Evidence map›Paper›PMID 40266039›Full record

ArticleEinstein (Sao Paulo, Brazil)2025

Comparative analysis of miRNA-mRNA interaction prediction tools based on experimental head and neck cancer data.

Bárbara Dos Santos Dias, Larissa Figueiredo Alves Diniz, Lucca D'Arco Corrêa, Rafael Pereira de Souza, Leticia Torres Ferreira, Denise da Cunha Pasqualin, Rafael de Cicco, Eloiza Helena Tajara da Silva, Patricia Severino

Abstract readComparative Study
In one paragraph

Article in Einstein (Sao Paulo, Brazil), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. QMRInternational journal of molecular sciences · 2025
    Article
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

9 authors.

Bárbara Dos Santos DiasHospital Israelita Albert Einstein, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0004-5643-4518
Larissa Figueiredo Alves DinizHospital Israelita Albert Einstein, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-3094-661X
Lucca D'Arco CorrêaHospital Israelita Albert Einstein, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0006-3521-0800
Rafael Pereira de SouzaInstituto do Câncer Dr. Arnaldo Vieira de Carvalho, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0001-5916-9730
Leticia Torres FerreiraHospital Israelita Albert Einstein, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0008-4061-1443
Denise da Cunha PasqualinHospital Israelita Albert Einstein, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-0087-6347
Rafael de CiccoInstituto do Câncer Dr. Arnaldo Vieira de Carvalho, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-2505-0461
Eloiza Helena Tajara da SilvaFaculdade de Medicina de São José do Rio Preto, São Jose do Rio Preto, SP, Brazil.ORCID http://orcid.org/0000-0002-2603-2057
Patricia SeverinoHospital Israelita Albert Einstein, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-6682-9343

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe evaluated the performance of TargetScan, miRDB, and miRWalk for predicting miRNA-mRNA interactions in HNSCC. Based on clinical tumor and cancer-free tissue data, miRWalk emerged as the most comprehensive tool. Validation using NanoString technology and MiRTarBase confirmed key predictions, highlighting the important roles of the PI3K-Akt and Wnt pathways. This study underscores the importance of integrating bioinformatics and experimental data to better understand HNSCC.

background■ miRWalk had the highest predicted interactions and validated miRNA networks in HNSCC.

background■ Around 3.3% of interactions overlapped across tools, emphasizing the need for multitool approaches.

background■ Dysregulated genes and miRNAs were tied to cancerdriving PI3K-Akt and Wnt pathways.

background■ The validated approach highlights the importance of integrating computational and molecular data.

objectiveHead and neck squamous cell carcinoma (HNSCC) has a poor prognosis largely due to late diagnosis and a lack of reliable biomarkers. MicroRNAs (miRNAs), small non-coding RNAs that regulate gene expression, are promising biomarkers for HNSCC. This study evaluated miRNA-mRNA interactions in HNSCC using conventional computational tools and validated the results using molecular data.

methodsWe compared three miRNA-mRNA interaction prediction tools, TargetScan, miRDB, and miRWalk, using differentially expressed miRNAs and mRNAs from HNSCC and cancer-free tissues. NanoString nCounter was used to measure miRNA and mRNA expression and the miRTarBase database was used to validate the predicted miRNA-mRNA interactions.

resultsTargetScan and miRWalk provide a comprehensive overview of potential interactions, whereas miRDB provides functional insights. Our results identified 77 and 154 differentially expressed miRNAs and mRNAs in HNSCC, respectively. miRWalk predicted the highest number of miRNA-mRNA interactions, followed by miRDB and TargetScan. Only 3.3% of interactions were common among the tools. The MiRTarBase analysis confirmed a small subset of the predictions. Biological pathway analysis highlighted the dysregulation of PI3K-Akt and Wnt signaling; miRWalk was the best for elucidating how miRNAs modulate target mRNAs in these key pathways during HNSCC progression.

conclusionmiRWalk emerged as the most robust tool for predicting miRNA-mRNA interactions. Our findings highlight the importance of integrating bioinformatics predictions with experimental data to better understand the regulatory networks in HNSCC and identify potential biomarkers for diagnosis and therapy.

Indexed as

Computational BiologyHead and Neck NeoplasmsMicroRNAsRNA, MessengerSquamous Cell Carcinoma of Head and NeckBiomarkers, TumorGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansBiomarkers, TumorMicroRNAsRNA, Messenger

Identifiers

PMID40266039
PMCPMC12061445

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.