Metabolomics Platform, Faculty of Biology and Medicine , University of Lausanne , CH-1005 Lausanne , Switzerland.
Department of Molecular Medicine and Surgery , Karolinska Institute , 171 77 Stockholm , Sweden.
Anal Chem. 2018 Jul 17;90(14):8396-8403. doi: 10.1021/acs.analchem.8b00875. Epub 2018 Jun 28.
Comprehensive metabolomic data can be achieved using multiple orthogonal separation and mass spectrometry (MS) analytical techniques. However, drawing biologically relevant conclusions from this data and combining it with additional layers of information collected by other omic technologies present a significant bioinformatic challenge. To address this, a data processing approach was designed to automate the comprehensive prediction of dysregulated metabolic pathways/networks from multiple data sources. The platform autonomously integrates multiple MS-based metabolomics data types without constraints due to different sample preparation/extraction, chromatographic separation, or MS detection method. This multimodal analysis streamlines the extraction of biological information from the metabolomics data as well as the contextualization within proteomics and transcriptomics data sets. As a proof of concept, this multimodal analysis approach was applied to a colorectal cancer (CRC) study, in which complementary liquid chromatography-mass spectrometry (LC-MS) data were combined with proteomic and transcriptomic data. Our approach provided a highly resolved overview of colon cancer metabolic dysregulation, with an average 17% increase of detected dysregulated metabolites per pathway and an increase in metabolic pathway prediction confidence. Moreover, 95% of the altered metabolic pathways matched with the dysregulated genes and proteins, providing additional validation at a systems level. The analysis platform is currently available via the XCMS Online ( XCMSOnline.scripps.edu ).
综合代谢组学数据可以通过多种正交分离和质谱(MS)分析技术来实现。然而,从这些数据中得出具有生物学相关性的结论,并将其与其他组学技术收集的额外信息层相结合,这是一个重大的生物信息学挑战。为了解决这个问题,我们设计了一种数据处理方法,以自动从多个数据源综合预测失调的代谢途径/网络。该平台自主整合了多种基于 MS 的代谢组学数据类型,不受不同样品制备/提取、色谱分离或 MS 检测方法的限制。这种多模态分析简化了从代谢组学数据中提取生物学信息的过程,以及在蛋白质组学和转录组学数据集中进行上下文分析的过程。作为概念验证,我们将这种多模态分析方法应用于结直肠癌(CRC)研究,其中互补的液相色谱-质谱(LC-MS)数据与蛋白质组学和转录组学数据相结合。我们的方法提供了结直肠癌代谢失调的高度解析概述,每个途径检测到的失调代谢物平均增加了 17%,代谢途径预测的置信度也有所提高。此外,95%的改变代谢途径与失调基因和蛋白质相匹配,在系统水平上提供了额外的验证。该分析平台目前可通过 XCMS Online(XCMSOnline.scripps.edu)获取。