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A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma.

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dc.contributor.author Gerdtsson, Anna S.
dc.contributor.author Malats i Riera, Núria
dc.contributor.author Säll, Anna
dc.contributor.author Real, Francisco X.
dc.contributor.author Porta Serra, Miquel
dc.contributor.author Skoog, Petter
dc.contributor.author Persson, Helena
dc.contributor.author Wingren, Christer
dc.contributor.author Borrebaeck, Carl A. K.
dc.date.accessioned 2016-02-03T12:45:12Z
dc.date.available 2016-02-03T12:45:12Z
dc.date.issued 2015
dc.identifier.citation Gerdtsson AS, Malats N, Säll A, Real FX, Porta M, Skoog P. et al. A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma. Int J Proteomics. 2015;2015:587250. DOI: 10.1155/2015/587250.
dc.identifier.issn 2090-2166
dc.identifier.uri http://hdl.handle.net/10230/25724
dc.description.abstract Background. Pancreatic ductal adenocarcinoma (PDAC) is an aggressive disease with rapid tumor progression and poor prognosis. This study was motivated by the lack of sensitive and specific PDAC biomarkers and aimed to identify a diagnostic, serum protein signature for PDAC. Methods. To mimic a real life test situation, a multicenter trial comprising a serum sample cohort, including 338 patients with either PDAC or other pancreatic diseases (OPD) and controls with nonpancreatic conditions (NPC), was analyzed on 293-plex recombinant antibody microarrays targeting immunoregulatory and cancer-associated antigens. Results. Serum samples collected from different hospitals were analyzed and showed that (i) sampling from five different hospitals could not be identified as a preanalytical variable and (ii) a multiplexed biomarker signature could be identified, utilizing up to 10 serum markers that could discriminate PDAC from controls, with sensitivities and specificities in the 91-100% range. The first protein profiles associated with the location of the primary tumor in the pancreas could also be identified. Conclusions. The results demonstrate that robust enough serum signatures could be identified in a multicenter trial, potentially contributing to the development of a multiplexed biomarker immunoassay for improved PDAC diagnosis.
dc.description.sponsorship This study was supported by VINNOVA and the SSF Strategic Center for Translational Cancer Research (CREATE Health); EU FP7 Grant Agreement 241481 (AFFINOMICS: Protein Binders for Characterization of Human Proteome Function: Generation, Validation, Application); Fondo de Investigaciones Sanitarias (FIS no. PI09-02102, no. PI12-00815, and no. PI13-00020) and Red Tematica de Investigación Cooperativa en Cancer (RTICC no. RD12/0036/0050), Instituto de Salud Carlos III (ISCIII), Spanish Ministry of Economy and Competitiveness; European Commission (EU-7FPHEALTH-259737 CANCERALIA) and European Cooperation in Science and Technology (COST Action no. BM1204: EU Pancreas).
dc.format.mimetype application/pdf
dc.language.iso eng
dc.publisher Hindawi Publishing Corporation
dc.relation.ispartof International Journal of Proteomics. 2015;2015:587250
dc.rights Copyright © 2015 Anna S. Gerdtsson et al. This is an open access article distributed under the http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly/ncited.
dc.rights.uri http://creativecommons.org/licenses/by/3.0/
dc.subject.other Pàncrees -- Càncer
dc.title A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma.
dc.type info:eu-repo/semantics/article
dc.identifier.doi http://dx.doi.org/10.1155/2015/587250
dc.relation.projectID info:eu-repo/grantAgreement/EC/FP7/241481
dc.relation.projectID info:eu-repo/granAgreement/EC/FP7/259737
dc.rights.accessRights info:eu-repo/semantics/openAccess
dc.type.version info:eu-repo/semantics/publishedVersion

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