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Biomarker discovery and identification from non-small cell lung cancer sera

  • Jie Du
  • , Shuan Ying Yang
  • , Xiu Li Lin
  • , Wen Li Shang
  • , Wei Zhang
  • , Shu Fen Huo
  • , Li Na Bu
  • , Bin Zhou
  • , Yan Dong Nan
  • , Hua Dong Zheng
  • , Yan Feng Liu
  • Xi'an Jiaotong University
  • Medical Department of Second Hospital of Xi'an

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

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 nonsmall 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 crossvalidation, 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.

Original languageEnglish
Pages (from-to)1-10
Number of pages10
JournalFrontiers in Bioscience - Elite
Volume3 E
Issue number1
StatePublished - 1 Jan 2011

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Biomarker
  • ClinProt
  • NSCLC
  • Proteomics
  • Sera

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