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Serum apolipoprotein C-II is prognostic for survival after pancreatic resection for adenocarcinoma

BACKGROUND: Pancreaticoduodenectomy remains a major undertaking. A preoperative blood test, which could confidently predict the benefits of surgery would improve the selection of pancreatic cancer patients for surgery. This study aimed to identify protein biomarkers prognostic for long-term survival...

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Autores principales: Xue, A, Chang, J W, Chung, L, Samra, J, Hugh, T, Gill, A, Butturini, G, Baxter, R C, Smith, R C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504954/
https://www.ncbi.nlm.nih.gov/pubmed/23169340
http://dx.doi.org/10.1038/bjc.2012.458
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author Xue, A
Chang, J W
Chung, L
Samra, J
Hugh, T
Gill, A
Butturini, G
Baxter, R C
Smith, R C
author_facet Xue, A
Chang, J W
Chung, L
Samra, J
Hugh, T
Gill, A
Butturini, G
Baxter, R C
Smith, R C
author_sort Xue, A
collection PubMed
description BACKGROUND: Pancreaticoduodenectomy remains a major undertaking. A preoperative blood test, which could confidently predict the benefits of surgery would improve the selection of pancreatic cancer patients for surgery. This study aimed to identify protein biomarkers prognostic for long-term survival and to validate them with clinico-pathological information. METHODS: Serum from 40 preoperative patients was used to train for predictive biomarkers using surface-enhanced laser desorption/ionisation time-of-flight mass spectrometry (SELDI), and the results were verified on 21 independent samples. Two predictive proteins were identified by tryptic peptide mass fingerprinting and sequencing, and validated on serum from another 57 patients by enzyme-linked immunosorbent assay (ELISA). The influence of these proteins on growth and invasion of two cancer cell lines was tested in-vitro. RESULTS: The SELDI panel of m/z 3700, 8222 and 11 522 peaks predicted <12 months’ survival (ROC AUC: 0.79, 0.64–0.90; P<0.039). When CA19-9 was added, the ROC AUC increased to 0.95 (0.84–0.99; P<0.0001). The six subjects in the verification group who died within 12 months were correctly classified. The m/z 8222 and 11 522 proteins were identified as Serum ApoC-II and SAA-1, respectively. In the validation samples, ELISA results confirmed that ApoC-II was predictive of survival (Kaplan–Meier P<0.009), but not SAA-I. ApoC-II, CA19-9 and major-vessel involvement independently predicted survival. ApoC-II and SAA-1 increased cell growth and invasion of both cancer cell lines. CONCLUSION: Serum ApoC-II, CA19-9 and major-vessel invasion independently predict survival and improves selection of patients for pancreaticoduodenectomy.
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spelling pubmed-35049542013-11-20 Serum apolipoprotein C-II is prognostic for survival after pancreatic resection for adenocarcinoma Xue, A Chang, J W Chung, L Samra, J Hugh, T Gill, A Butturini, G Baxter, R C Smith, R C Br J Cancer Molecular Diagnostics BACKGROUND: Pancreaticoduodenectomy remains a major undertaking. A preoperative blood test, which could confidently predict the benefits of surgery would improve the selection of pancreatic cancer patients for surgery. This study aimed to identify protein biomarkers prognostic for long-term survival and to validate them with clinico-pathological information. METHODS: Serum from 40 preoperative patients was used to train for predictive biomarkers using surface-enhanced laser desorption/ionisation time-of-flight mass spectrometry (SELDI), and the results were verified on 21 independent samples. Two predictive proteins were identified by tryptic peptide mass fingerprinting and sequencing, and validated on serum from another 57 patients by enzyme-linked immunosorbent assay (ELISA). The influence of these proteins on growth and invasion of two cancer cell lines was tested in-vitro. RESULTS: The SELDI panel of m/z 3700, 8222 and 11 522 peaks predicted <12 months’ survival (ROC AUC: 0.79, 0.64–0.90; P<0.039). When CA19-9 was added, the ROC AUC increased to 0.95 (0.84–0.99; P<0.0001). The six subjects in the verification group who died within 12 months were correctly classified. The m/z 8222 and 11 522 proteins were identified as Serum ApoC-II and SAA-1, respectively. In the validation samples, ELISA results confirmed that ApoC-II was predictive of survival (Kaplan–Meier P<0.009), but not SAA-I. ApoC-II, CA19-9 and major-vessel involvement independently predicted survival. ApoC-II and SAA-1 increased cell growth and invasion of both cancer cell lines. CONCLUSION: Serum ApoC-II, CA19-9 and major-vessel invasion independently predict survival and improves selection of patients for pancreaticoduodenectomy. Nature Publishing Group 2012-11-20 2012-11-20 /pmc/articles/PMC3504954/ /pubmed/23169340 http://dx.doi.org/10.1038/bjc.2012.458 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by-nc-sa/3.0/From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Molecular Diagnostics
Xue, A
Chang, J W
Chung, L
Samra, J
Hugh, T
Gill, A
Butturini, G
Baxter, R C
Smith, R C
Serum apolipoprotein C-II is prognostic for survival after pancreatic resection for adenocarcinoma
title Serum apolipoprotein C-II is prognostic for survival after pancreatic resection for adenocarcinoma
title_full Serum apolipoprotein C-II is prognostic for survival after pancreatic resection for adenocarcinoma
title_fullStr Serum apolipoprotein C-II is prognostic for survival after pancreatic resection for adenocarcinoma
title_full_unstemmed Serum apolipoprotein C-II is prognostic for survival after pancreatic resection for adenocarcinoma
title_short Serum apolipoprotein C-II is prognostic for survival after pancreatic resection for adenocarcinoma
title_sort serum apolipoprotein c-ii is prognostic for survival after pancreatic resection for adenocarcinoma
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504954/
https://www.ncbi.nlm.nih.gov/pubmed/23169340
http://dx.doi.org/10.1038/bjc.2012.458
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