Application of a Glycoproteomics-Based Biomarker Development Method: Alteration in Glycan Structure on Colony Stimulating Factor 1 Receptor as a Possible Glycobiomarker Candidate for Evaluation of Liver Cirrhosis

The importance of diagnosis and therapies for liver cirrhosis (LC) is indisputable. Thus, a reliable method for monitoring the progression of liver fibrosis and resultant LC is urgently needed. Previously, using a lectin-assisted glycoproteomic method, we identified 26 serum glycoproteins as promisi...

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Published inJournal of proteome research Vol. 13; no. 3; pp. 1428 - 1437
Main Authors Ocho, Makoto, Togayachi, Akira, Iio, Etsuko, Kaji, Hiroyuki, Kuno, Atsushi, Sogabe, Maki, Korenaga, Masaaki, Gotoh, Masanori, Tanaka, Yasuhito, Ikehara, Yuzuru, Mizokami, Masashi, Narimatsu, Hisashi
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 07.03.2014
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Summary:The importance of diagnosis and therapies for liver cirrhosis (LC) is indisputable. Thus, a reliable method for monitoring the progression of liver fibrosis and resultant LC is urgently needed. Previously, using a lectin-assisted glycoproteomic method, we identified 26 serum glycoproteins as promising glycobiomarker candidates for monitoring the progression of liver diseases. In this study, we identified colony stimulating factor 1 receptor (CSF1R) as a promising LC marker candidate and then established Wisteria floribunda agglutinin (WFA)-reactive CSF1R (WFA+-CSF1R) as a novel possible glycobiomarker candidate by utilizing a glycoproteomics-based strategy. The serum level of WFA+-CSF1R in patients with hepatitis C virus (HCV)-infected liver disease was measured by an antibody-lectin sandwich ELISA. In a proof-of-concept experiment of the strategy preceding to future clinical studies, LC patients showed a high serum WFA+-CSF1R level in selected samples (P = 1.3 × 10–17). This result suggests WFA+-CSF1R is a possible biomarker candidate for evaluation of LC. Our results verified feasibility of this strategy for glycobiomarker development.
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ISSN:1535-3893
1535-3907
DOI:10.1021/pr400986t