代谢组学
癌症
气相色谱-质谱法
质谱法
癌症生物标志物
色谱法
尿
化学
医学
计算生物学
内科学
生物
作者
Yue Liu,Dianlong Ge,Jijuan Zhou,Xiangxue Zheng,Yajing Chu,Yuzhou Yu,Wenting Liu,Ke Li,Yan Lü,Chaoqun Huang,Chengyin Shen,Yannan Chu,Yannan Chu,Yannan Chu
标识
DOI:10.1021/acs.jproteome.5c00255
摘要
Early cancer detection is crucial for improving cure and survival rates. Pan-cancer detection technology enables simultaneous screening for multiple cancer types, representing a significant advancement in cancer diagnosis. Recent biomedical research suggests that cancer may function as a metabolic disorder, underscoring the importance of multiomics, particularly metabolomics. Volatile organic compounds (VOCs) in metabolomics provide noninvasive methods for early disease screening. However, a reliable strategy for VOC analysis in early pan-cancer detection is currently lacking. In this study, we established a N-Nitrosodiethylamine (DEN)-ethanol induction pan-cancer mouse model to longitudinally monitor metabolomic samples (urine, feces, and odor) for VOCs throughout the entire tumor growth process. We employed headspace solid-phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) technology for untargeted tracking and profiling of tumor growth. Through statistical analysis, we identified characteristic metabolites from different metabolomic samples and determined their corresponding early screening time points. These VOCs demonstrated excellent performance in distinguishing tumor development and assessing differences between tumor and healthy groups in validation analyses. This study emphasizes the potential of VOCs in noninvasive whole cancer screening and early diagnosis, providing a fundamental reference for VOCs based gas biopsy experiments in preclinical stages, and demonstrating the concept of early tumor detection.
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