Metabolomic investigation of urinary extracellular vesicles for early detection and screening of lung cancer

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作者
Qinsi Yang
Jiaxin Luo
Hao Xu
Liu Huang
Xinxi Zhu
Hengrui Li
Rui Yang
Bo Peng
Da Sun
Qingfu Zhu
Fei Liu
机构
[1] University of Chinese Academy of Sciences,Wenzhou Institute
[2] Wenzhou Medical University,National Engineering Research Center of Ophthalmology and Optometry, Eye Hospital
[3] Huazhong University of Science and Technology,Department of Oncology, Tongji Hospital, Tongji Medical College
[4] The First Affiliated Hospital of Wenzhou Medical University,Key Laboratory of Heart and Lung
[5] Wenzhou University,Institute of Life Sciences & Engineering Laboratory of Zhejiang Province for Pharmaceutical Development of Growth Factors
[6] The First Affiliated Hospital of Wenzhou Medical University,undefined
关键词
Lung cancer; Metabolomics; Extracellular vesicles; Early diagnosis;
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摘要
Lung cancer is a prevalent cancer type worldwide that often remains asymptomatic in its early stages and is frequently diagnosed at an advanced stage with a poor prognosis due to the lack of effective diagnostic techniques and molecular biomarkers. However, emerging evidence suggests that extracellular vesicles (EVs) may promote lung cancer cell proliferation and metastasis, and modulate the anti-tumor immune response in lung cancer carcinogenesis, making them potential biomarkers for early cancer detection. To investigate the potential of urinary EVs for non-invasive detection and screening of patients at early stages, we studied metabolomic signatures of lung cancer. Specifically, we conducted metabolomic analysis of 102 EV samples and identified metabolome profiles of urinary EVs, including organic acids and derivatives, lipids and lipid-like molecules, organheterocyclic compounds, and benzenoids. Using machine learning with a random forest model, we screened for potential markers of lung cancer and identified a marker panel consisting of Kanzonol Z, Xanthosine, Nervonyl carnitine, and 3,4-Dihydroxybenzaldehyde, which exhibited a diagnostic potency of 96% for the testing cohort (AUC value). Importantly, this marker panel also demonstrated effective prediction for the validation set, with an AUC value of 84%, indicating the reliability of the marker screening process. Our findings suggest that the metabolomic analysis of urinary EVs provides a promising source of non-invasive markers for lung cancer diagnostics. We believe that the EV metabolic signatures could be used to develop clinical applications for the early detection and screening of lung cancer, potentially improving patient outcomes.
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