Identification of Novel Low Molecular Weight Serum Peptidome Biomarkers for Non-Small Cell Lung Cancer (NSCLC)

被引:20
作者
Yang, Juan [1 ]
Song, Yong-Chun [2 ]
Song, Tu-Sheng [1 ]
Hu, Xiao-Yan [1 ]
Guo, You-Min [3 ]
Li, Zong-Fang [4 ]
Dang, Cheng-Xue [2 ]
Huang, Chen [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Med, Dept Genet & Mol Biol, Key Lab Environm & Dis Related Gene,Minist Educ, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Coll Med, Affiliated Hosp 1, Dept Tumor Surg, Xian 710061, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Med Image, Xian 710061, Shaanxi, Peoples R China
[4] Xi An Jiao Tong Univ, Dept Resp Med, Affiliated Hosp 2, Key Lab Environm & Genes Related Dis,Minist Educ, Xian 710061, Shaanxi, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
MALDI-TOF MS; NSCLC; COPD; pneumonia; magnetic beads; serum biomarkers; DIAGNOSIS; SPECTROMETRY; DISCOVERY;
D O I
10.1002/jcla.21502
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Aim To identify discriminating protein patterns in serum samples among non-small cell lung cancer (NSCLC), chronic obstructive pulmonary disease (COPD), pneumonia, and healthy controls. To discover specific low molecular weight (LMW) serum peptidome biomarkers and establish a diagnostic pattern for NSCLCby using proteomic technology. Methods We used magnetic bead-based separation followed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) to identify patients with NSCLC, COPD, and pneumonia. A total of 154 serum samples were analyzed in this study, among which there were 60 serum samples from NSCLC patients, 30 from patients with other lung-related diseases (16 pneumonia patients and 14 patients with COPD) as disease controls, and 64 from healthy volunteers as healthy control. The mass spectra, analyzed using ClinProTools software, distinguished between cancer patients and healthy individuals based on GA algorithm model. Results In this study, we generated numerous discriminating m/z peaks as well as disease-specific discrimination peaks. A set of five potential biomarkers (m/z: 7,763.24, 1,012.61, 4,153.16, 1,450.55, and 2,878.89) could be used as the diagnostic biomarkers to distinguish NSCLCpatients from healthy controls. In the training set, patients with NSCLC could be identified with sensitivity of 97.5% and specificity of 98.8%. Similar results were obtained in the testing set, showing 80.7% sensitivity and 91.2% specificity. Conclusion Our study demonstrated that a combined application of magnetic beads with MALDI-TOF MS technique was suitable for identification of serum biomarkers for NSCLC. J. Clin. Lab. Anal. 26:148-154, 2012. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:148 / 154
页数:7
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