Serum phosphopeptide profiling for colorectal cancer diagnosis using liquid chromatography-mass spectrometry

被引:2
作者
Zhai, Guijin [1 ,2 ,3 ,4 ,5 ]
Yang, Liping [6 ]
Luo, Qun [1 ,2 ,3 ,7 ]
Wu, Kui [1 ,2 ,3 ]
Zhao, Yao [1 ,2 ,3 ]
Wang, Fuyi [1 ,2 ,3 ,7 ,8 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Ctr Mass Spectrometry Beijing, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, CAS Key Lab Analyt Chem Living Biosyst, Inst Chem, Beijing 100190, Peoples R China
[4] Tianjin Med Univ, Dept Biochem & Mol Biol, Tianjin, Peoples R China
[5] Tianjin Med Univ, Tianjin Key Lab Med Epigenet, Tianjin, Peoples R China
[6] Nantong Univ, Canc Res Ctr, Tumour Hosp, Nantong, Jiangsu, Peoples R China
[7] Univ Chinese Acad Sci, Beijing, Peoples R China
[8] Shandong Univ Tradit Chinese Med, Coll Tradit Chinese Med, Jinan, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
AMINOPEPTIDASE N ACTIVITY; LUNG-CANCER; BIOMARKER; ENRICHMENT; PROTEIN; PEPTIDOME; STATISTICS; CHINA;
D O I
10.1002/rcm.9316
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Rationale The identification and evaluation of novel biomarkers are essential to clinical diagnosis and prognosis of colorectal cancer (CRC). Serum phosphopeptides have been recognized as a potential signature pool for cancers; therefore, we aim to profile the expression of serum phosphopeptides and to evaluate their feasibility in CRC diagnosis. Methods We conducted the characterization and absolute quantification of endogenous phosphopeptides in sera using liquid chromatography-mass spectrometry analysis in combination with enrichment of phosphopeptides by ZrAs-Fe3O4@SiO(2)nanoparticles and use of deuterium-labeled standards. Differentially expressed analysis of four phosphopeptides was performed, generating a two-phosphopeptide-based biomarker, LF3-4, by logistic regression analysis, where LF3-4 is equal to (5.85 - 5.13 x [F3] - 3.57 x [F4]), and [F3] and [F4] are the concentration of phosphopeptides DpSGEGDFLAEGGGVR and ADpSGEGDFLAEGGGVR in sera, respectively. Results The LF3-4 values showed significant difference in CRC cases compared with controls, and yielded a specificity of 100%, leading to correct classification of 56 (93%) out of 60 CRC patients, including 12 (92.3%) of 13 CRC cases in stage I. Double-blind validation showed that 97.5% of CRC cases were discriminated accurately. Conclusions The LF3-4 value was firstly verified to be a potential biomarker for CRC diagnosis, and may expand our view in underlying mechanisms for CRC.
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页数:8
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