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

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...

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Autores principales: Gerdtsson, Anna S., Malats, Núria, Säll, Anna, Real, Francisco X., Porta, Miquel, Skoog, Petter, Persson, Helena, Wingren, Christer, Borrebaeck, Carl A. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637476/
https://www.ncbi.nlm.nih.gov/pubmed/26587286
http://dx.doi.org/10.1155/2015/587250
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author Gerdtsson, Anna S.
Malats, Núria
Säll, Anna
Real, Francisco X.
Porta, Miquel
Skoog, Petter
Persson, Helena
Wingren, Christer
Borrebaeck, Carl A. K.
author_facet Gerdtsson, Anna S.
Malats, Núria
Säll, Anna
Real, Francisco X.
Porta, Miquel
Skoog, Petter
Persson, Helena
Wingren, Christer
Borrebaeck, Carl A. K.
author_sort Gerdtsson, Anna S.
collection PubMed
description 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.
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spelling pubmed-46374762015-11-19 A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma Gerdtsson, Anna S. Malats, Núria Säll, Anna Real, Francisco X. Porta, Miquel Skoog, Petter Persson, Helena Wingren, Christer Borrebaeck, Carl A. K. Int J Proteomics Research Article 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. Hindawi Publishing Corporation 2015 2015-10-26 /pmc/articles/PMC4637476/ /pubmed/26587286 http://dx.doi.org/10.1155/2015/587250 Text en Copyright © 2015 Anna S. Gerdtsson et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gerdtsson, Anna S.
Malats, Núria
Säll, Anna
Real, Francisco X.
Porta, Miquel
Skoog, Petter
Persson, Helena
Wingren, Christer
Borrebaeck, Carl A. K.
A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma
title A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma
title_full A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma
title_fullStr A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma
title_full_unstemmed A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma
title_short A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma
title_sort multicenter trial defining a serum protein signature associated with pancreatic ductal adenocarcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637476/
https://www.ncbi.nlm.nih.gov/pubmed/26587286
http://dx.doi.org/10.1155/2015/587250
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