Evaluation of human neutrophil peptide-1, -2 and -3 as serum markers for colorectal cancer

  • Irene Van Den Broek*
  • , Rolf W. Sparidans
  • , Judith Y M N Engwegen
  • , Annemieke Cats
  • , Annekatrien C T M Depla
  • , Jan H M Schellens
  • , Jos H. Beijnen
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Increased total serum concentrations of human neutrophil peptide-1, -2 and -3 (HNP-1, -2 and -3) have been associated with colorectal cancer (CRC). Owing to a recently developed and fully validated liquid-chromatography coupled to tandem-mass spectrometry (LC-MS/MS) assay, individual serum concentrations of these antimicrobial peptides were quantified to evaluate their role as serum markers in CRC. Serum was obtained from patients with indications for colonoscopy, subsequently diagnosed as normal colon or hyperplastic polyp (CON; n = 368), adenomatous polyp (AP; n = 179) or colorectal cancer (CRC; n = 69). Comparison of HNP-1, -2 and -3 concentrations between CRC and CON (130 ± 90 vs. 105 ± 80; 264 ± 140 vs. 206 ± 99 and 62 ± 56 vs. 54 ± 59 for HNP-1, -2 and -3, respectively) revealed that reported up-regulated total HNP-concentrations can be largely attributed to increased HNP-2 (P = 0.0006) and HNP-1 (P = 0.024) levels. Although receiver operating characteristics (ROC) analyses showed low specificity of the peptides for CRC and no significant changes in serum levels were observed after surgical removal of the tumor (n = 23), the established differentiation between the HNP-subtypes may be particularly useful to completely elucidate the role of these antimicrobial peptides in CRC.

Original languageEnglish
Pages (from-to)109-115
Number of pages7
JournalCancer Biomarkers
Volume7
Issue number2
DOIs
Publication statusPublished - 2010

Keywords

  • colorectal cancer
  • Human neutrophil peptides
  • LC-MS/MS
  • serum markers

Fingerprint

Dive into the research topics of 'Evaluation of human neutrophil peptide-1, -2 and -3 as serum markers for colorectal cancer'. Together they form a unique fingerprint.

Cite this