Discovery of novel bladder cancer biomarkers by comparative urine proteomics using iTRAQ technology

Yi Ting Chen*, Chien Lun Chen, Hsiao Wei Chen, Ting Chung, Chih Ching Wu, Chi De Chen, Chia Wei Hsu, Meng Chieh Chen, Ke Hung Tsui, Phei Lang Chang, Yu Sun Chang, Jau Song Yu

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

137 Scopus citations

Abstract

A urine sample preparation workflow for the iTRAQ (isobaric tag for relative and absolute quantitation) technique was established. The reproducibility of this platform was evaluated and applied to discover proteins with differential levels between pooled urine samples from nontumor controls and three bladder cancer patient subgroups with different grades/stages (a total of 14 controls and 23 cancer cases in two multiplex iTRAQ runs). Combining the results of two independent clinical sample sets, a total of 638 urine proteins were identified. Among them, 55 proteins consistently showed >2-fold differences in both sample sets. Western blot analyses of individual urine samples confirmed that the levels of apolipoprotein A-I (APOA1), apolipoprotein A-II, heparin cofactor 2 precursor and peroxiredoxin-2 were significantly elevated in bladder cancer urine specimens (n = 25-74). Finally, we quantified APOA1 in a number of urine samples using a commercial ELISA and confirmed again its potential value for diagnosis (n = 126, 94.6% sensitivity and 92.0% specificity at a cutoff value of 11.16 ng/mL) and early detection (n = 71, 83.8% sensitivity and 94.0% specificity). Collectively, our results provide the first iTRAQ-based quantitative profile of bladder cancer urine proteins and represent a valuable resource for the discovery of bladder cancer markers.

Original languageEnglish
Pages (from-to)5803-5815
Number of pages13
JournalJournal of Proteome Research
Volume9
Issue number11
DOIs
StatePublished - 05 11 2010

Keywords

  • apolipoprotein
  • biomarkers
  • bladder cancer
  • heparin cofactor 2 precursor
  • iTRAQ
  • peroxiredoxin-2
  • urine proteome

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