Evidence map›Paper›PMID 42104044›Full record

ArticleMolecular imaging and biology2026

Clinical Effectiveness of miR-760 to Distinguish Benign and Malignant Pulmonary Nodules on the Basis of Low-Dose Spiral CT Imaging.

Jianwen Chen, Fei Li, Jianguang Chen, Quanxing Li, Yujie Ren, Ruibao Liu

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Article in Molecular imaging and biology, 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jianwen ChenMedical Department, Dongying People's Hospital, Dongying, 257091, Shandong, China. chenjianwen2117@163.com.
Fei LiDepartment of Medical Imaging, Dongying People's Hospital, Dongying, 257091, Shandong, China.
Jianguang ChenDepartment of Cardiothoracic Surgery, Dongying People's Hospital, Dongying, 257091, Shandong, China.
Quanxing LiDepartment of Cardiothoracic Surgery, Dongying People's Hospital, Dongying, 257091, Shandong, China.
Yujie RenDepartment of Medical Imaging, Dongying People's Hospital, Dongying, 257091, Shandong, China.
Ruibao LiuDepartment of Oncology, Dongying People's Hospital, Dongying, 257091, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe differential diagnosis of benign and malignant pulmonary nodules is a key problem in clinical diagnosis. Low-dose spiral CT (LDCT) is a commonly used screening method, but it has the limitations of insufficient specificity. There is an urgent need for molecular markers to assist diagnosis.

methodsA total of 240 patients with pulmonary nodules were enrolled in this study. The expression of serum miR-760 was detected by polymerase chain reaction (PCR). Receiver operating curve (ROC) was used to evaluate the potential of miR-760 in the diagnosis of lung cancer, and logistic regression analysis was used to evaluate its significance in the risk assessment of lung cancer. Target genes were screened by bioinformatics, protein-protein interaction (PPI) network was constructed, and hub genes were screened.

resultsThe expression of miR-760 in the lung cancer group was significantly lower than that in the benign group (P < 0.001). Its AUC for differentiating benign and malignant was 0.867. When LDCT combined with miR-760, the area under the curve (AUC) increased to 0.955. Logistic regression analysis showed that miR-760 was a risk factor for lung cancer incidence. PPI network analysis screened 10 hub genes (HMGCR, INSR, CDK6, etc.), which were enriched in cancer related pathways such as HIF-1 and actin cytoskeleton.

conclusionsmiR-760 combined with LDCT can significantly improve the differentiation ability of benign and malignant pulmonary nodules, and its mechanism may activate tumor-related signaling pathways by targeting the core genes of PPI network. This study provides a new combination of molecular markers and mechanistic clues for the accurate diagnosis of pulmonary nodules.

Indexed as

Lung NeoplasmsMicroRNAsSolitary Pulmonary NoduleTomography, Spiral ComputedAgedArea Under CurveDiagnosis, DifferentialFemaleGene Expression Regulation, NeoplasticHumansLogistic ModelsMaleMiddle AgedProtein Interaction MapsROC CurveMicroRNAsMIRN760 microRNA, humanDiagnostic biomarkerLow-dose spiral CTMiR-760Pulmonary nodules

Identifiers

PMID42104044
PMCPMC13337837

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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.