Lu Xiaojie, Ji Li-Juan, Chen Jin-Lian
Department of Gastroenterology, Shanghai East Hospital, Tongji University, School of Medicine, Shanghai, China.
Department of Rehabilitation, The Second People's Hospital of Huai'an, Huai'an, China.
Methods Enzymol. 2014;543:261-73. doi: 10.1016/B978-0-12-801329-8.00013-1.
Most cancers develop upon the accumulation of genetic alterations that provoke and sustain the transformed phenotype. Several metabolomic approaches now allow for the global assessment of intermediate metabolites, generating profound insights into the metabolic rewiring associated with malignant transformation. The metabolomic profiling of neoplastic lesions growing in mice, irrespective of their origin, can provide invaluable information on the mechanisms underlying oncogenesis, tumor progression, and response to therapy. Moreover, the metabolomic profiling of tumors growing in mice may result in the identification of novel diagnostic or prognostic biomarkers, which is of great clinical significance. Several methods can be applied to the metabolomic profiling of neoplastic lesions in mice, including mass spectrometry-based techniques (e.g., gas chromatography-, capillary electrophoresis-, or liquid chromatography-coupled mass spectrometry) as well as nuclear magnetic resonance. Here, we compare and discuss the advantages and disadvantages of all these techniques to provide a concise and reliable guide for readers interested in this active area of investigation.
大多数癌症是在引发并维持转化表型的基因改变积累后发生的。目前,几种代谢组学方法能够对中间代谢产物进行全面评估,从而深入了解与恶性转化相关的代谢重编程。对小鼠体内生长的肿瘤性病变进行代谢组学分析,无论其起源如何,都能为肿瘤发生、肿瘤进展及治疗反应的潜在机制提供宝贵信息。此外,对小鼠体内生长的肿瘤进行代谢组学分析可能会鉴定出新的诊断或预后生物标志物,这具有重大临床意义。有几种方法可用于小鼠肿瘤性病变的代谢组学分析,包括基于质谱的技术(如气相色谱 - 、毛细管电泳 - 或液相色谱 - 联用质谱)以及核磁共振。在此,我们比较并讨论所有这些技术的优缺点,为对这一活跃研究领域感兴趣的读者提供一份简洁可靠的指南。