利用基于核磁共振的代谢组学进行癌症诊断。

K Odunsi
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引用次数: 9

摘要

对于一些实体人类恶性肿瘤,目前可用的血清生物标志物不足以可靠地区分患者和健康个体。代谢组学是研究生物系统中代谢过程的一门学科,它基于使用1H-NMR光谱和多元统计来生成和解释生化数据,并可能提供疾病的特征指纹。在这里,我们回顾了我们利用代谢组学方法区分上皮性卵巢癌(EOC)妇女血清与健康对照的初步经验。对38例EOC患者、12例良性卵巢囊肿患者和53例健康女性术前血清标本进行1H-NMR分析。PCA分析使38例EOC患者(100%)的所有血清标本与所有21例绝经前正常标本(100%)和所有良性卵巢疾病患者(100%)的血清标本正确分离。此外,38例(97.4%)癌症标本中有37例(97.4%)与32例(97%)绝经后对照血清中有31例(97%)可以正确分离。ROC分析表明,在h - nmr区域(起始点2.77 ppm和2.04 ppm),有病和无病患者的血清均能以100%的灵敏度和特异性进行鉴定(ROC曲线AUC = 1.0)。这些发现表明,作为早期发现EOC的潜在新策略,1H-NMR代谢组学方法值得进一步评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cancer diagnostics using 1H-NMR-based metabonomics.

For several solid human malignancies, currently available serum biomarkers are insufficiently reliable to distinguish patients from healthy individuals. Metabonomics, the study of metabolic processes in biologic systems, is based on the use of 1H-NMR spectroscopy and multivariate statistics for biochemical data generation and interpretation and may provide a characteristic fingerprint in disease. Here we review our initial experiences utilizing the metabonomic approach for discriminating sera from women with epithelial ovarian cancer (EOC) from healthy controls. 1H-NMR spectroscopic analysis was performed on preoperative serum specimens of 38 EOC patients, 12 patients with benign ovarian cysts and 53 healthy women. PCA analysis allowed correct separation of all serum specimens from 38 patients with EOC (100%) from all of the 21 premenopausal normal samples (100%) and from all the sera from patients with benign ovarian disease (100%). In addition, it was possible to correctly separate 37 of 38 (97.4%) cancer specimens from 31 of 32 (97%) postmenopausal control sera. ROC analysis indicated that the sera from patients with and without disease could be identified with 100% sensitivity and specificity at the 1H-NMR regions 2.77 parts per million (ppm) and 2.04 ppm from the origin (AUC of ROC curve = 1.0). These findings indicate that the 1H-NMR metabonomic approach deserves further evaluation as a potential novel strategy for the early detection of EOC.

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