Colorectal Cancer Detection Using Targeted Serum Metabolic Profiling

被引:175
作者
Zhu, Jiangjiang [1 ]
Djukovic, Danijel [1 ]
Deng, Lingli [1 ,2 ,3 ]
Gu, Haiwei [1 ]
Himmati, Farhan [1 ]
Chiorean, E. Gabriela [4 ,5 ]
Raftery, Daniel [1 ,6 ]
机构
[1] Univ Washington, Dept Anesthesiol & Pain Med, Northwest Metabol Res Ctr, Seattle, WA 98109 USA
[2] Xiamen Univ, Dept Elect Sci, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Dept Commun Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[4] Univ Washington, Seattle, WA 98109 USA
[5] Indiana Univ, Melvin & Bren Simon Canc Ctr, Indianapolis, IN 46202 USA
[6] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98109 USA
关键词
metabolomics; colorectal cancer; polyps; LC-MS/MS; targeted metabolic profiling; serum metabolites; diagnostic biomarkers; HEPATOCELLULAR-CARCINOMA; AMERICAN-COLLEGE; COLON-CANCER; SURVEILLANCE; METABONOMICS; RESONANCE; MARKERS; GLUCOSE; POLYPS; ACIDS;
D O I
10.1021/pr500494u
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:4120 / 4130
页数:11
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