代谢组学
化学
代谢途径
低牛磺酸
小桶
代谢组
代谢网络
生物标志物发现
色谱法
计算生物学
新陈代谢
蛋白质组学
牛磺酸
生物化学
氨基酸
转录组
生物
基因
基因表达
作者
Aihua Zhang,Hui Sun,Ying Han,Guangli Yan,Ye Yuan,Gaochen Song,Xiaoxia Yuan,Ning Xie,Xijun Wang
摘要
Metabolomics is the study of metabolic changes in biological systems and provides the small molecule fingerprints related to the disease. Extracting biomedical information from large metabolomics data sets by multivariate data analysis is of considerable complexity. Therefore, more efficient and optimizing metabolomics data processing technologies are needed to improve mass spectrometry applications in biomarker discovery. Here, we report the findings of urine metabolomic investigation of hepatitis C virus (HCV) patients by high-throughput ultraperformance liquid chromatography–mass spectrometry (UPLC–MS) coupled with pattern recognition methods (principal component analysis, partial least-squares, and OPLS-DA) and network pharmacology. A total of 20 urinary differential metabolites (13 upregulated and 7 downregulated) were identified and contributed to HCV progress, involve several key metabolic pathways such as taurine and hypotaurine metabolism, glycine, serine and threonine metabolism, histidine metabolism, arginine and proline metabolism, and so forth. Metabolites identified through metabolic profiling may facilitate the development of more accurate marker algorithms to better monitor disease progression. Network analysis validated close contact between these metabolites and implied the importance of the metabolic pathways. Mapping altered metabolites to KEGG pathways identified alterations in a variety of biological processes mediated through complex networks. These findings may be promising to yield a valuable and noninvasive tool that insights into the pathophysiology of HCV and to advance the early diagnosis and monitor the progression of disease. Overall, this investigation illustrates the power of the UPLC–MS platform combined with the pattern recognition and network analysis methods that can engender new insights into HCV pathobiology.
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