Seromic profiling of colorectal cancer patients with novel glycopeptide microarray

Johannes Wirenfeldt Vad Pedersen, Ola Blixt, Eric Paul Bennett, Mads Peter Agervig Tarp, Imran Parvez Dar, Ulla Mandel, Steen Seier Poulsen, Anders E Pedersen, Susanne Rasmussen, Per Jess, Henrik Clausen, Hans H. Wandall

122 Citationer (Scopus)


Cancer-associated autoantibodies hold promise as sensitive biomarkers for early detection of cancer. Aberrant post-translational variants of proteins are likely to induce autoantibodies, and changes in O-linked glycosylation represent one of the most important cancer-associated post-translational modifications (PTMs). Short aberrant O-glycans on proteins may introduce novel glycopeptide epitopes that can elicit autoantibodies because of lack of tolerance. Technical barriers, however, have hampered detection of such glycopeptide-specific autoantibodies. Here, we have constructed an expanded glycopeptide array displaying a comprehensive library of glycopeptides and glycoproteins derived from a panel of human mucins (MUC1, MUC2, MUC4, MUC5AC, MUC6 and MUC7) known to have altered glycosylation and expression in cancer. Seromic profiling of patients with colorectal cancer identified cancer-associated autoantibodies to a set of aberrant glycopeptides derived from MUC1 and MUC4. The cumulative sensitivity of the array analysis was 79% with a specificity of 92%. The most prevalent of the identified autoantibody targets were validated as authentic cancer immunogens by showing expression of the epitopes in cancer using novel monoclonal antibodies. Our study provides evidence for the value of glycopeptides and other PTM-peptide arrays in diagnostic measures.
TidsskriftInternational Journal of Cancer
Udgave nummer8
Sider (fra-til)1860-71
Antal sider12
StatusUdgivet - 15 apr. 2011


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