmed Ameur, Anouar El Ghazzaly, Khalid Ennibi, Moulay Mustapha Ennaji

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Article in Molecular and clinical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

8 authors.

Imane MharrachLaboratory of Virology, Oncology, Biosciences, Environment and New Energies, Faculty of Sciences and Techniques, Hassan II University of Casablanca, Casablanca 20650, Morocco.
Kaoutar Anouar TadlaouiLaboratory of Virology, Oncology, Biosciences, Environment and New Energies, Faculty of Sciences and Techniques, Hassan II University of Casablanca, Casablanca 20650, Morocco.
Mouna AqerroutLaboratory of Virology, Oncology, Biosciences, Environment and New Energies, Faculty of Sciences and Techniques, Hassan II University of Casablanca, Casablanca 20650, Morocco.
Abdelilah LaraquiRoyal School of Military Health Service, Sequencing Unit, Laboratory of Virology, Center of Virology, Infectious and Tropical Diseases, Mohammed V Military Teaching Hospital, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat 10000, Morocco.
Ahmed AmeurDepartment of Urology, Mohammed V Military Teaching Hospital, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat 10000, Morocco.
Anouar El GhazzalyDepartment of Urology, Mohammed V Military Teaching Hospital, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat 10000, Morocco.
Khalid EnnibiCenter of Virology, Infectious and Tropical Diseases, Mohammed V Military Teaching Hospital, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat 10000, Morocco.
Moulay Mustapha EnnajiLaboratory of Virology, Oncology, Biosciences, Environment and New Energies, Faculty of Sciences and Techniques, Hassan II University of Casablanca, Casablanca 20650, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer (PCa) is globally the second most diagnosed malignancy in men, with >1.5 million new cases reported in 2020. Given the limitations of classical detection methods, the discovery of new predictive PCa biomarkers is critical. MicroRNAs (miRs), which are small, single-stranded, non-coding RNA molecules, have emerged as potential biomarkers for cancer diagnosis and prognosis. The present study aimed to evaluate the diagnostic value of miR-21 and miR-221 in PCa and their association with clinicopathological parameters. The expression of miR-21 and miR-221 was assessed using reverse transcription-quantitative PCR in 50 tumour and 50 control tissue samples. The results demonstrated that miR-21 and miR-221 were significantly upregulated in PCa tissues compared with that of the normal control tissues. Receiver operating characteristic curve analysis revealed that miR-21 had an area under the curve (AUC) of 0.90, with a sensitivity of 70% and a specificity of 96%. Similarly, miR-221 demonstrated an AUC of 0.89, with a sensitivity of 86% and a specificity of 78%. High expression of miR-21 and miR-221 was also demonstrated to be associated with higher Gleason scores and advanced tumour stages. The findings of the present study indicate the potential role of miR-21 and miR-221 as biomarkers in the diagnosis of PCa. However, further studies in non-invasive samples such as serum, blood and urine are needed to support the results of the present study.

Indexed as

biomarkerclinicopathological featuresdiagnosismicroRNA-21microRNA-221prostate cancerreverse transcription-quantitative PCR

Identifiers

PMID40160296
PMCPMC11948486

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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.