作者: David S. Williams , Matthew J. Bird , Robert N. Jorissen , Yen Lin Yu , Franscesa Walker
DOI: 10.1371/JOURNAL.PONE.0016012
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摘要: Background Frameshift mutations in microsatellite instability high (MSI-High) colorectal cancers are a potential source of targetable neo-antigens. Many nonsense transcripts subject to rapid degradation due nonsense-mediated decay (NMD), but with cMS the last exon or near exon-exon junction have intrinsic resistance (NMD). NMD-resistant therefore likely expressed mutant proteins MSI-High tumours.