Journal of Proteome Research · 2006 · 222 citations · 17 references
Life SciencesBiochemistryOncologyGlycobiologyMolecular OncologyProteomicsCancer GlycobiologyGlycan AnalysisGlycoproteomicsHepatocellular CarcinomaLiver CancerProtein GlycosylationAberrant Glycosylation In CancerFucosylation In CancerGlycoproteomic BiomarkersHepatocellular Carcinoma PathogenesisN-glycan Core FucosylationPrimary Liver CancerProtein Glycosylation In OncogenesisTumor-associated Glycoproteins
Changes in N-linked glycosylation are known to occur during the development of cancer. For example, increased branching of oligosaccharides has been associated with metastasis and has been correlated to tumor progression in human cancers of the breast, colon and melanomas. Increases in core fucosylation have also been associated with the development of hepatocellular carcinoma (HCC). Chronic infection with the hepatitis B virus is associated with more than 55% of all cases of hepatocellular carcinoma. We show here that increased levels of core fucosylation can be observed via glycan analysis of total serum and are associated with the development of HCC. In a blinded study, the serum glycoproteins derived from people diagnosed with HBV induced liver cancer were found to possess a dramatically higher level of fucosylation. This change occurs on both immunoglobulin molecules and on other serum glycoproteins. Targeted glycoproteomic analysis was used to identify those glycoproteins that are hyperfucosylated in cancer. In total, 19 proteins were found to be hyperfucosylated in cancer. The potential of these proteins as biomarkers of cancer is discussed.
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Timothy M. Block, Mary Ann Comunale, Melissa Lowman et al. · Proceedings of the National Academy of Sciences · 2005 · 370 citations · Full text