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基于生物转化的代谢组学分析方法用于确定和定量与癌症相关的代谢物。

Biotransformation-based metabolomics profiling method for determining and quantitating cancer-related metabolites.

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.

Cancer Institute and Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.

出版信息

J Chromatogr A. 2018 Dec 14;1580:80-89. doi: 10.1016/j.chroma.2018.10.034. Epub 2018 Oct 19.

Abstract

The discovery and identification of reliable disease biomarkers and relevant disrupted metabolic pathways is still a major challenge in metabolomics. Here, we proposed a biotransformation-based metabolomics profiling method to identify reliable disease biomarkers by simultaneous quantitation and qualification of cancer-related metabolites and their metabolic pathways via liquid chromatography-tandem mass spectrometry (LC-MS/MS). The approach was based on selecting a subset of known cancer-related metabolites from our previous metabolomics work, cancer research literature and biological significance. The metabolic profiling of pathway-related metabolites was developed by predicted multiple reaction monitoring (MRM) of ion pairs based on their chemical structures and biotransformation. Then, a high-throughput quantitative method was established. Overall, this approach enables the sensitive and accurate detection of cancer-related metabolites and the identification of other relevant metabolites, which facilitates better data quality and in-depth investigation of dysregulated metabolic pathways. As a proof of concept, the approach was applied to a small-cell lung cancer (SCLC) study. The results showed that 43 metabolites were significantly changed, and arginine metabolism was apparently disturbed, which proved the proposed approach could be a powerful tool for discovering reliable disease biomarkers and aberrant metabolic pathways.

摘要

在代谢组学中,发现和鉴定可靠的疾病生物标志物和相关代谢途径仍然是一个主要挑战。在这里,我们提出了一种基于生物转化的代谢组学分析方法,通过液相色谱-串联质谱(LC-MS/MS)同时定量和定性分析与癌症相关的代谢物及其代谢途径,从而鉴定可靠的疾病生物标志物。该方法基于从我们之前的代谢组学工作、癌症研究文献和生物学意义中选择一组已知的与癌症相关的代谢物。通过基于其化学结构和生物转化的预测多重反应监测(MRM)对离子对进行代谢途径相关代谢物的代谢谱分析。然后,建立了高通量定量方法。总的来说,这种方法能够灵敏准确地检测与癌症相关的代谢物,并鉴定其他相关代谢物,从而提高数据质量并深入研究失调的代谢途径。作为概念验证,该方法应用于小细胞肺癌(SCLC)研究。结果表明,有 43 种代谢物显著改变,精氨酸代谢明显紊乱,这证明了所提出的方法可以成为发现可靠疾病生物标志物和异常代谢途径的有力工具。

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