Plasma exosomal tsRNA may be used as a marker for differential diagnosis of benign and malignant pulmonary nodules

Abstract Background tRNA-derived small RNAs (tsRNAs) have garnered significant attention in the field of cancer research, however, exosomal tsRNAs remain relatively understudied as potential biomarkers in the pulmonary nodules. This study aims to identify exosomal tsRNAs that are differentially expr...

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Main Authors: Na Zhou, Kecheng Li, Li Xie
Format: Article
Language:English
Published: BMC 2025-07-01
Series:Journal of Translational Medicine
Subjects:
Online Access:https://doi.org/10.1186/s12967-025-06737-3
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author Na Zhou
Kecheng Li
Li Xie
author_facet Na Zhou
Kecheng Li
Li Xie
author_sort Na Zhou
collection DOAJ
description Abstract Background tRNA-derived small RNAs (tsRNAs) have garnered significant attention in the field of cancer research, however, exosomal tsRNAs remain relatively understudied as potential biomarkers in the pulmonary nodules. This study aims to identify exosomal tsRNAs that are differentially expressed between benign and malignant pulmonary nodules, integrate these findings with other clinical parameters, and develop a novel predictive model to estimate the likelihood of malignancy in pulmonary nodules. Methods Exosomes were extracted from plasma of patients with benign pulmonary nodules and malignant pulmonary nodules (early-stage lung cancer), then characterized using transmission electron microscopy (TEM), qNano, and western blot. Differentially expressed tsRNAs were identified through small RNA microarray screening and validated by Quantitative Real-Time PCR (qRT-PCR). Receiver operating characteristic (ROC) analysis evaluated their diagnostic efficiency, while logistic regression integrated blood and imaging data to build a predictive model. Diagnostic performance was further assessed using random forest and nomogram analyses. Results A total of 43 differentially expressed tsRNAs were identified through small RNA array analysis. Among these, the expression levels of 3’tiRNA-43-GlyGCC-4 and tRF3-17-GlyTCC were significantly higher in patients with benign pulmonary nodules compared to those with early-stage lung cancer. Conversely, the expression of 5’Leader-ValAAC-1-2 was significantly lower in benign cases than in early-stage lung cancer patients. Using logistic regression, a predictive model was constructed by combining these tsRNA biomarkers with blood-based and imaging parameters. The model demonstrated excellent performance in distinguishing early-stage lung cancer from benign pulmonary nodules, achieving an area under the curve (AUC) of 0.9559, with a sensitivity of 91.06% and a specificity of 91.53%. Conclusion Our model highlights its potential as a robust tool for predicting the malignancy probability of pulmonary nodules.
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spelling doaj-art-265a2a9b9be147f791bacae73f11e36c2025-08-20T03:45:32ZengBMCJournal of Translational Medicine1479-58762025-07-0123111910.1186/s12967-025-06737-3Plasma exosomal tsRNA may be used as a marker for differential diagnosis of benign and malignant pulmonary nodulesNa Zhou0Kecheng Li1Li Xie2Shandong University Cancer CenterMedical Research & Laboratory Diagnostic Center, Central Hospital Affiliated to Shandong First Medical UniversityShandong University Cancer CenterAbstract Background tRNA-derived small RNAs (tsRNAs) have garnered significant attention in the field of cancer research, however, exosomal tsRNAs remain relatively understudied as potential biomarkers in the pulmonary nodules. This study aims to identify exosomal tsRNAs that are differentially expressed between benign and malignant pulmonary nodules, integrate these findings with other clinical parameters, and develop a novel predictive model to estimate the likelihood of malignancy in pulmonary nodules. Methods Exosomes were extracted from plasma of patients with benign pulmonary nodules and malignant pulmonary nodules (early-stage lung cancer), then characterized using transmission electron microscopy (TEM), qNano, and western blot. Differentially expressed tsRNAs were identified through small RNA microarray screening and validated by Quantitative Real-Time PCR (qRT-PCR). Receiver operating characteristic (ROC) analysis evaluated their diagnostic efficiency, while logistic regression integrated blood and imaging data to build a predictive model. Diagnostic performance was further assessed using random forest and nomogram analyses. Results A total of 43 differentially expressed tsRNAs were identified through small RNA array analysis. Among these, the expression levels of 3’tiRNA-43-GlyGCC-4 and tRF3-17-GlyTCC were significantly higher in patients with benign pulmonary nodules compared to those with early-stage lung cancer. Conversely, the expression of 5’Leader-ValAAC-1-2 was significantly lower in benign cases than in early-stage lung cancer patients. Using logistic regression, a predictive model was constructed by combining these tsRNA biomarkers with blood-based and imaging parameters. The model demonstrated excellent performance in distinguishing early-stage lung cancer from benign pulmonary nodules, achieving an area under the curve (AUC) of 0.9559, with a sensitivity of 91.06% and a specificity of 91.53%. Conclusion Our model highlights its potential as a robust tool for predicting the malignancy probability of pulmonary nodules.https://doi.org/10.1186/s12967-025-06737-3tsRNADiagnosisBenignMalignantPulmonary noduleExosome
spellingShingle Na Zhou
Kecheng Li
Li Xie
Plasma exosomal tsRNA may be used as a marker for differential diagnosis of benign and malignant pulmonary nodules
Journal of Translational Medicine
tsRNA
Diagnosis
Benign
Malignant
Pulmonary nodule
Exosome
title Plasma exosomal tsRNA may be used as a marker for differential diagnosis of benign and malignant pulmonary nodules
title_full Plasma exosomal tsRNA may be used as a marker for differential diagnosis of benign and malignant pulmonary nodules
title_fullStr Plasma exosomal tsRNA may be used as a marker for differential diagnosis of benign and malignant pulmonary nodules
title_full_unstemmed Plasma exosomal tsRNA may be used as a marker for differential diagnosis of benign and malignant pulmonary nodules
title_short Plasma exosomal tsRNA may be used as a marker for differential diagnosis of benign and malignant pulmonary nodules
title_sort plasma exosomal tsrna may be used as a marker for differential diagnosis of benign and malignant pulmonary nodules
topic tsRNA
Diagnosis
Benign
Malignant
Pulmonary nodule
Exosome
url https://doi.org/10.1186/s12967-025-06737-3
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AT kechengli plasmaexosomaltsrnamaybeusedasamarkerfordifferentialdiagnosisofbenignandmalignantpulmonarynodules
AT lixie plasmaexosomaltsrnamaybeusedasamarkerfordifferentialdiagnosisofbenignandmalignantpulmonarynodules