JG Brown Cancer Center, Department of Chemistry, University of Louisville, Louisville, Kentucky 40202, USA.
OMICS. 2011 Mar;15(3):173-82. doi: 10.1089/omi.2010.0088. Epub 2011 Feb 17.
Metabolomics provides a readout of the state of metabolism in cells or tissue and their responses to external perturbations. For this reason, the approach has great potential in clinical diagnostics. Clinical metabolomics using stable isotope resolved metabolomics (SIRM) for pathway tracing represents an important new approach to obtaining metabolic parameters in human cancer subjects in situ. Here we provide an overview of the technology development of labeling from cells in culture and mouse models. The high throughput analytical methods NMR and mass spectrometry, especially Fourier transform ion cyclotron resonance, for analyzing the resulting metabolite isotopomers and isotopologues are described with examples of applications in cancer biology. Special technical considerations for clinical applications of metabolomics using stable isotope tracers are described. The whole process from concept to analysis will be exemplified by our on-going study of nonsmall cell lung cancer (NSCLC) metabolomics. This powerful new approach has already provided important new insights into metabolic adaptations in lung cancer cells, including the upregulation of anaplerosis via pyruvate carboxylation in NSCLC.
代谢组学提供了细胞或组织代谢状态及其对外界干扰的反应的读数。因此,该方法在临床诊断中有很大的潜力。使用稳定同位素解析代谢组学(SIRM)进行途径追踪的临床代谢组学代表了一种获得原位人类癌症患者代谢参数的重要新方法。在这里,我们提供了细胞培养和小鼠模型中标记技术发展的概述。高吞吐量分析方法 NMR 和质谱法,特别是傅里叶变换离子回旋共振,用于分析所得代谢物同量异位体和同量异位标记物,并举例说明了在癌症生物学中的应用。描述了使用稳定同位素示踪剂进行代谢组学临床应用的特殊技术考虑因素。从概念到分析的整个过程将通过我们正在进行的非小细胞肺癌(NSCLC)代谢组学研究为例。这种强大的新方法已经为肺癌细胞中的代谢适应提供了重要的新见解,包括 NSCLC 中通过丙酮酸羧化作用上调氨酰化。