CICECO, Department of Chemistry, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.
J Proteome Res. 2011 Jan 7;10(1):221-30. doi: 10.1021/pr100899x. Epub 2010 Nov 23.
In this study, ¹H NMR-based metabonomics has been applied, for the first time to our knowledge, to investigate lung cancer metabolic signatures in urine, aiming at assessing the diagnostic potential of this approach and gaining novel insights into lung cancer metabolism and systemic effects. Urine samples from lung cancer patients (n = 71) and a control healthy group (n = 54) were analyzed by high resolution ¹H NMR (500 MHz), and their spectral profiles subjected to multivariate statistics, namely, Principal Component Analysis (PCA), Partial Least Squares Discriminant Analysis (PLS-DA), and Orthogonal Projections to Latent Structures (OPLS)-DA. Very good discrimination between cancer and control groups was achieved by multivariate modeling of urinary profiles. By Monte Carlo Cross Validation, the classification model showed 93% sensitivity, 94% specificity and an overall classification rate of 93.5%. The possible confounding influence of other factors, namely, gender and age, have also been modeled and found to have much lower predictive power than the presence of the disease. Moreover, smoking habits were found not to have a dominating influence over class discrimination. The main metabolites contributing to this discrimination, as highlighted by multivariate analysis and confirmed by spectral integration, were hippurate and trigonelline (reduced in patients), and β-hydroxyisovalerate, α-hydroxyisobutyrate, N-acetylglutamine, and creatinine (elevated in patients relatively to controls). These results show the valuable potential of NMR-based metabonomics for finding putative biomarkers of lung cancer in urine, collected in a minimally invasive way, which may have important diagnostic impact, provided that these metabolites are found to be specifically disease-related.
在这项研究中,¹H NMR 代谢组学首次被应用于尿液中的肺癌代谢特征研究,旨在评估该方法的诊断潜力,并深入了解肺癌代谢和全身效应。对 71 例肺癌患者和 54 例健康对照组的尿液样本进行了高分辨率¹H NMR(500 MHz)分析,并对其光谱谱图进行了多元统计分析,即主成分分析(PCA)、偏最小二乘判别分析(PLS-DA)和正交偏最小二乘判别分析(OPLS-DA)。通过对尿液谱的多元建模,实现了癌症组和对照组之间的良好区分。通过蒙特卡罗交叉验证,分类模型的灵敏度为 93%,特异性为 94%,总分类率为 93.5%。还对性别和年龄等其他因素的可能混杂影响进行了建模,发现其预测能力远低于疾病的存在。此外,吸烟习惯对分类判别没有主导影响。多变量分析和光谱积分均证实,对这种区分有贡献的主要代谢物是马尿酸和瓜氨酸(患者中减少),以及β-羟基异戊酸、α-羟基异丁酸、N-乙酰谷氨酸和肌酐(与对照组相比患者中升高)。这些结果表明,基于 NMR 的代谢组学在寻找非侵入性尿液中肺癌潜在生物标志物方面具有有价值的潜力,这些标志物可能具有重要的诊断影响,前提是这些代谢物被发现与疾病有特异性关系。