Abaffy T, Möller M G, Riemer D D, Milikowski C, DeFazio R A
Molecular and Cellular Pharmacology, University of Miami, Miami, FL USA.
Division of Surgical Oncology, DeWitt Daughtry Department of Surgery, University of Miami, Miami, FL USA.
Metabolomics. 2013;9(5):998-1008. doi: 10.1007/s11306-013-0523-z. Epub 2013 Mar 30.
The analysis of volatile organic compounds (VOC) as biomarkers of cancer is both promising and challenging. In this pilot study, we used an untargeted approach to compare volatile metabolomic signatures of melanoma and matched control non-neoplastic skin from the same patient. VOC from fresh (non-fixed) biopsied tissue were collected using the headspace solid phase micro extraction method (HS SPME) and analyzed by gas chromatography and mass spectrometry (GCMS). We applied the XCMS analysis platform and MetaboAnalyst software to reveal many differentially expressed metabolic features. Our analysis revealed increased levels of lauric acid (C12:0) and palmitic acid (C16:0) in melanoma. The identity of these compounds was confirmed by comparison with chemical standards. Increased levels of these fatty acids are likely to be a consequence of up-regulated de novo lipid synthesis, a known characteristic of cancer. Increased oxidative stress is likely to cause an additional increase in lauric acid. Implementation of this study design on larger number of cases will be necessary for the future metabolomics biomarker discovery applications.
将挥发性有机化合物(VOC)作为癌症生物标志物进行分析既充满前景又具有挑战性。在这项初步研究中,我们采用非靶向方法比较了同一患者黑色素瘤与匹配的对照非肿瘤性皮肤的挥发性代谢组学特征。使用顶空固相微萃取法(HS SPME)收集新鲜(非固定)活检组织中的VOC,并通过气相色谱和质谱(GCMS)进行分析。我们应用XCMS分析平台和MetaboAnalyst软件来揭示许多差异表达的代谢特征。我们的分析显示,黑色素瘤中月桂酸(C12:0)和棕榈酸(C16:0)水平升高。通过与化学标准品比较,证实了这些化合物的身份。这些脂肪酸水平的升高可能是由于从头脂质合成上调所致,这是癌症的一个已知特征。氧化应激增加可能会导致月桂酸进一步增加。为了未来的代谢组学生物标志物发现应用,有必要对更多病例实施本研究设计。