ArticleTranslational cancer research2025
Potential biomarker for screening nasopharyngeal carcinoma: three-microRNA panel in serum.
Article in Translational cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- APOA1, DEFB103A_DEFB103B and DSG3 Are Novel Circulating Biomarkers of Psoriasis.International journal of molecular sciences · 2026Article
- Development and validation of a machine learning model for predicting 3-year overall survival in metastatic nasopharyngeal carcinoma: a SEER database and web visualization study.Translational cancer research · 2025Article
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9 authors.
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Abstract
Background: Nasopharyngeal carcinoma (NPC) is a prevalent form of cancer in Southeast Asia, characterized by distinctive epidemiological attributes, and its occurrence is influenced by factors such as race, age, and gender. Prior research has highlighted the potential of serum microRNA (miRNA) profiling as a non-invasive biomarker for cancer detection. The objective of this study was to ascertain the miRNAs that are specifically linked to the diagnosis of NPC. Methods: A three-phase study was conducted, involving a total of 112 participants (56 NPC patients and 56 healthy controls). Reverse transcription quantitative polymerase chain reaction (RT-qPCR) was employed to measure the expression levels of miRNAs in NPCs and healthy controls (HCs). The diagnostic capability of serum miRNAs for NPCs was assessed using receiver operating characteristic (ROC) curves and the area under the ROC curve (AUC). Furthermore, a diagnostic panel consisting of three miRNAs with high efficiency was constructed using inverse stepwise logistic regression. In addition, we investigated the biological functions of candidate miRNAs. Results: When compared to healthy controls, the blood of NPC patients had significantly dysregulated levels of five miRNAs (hsa-miR-363-3p, hsa-miR-106a-5p, hsa-miR-20b-5p, hsa-miR-200a-3p, hsa-miR-200b-3p). In order to create the diagnostic panels, hsa-miR-20b-5p, hsa-miR-200b-3p and hsa-miR-106a-5p were used. The panel's AUC was 0.925 [95% confidence interval (CI): 0.858-0.967; P<0.001; sensitivity: 94.64%; specificity: 76.92%]. According to the Gene Expression Profiling Interactive Analysis (GEPIA) database results, the target genes Conclusions: Our three-miRNA panel (hsa-miR-20b-5p, hsa-miR-200b-3p and hsa-miR-106a-5p) is anticipated to be a promising non-invasive biomarker for NPC screening and diagnosis.
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