| Literature DB >> 21196279 |
Jie Du1, Shuan-ying Yang, Xiu-li Lin, Wen-li Shang, Wei Zhang, Shu-fen Huo, Li-na Bu, Wei Zhang, Bin Zhou, Yan-dong Nan, Hua-dong Zheng, Yan-feng Liu.
Abstract
Currently, serum biomarkers might usually be thought not to be used for early detection of lung cancer by some researchers. In this study, we used a highly optimized ClinProt-matrix-assisted laser desorption/ionization time-of flight mass spectrometer (MALDI-TOF-MS) to screen non-small cell lung carcinoma (NSCLC) markers in serum. A training set of spectra derived from 45 NSCLC patients, 24 patients with benign lung diseases (BLDs) and 21 healthy individuals, was used to develop a proteomic pattern that discriminated cancer from non-cancer effectively. A test set, including 74 cases (29 NSCLC patients and 45 controls), was used to validate this pattern. After cross-validation, the classifier showed sensitivity and specificity, 86.20% and 80.00%, respectively. Remarkably, 100% of early stage serum samples could be correctly classified as lung cancer. Furthermore, the differential peptides of 1865Da and 4209Da were identified as element of component 3 and eukaryotic peptide chain release factor GTP-binding subunit ERF, respectively. The patterns we described and peptides we identified may have clinical utility as surrogate markers for detection and classification of NSCLC.Entities:
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Year: 2011 PMID: 21196279 DOI: 10.2741/e214
Source DB: PubMed Journal: Front Biosci (Elite Ed) ISSN: 1945-0494