miR-142-3p as a Candidate Biomarker for Early-Stage Lung Adenocarcinoma: Integrative Bioinformatics Analysis and experimental Validation

Early-stage lung adenocarcinoma (LUAD) diagnosis is a clinical challenge. MicroRNAs (miRNAs) are identified as candidate biomarkers due to their regulatory role in cancer development. In this study, we performed a systematic analysis according to The Cancer Genome Atlas (TCGA) to identify differentially expressed miRNAs and mRNAs in LUAD. This was followed by network construction. We created a lncRNA-miRNA-mRNA regulatory network by identifying differentially expressed miRNAs and their target genes using information from TCGA, miR-TV database, and miRNET tool. miR-142-3p was identified as a candidate biomarker associated with LUAD development and patient survival. Our ceRNA network analysis identified four lncRNAs-LINC00689, MAGI2-AS3, DUBR, and LINC01719-as potential sponges of miR-142-3p in LUAD. RT-qPCR validation in paired tumors and adjacent normal tissues exhibited significantly higher expression of miR-142-3p in LUAD tissues. miR-142-3p also showed diagnostic potential through receiver operating characteristic (ROC) analysis (AUC = 0.8481). All the results implied that miR-142-3p can be a candidate biomarker for the early detection and diagnosis of LUAD.

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Publication Details

Journal
Biomarkers
Published
2025-10-27
DOI
https://doi.org/10.1080/1354750x.2025.2578000
Primary Topic
MicroRNA in disease regulation
Type
article
Field-Weighted Citation Impact
0.00
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article

miR-142-3p as a Candidate Biomarker for Early-Stage Lung Adenocarcinoma: Integrative Bioinformatics Analysis and experimental Validation

Mozhgan Sheikholeslami, Hamid Reza Soleimanpour‐Lichaei, Dor Mohammad Kordi-Tamandani, Saeideh Jafarinejad‐Farsangi
Biomarkers
MicroRNA in disease regulation
article

miR-142-3p as a Candidate Biomarker for Early-Stage Lung Adenocarcinoma: Integrative Bioinformatics Analysis and experimental Validation

Mozhgan Sheikholeslami, Hamid Reza Soleimanpour‐Lichaei, Dor Mohammad Kordi-Tamandani, Saeideh Jafarinejad‐Farsangi
article en

Abstract

Early-stage lung adenocarcinoma (LUAD) diagnosis is a clinical challenge. MicroRNAs (miRNAs) are identified as candidate biomarkers due to their regulatory role in cancer development. In this study, we performed a systematic analysis according to The Cancer Genome Atlas (TCGA) to identify differentially expressed miRNAs and mRNAs in LUAD. This was followed by network construction. We created a lncRNA-miRNA-mRNA regulatory network by identifying differentially expressed miRNAs and their target genes using information from TCGA, miR-TV database, and miRNET tool. miR-142-3p was identified as a candidate biomarker associated with LUAD development and patient survival. Our ceRNA network analysis identified four lncRNAs-LINC00689, MAGI2-AS3, DUBR, and LINC01719-as potential sponges of miR-142-3p in LUAD. RT-qPCR validation in paired tumors and adjacent normal tissues exhibited significantly higher expression of miR-142-3p in LUAD tissues. miR-142-3p also showed diagnostic potential through receiver operating characteristic (ROC) analysis (AUC = 0.8481). All the results implied that miR-142-3p can be a candidate biomarker for the early detection and diagnosis of LUAD.

Biomarkers
University of Sistan and Baluchestan (IR), Kerman University of Medical Sciences (IR), National Institute of Genetic Engineering and Biotechnology (IR)
Openalex Percentile: Top 62%
MicroRNA in disease regulation
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