肺癌
代谢组学
鉴别诊断
医学
病理
呼出气冷凝液
癌症
生物标志物
肺
气体分析呼吸
代谢物
内科学
接收机工作特性
呼吸道疾病
腺癌
放射免疫分析
新陈代谢
诊断生物标志物
入射(几何)
肿瘤科
肿瘤进展
下调和上调
代谢途径
曲线下面积
免疫组织化学
细胞
化学
胃肠病学
发病机制
癌症研究
代谢组
生物
作者
D. Li,Shuting Yang,Ling Zhang,Lingling Dong,Yueeryeti Sailai,Limin Yao,Chengyu Jin,Xuemei Wei
标识
DOI:10.1177/15330338261470635
摘要
IntroductionLung cancer is a malignant tumor with high global incidence and mortality. Early screening and diagnosis can substantially extend patient survival, yet achieving this remains a challenging objective.MethodsWe collected tissue and plasma samples from patients with benign pulmonary nodules and non-small cell lung cancer (NSCLC). Exhaled breath condensate (EBC) samples were obtained from these patients using a breath condenser. Differential metabolites were identified in samples from 22 NSCLC patients and 20 benign controls by means of ultra-performance liquid chromatography-high resolution mass spectrometry-based untargeted metabolomics.ResultsSeveral differential metabolites overlapped between plasma and tissue samples. Further analysis indicated that the differential metabolites from all three sample types participated in central carbon metabolism in cancer, protein digestion and absorption, and aminoacyl-tRNA biosynthesis. ROC curve analysis of plasma and tissue metabolites showed that each of the top 10 upregulated and downregulated metabolites yielded AUC values greater than 0.8. In EBC, only 29 differential metabolites were detected. Among these, lysine, acetildenafil, and 1-(cyclohexylmethyl) proline may be involved in the progression of NSCLC.ConclusionThis study identified distinctive metabolic markers in plasma, tissue, and EBC from NSCLC patients. However, the purpose of this observational study was merely exploratory, rather than to use these differential metabolites as a diagnostic test for non-small cell lung cancer.
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