4.8 Article

Sequential Orbitrap Secondary Ion Mass Spectrometry and Liquid Extraction Surface Analysis-Tandem Mass Spectrometry-Based Metabolomics for Prediction of Brain Tumor Relapse from Sample-Limited Primary Tissue Archives

期刊

ANALYTICAL CHEMISTRY
卷 93, 期 18, 页码 6947-6954

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.0c05087

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资金

  1. Engineering and Physical Sciences Research Council [EP/N006615/1]
  2. EPSRC Programme Grant for Next Generation Biomaterials Discovery
  3. EPSRC [EP/N006615/1] Funding Source: UKRI

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A novel surface mass spectrometry strategy was used to perform untargeted metabolite profiling of pediatric ependymoma samples, detecting 887 metabolites and identifying key metabolites and pathways predictive of tumor relapse through data fusion and multivariate analysis. This sequential mass spectrometry strategy has proven to be a versatile tool for high-throughput metabolite profiling on sample-limited tissue archives.
We present here a novel surface mass spectrometry strategy to perform untargeted metabolite profiling of formalin-fixed paraffin-embedded pediatric ependymoma archives. Sequential Orbitrap secondary ion mass spectrometry (3D OrbiSIMS) and liquid extraction surface analysis-tandem mass spectrometry (LESA-MS/MS) permitted the detection of 887 metabolites (163 chemical classes) from pediatric ependymoma tumor tissue microarrays (diameter: <1 mm; thickness: 4 mu m). From these 163 classes, 60 classes were detected with both techniques, whilst LESA-MS/MS and 3D OrbiSIMS individually allowed the detection of another 83 and 20 unique metabolite classes, respectively. Through data fusion and multivariate analysis, we were able to identify key metabolites and corresponding pathways predictive of tumor relapse, which were retrospectively confirmed by gene expression analysis with publicly available data. Altogether, this sequential mass spectrometry strategy has shown to be a versatile tool to perform high-throughput metabolite profiling on sample-limited tissue archives.

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