| Literature DB >> 29847809 |
Tatjana Sajic1, Yansheng Liu2, Eirini Arvaniti3, Silvia Surinova4, Evan G Williams5, Ralph Schiess6, Ruth Hüttenhain7, Atul Sethi8, Sheng Pan9, Teresa A Brentnall10, Ru Chen10, Peter Blattmann5, Betty Friedrich3, Emma Niméus11, Susanne Malander12, Aurelius Omlin13, Silke Gillessen13, Manfred Claassen5, Ruedi Aebersold14.
Abstract
Cancer is mostly incurable when diagnosed at a metastatic stage, making its early detection via blood proteins of immense clinical interest. Proteomic changes in tumor tissue may lead to changes detectable in the protein composition of circulating blood plasma. Using a proteomic workflow combining N-glycosite enrichment and SWATH mass spectrometry, we generate a data resource of 284 blood samples derived from patients with different types of localized-stage carcinomas and from matched controls. We observe whether the changes in the patient's plasma are specific to a particular carcinoma or represent a generic signature of proteins modified uniformly in a common, systemic response to many cancers. A quantitative comparison of the resulting N-glycosite profiles discovers that proteins related to blood platelets are common to several cancers (e.g., THBS1), whereas others are highly cancer-type specific. Available proteomics data, including a SWATH library to study N-glycoproteins, will facilitate follow-up biomarker research into early cancer detection.Entities:
Keywords: SWATH-mass spectrometry; blood; carcinoma; glycoproteins; human clinical study; localized cancer; secreted
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Year: 2018 PMID: 29847809 DOI: 10.1016/j.celrep.2018.04.114
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423