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利用靶向血清代谢谱分析检测结直肠癌

Colorectal cancer detection using targeted serum metabolic profiling.

作者信息

Zhu Jiangjiang, Djukovic Danijel, Deng Lingli, Gu Haiwei, Himmati Farhan, Chiorean E Gabriela, Raftery Daniel

机构信息

Northwest Metabolomics Research Center, Department of Anesthesiology and Pain Medicine, University of Washington , 850 Republican Street, Seattle, Washington 98109, United States.

出版信息

J Proteome Res. 2014 Sep 5;13(9):4120-30. doi: 10.1021/pr500494u. Epub 2014 Aug 15.

Abstract

Colorectal cancer (CRC) is one of the most prevalent and deadly cancers in the world. Despite an expanding knowledge of its molecular pathogenesis during the past two decades, robust biomarkers to enable screening, surveillance, and therapy monitoring of CRC are still lacking. In this study, we present a targeted liquid chromatography-tandem mass spectrometry-based metabolic profiling approach for identifying biomarker candidates that could enable highly sensitive and specific CRC detection using human serum samples. In this targeted approach, 158 metabolites from 25 metabolic pathways of potential significance were monitored in 234 serum samples from three groups of patients (66 CRC patients, 76 polyp patients, and 92 healthy controls). Partial least-squares-discriminant analysis (PLS-DA) models were established, which proved to be powerful for distinguishing CRC patients from both healthy controls and polyp patients. Receiver operating characteristic curves generated based on these PLS-DA models showed high sensitivities (0.96 and 0.89, respectively, for differentiating CRC patients from healthy controls or polyp patients), good specificities (0.80 and 0.88), and excellent areas under the curve (0.93 and 0.95). Monte Carlo cross validation was also applied, demonstrating the robust diagnostic power of this metabolic profiling approach.

摘要

结直肠癌(CRC)是全球最常见且致命的癌症之一。尽管在过去二十年中对其分子发病机制的认识不断扩展,但仍缺乏能够用于结直肠癌筛查、监测和治疗监测的可靠生物标志物。在本研究中,我们提出了一种基于靶向液相色谱 - 串联质谱的代谢谱分析方法,用于鉴定生物标志物候选物,该方法能够使用人血清样本实现对结直肠癌的高度灵敏和特异检测。在这种靶向方法中,对来自三组患者(66例结直肠癌患者、76例息肉患者和92例健康对照)的234份血清样本中25条具有潜在重要性的代谢途径中的158种代谢物进行了监测。建立了偏最小二乘判别分析(PLS - DA)模型,该模型在区分结直肠癌患者与健康对照及息肉患者方面表现强大。基于这些PLS - DA模型生成的受试者工作特征曲线显示出高灵敏度(分别为0.96和0.89,用于区分结直肠癌患者与健康对照或息肉患者)、良好的特异性(0.80和0.88)以及出色的曲线下面积(0.93和0.95)。还应用了蒙特卡洛交叉验证,证明了这种代谢谱分析方法具有强大的诊断能力。

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