Identification of fucosylated Fetuin-A as a potential biomarker for cholangiocarcinoma

Lucy Betesh, Mary Ann Comunale, Mengjun Wang, Hongyan Liang, Julie Hafner, Aykan Karabudak, Nasra H. Giama, Catherine D. Moser, Eiji Miyoshi, Lewis R. Roberts, Timothy M. Block, Anand Mehta

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

Purpose: Cholangiocarcinoma (CCA) is a malignancy of the bile ducts. The purpose of this discovery study was to identify effective serum markers for surveillance of cholangiocarcinoma. Experimental design: Using a glycomic method, patients with CCA were determined to have increased levels of alpha-1,3 and alpha-1,6 linked fucosylated glycan. Proteomic analysis of the serum fucosylated proteome identified proteins such as alpha-2-macroglobulin, kininogen, hemopexin, fetuin-A, alpha-1 anti-trypsin, and ceruloplasmin as being hyperfucosylated in HCC. The levels of these glycoproteins in 109 patients with CCA, primary sclerosing cholangitis (PSC), and control patients were compared to the performance of CA-19-9, the current “gold standard” assay for cholangiocarcinoma. Results: Fucosylated Fetuin-A (fc-Fetuin-A) had the best ability to differentiate CCA from PSC, with an AUROC of 0.812 or 0.8665 at differentiating CCA from those with PSC or other liver disease. CA-19-9 had poor ability to differentiate PSC from cholangiocarcinoma (AUROC of 0.625). Conclusion and clinical relevance: Using glycomic and proteomic methods we identified a set of proteins that contain altered glycan in the sera of those with CCA. One of these proteins, fucosylated Fetuin-A may have value in the surveillance of people at risk for the development of cholangiocarcinoma.

Original languageEnglish (US)
Article number1600141
JournalProteomics - Clinical Applications
Volume11
Issue number9-10
DOIs
StatePublished - Sep 2017

Keywords

  • Cholangiocarcinoma
  • Fetuin-A
  • Glycosylation

ASJC Scopus subject areas

  • Clinical Biochemistry

Fingerprint Dive into the research topics of 'Identification of fucosylated Fetuin-A as a potential biomarker for cholangiocarcinoma'. Together they form a unique fingerprint.

  • Cite this

    Betesh, L., Comunale, M. A., Wang, M., Liang, H., Hafner, J., Karabudak, A., Giama, N. H., Moser, C. D., Miyoshi, E., Roberts, L. R., Block, T. M., & Mehta, A. (2017). Identification of fucosylated Fetuin-A as a potential biomarker for cholangiocarcinoma. Proteomics - Clinical Applications, 11(9-10), [1600141]. https://doi.org/10.1002/prca.201600141