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Identification of potential serum peptide biomarkers of biliary tract cancer using MALDI MS profiling
BACKGROUND: The aim of this discovery study was the identification of peptide serum biomarkers for detecting biliary tract cancer (BTC) using samples from healthy volunteers and benign cases of biliary disease as control groups. This work was based on the hypothesis that cancer-specific exopeptidase...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923428/ https://www.ncbi.nlm.nih.gov/pubmed/24495412 http://dx.doi.org/10.1186/1472-6890-14-7 |
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author | Sandanayake, Neomal S Camuzeaux, Stephane Sinclair, John Blyuss, Oleg Andreola, Fausto Chapman, Michael H Webster, George J Smith, Ross C Timms, John F Pereira, Stephen P |
author_facet | Sandanayake, Neomal S Camuzeaux, Stephane Sinclair, John Blyuss, Oleg Andreola, Fausto Chapman, Michael H Webster, George J Smith, Ross C Timms, John F Pereira, Stephen P |
author_sort | Sandanayake, Neomal S |
collection | PubMed |
description | BACKGROUND: The aim of this discovery study was the identification of peptide serum biomarkers for detecting biliary tract cancer (BTC) using samples from healthy volunteers and benign cases of biliary disease as control groups. This work was based on the hypothesis that cancer-specific exopeptidases exist and that their activities in serum can generate cancer-predictive peptide fragments from circulating proteins during coagulation. METHODS: This case control study used a semi-automated platform incorporating polypeptide extraction linked to matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF MS) to profile 92 patient serum samples. Predictive models were generated to test a validation serum set from BTC cases and healthy volunteers. RESULTS: Several peptide peaks were found that could significantly differentiate BTC patients from healthy controls and benign biliary disease. A predictive model resulted in a sensitivity of 100% and a specificity of 93.8% in detecting BTC in the validation set, whilst another model gave a sensitivity of 79.5% and a specificity of 83.9% in discriminating BTC from benign biliary disease samples in the training set. Discriminatory peaks were identified by tandem MS as fragments of abundant clotting proteins. CONCLUSIONS: Serum MALDI MS peptide signatures can accurately discriminate patients with BTC from healthy volunteers. |
format | Online Article Text |
id | pubmed-3923428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39234282014-02-14 Identification of potential serum peptide biomarkers of biliary tract cancer using MALDI MS profiling Sandanayake, Neomal S Camuzeaux, Stephane Sinclair, John Blyuss, Oleg Andreola, Fausto Chapman, Michael H Webster, George J Smith, Ross C Timms, John F Pereira, Stephen P BMC Clin Pathol Research Article BACKGROUND: The aim of this discovery study was the identification of peptide serum biomarkers for detecting biliary tract cancer (BTC) using samples from healthy volunteers and benign cases of biliary disease as control groups. This work was based on the hypothesis that cancer-specific exopeptidases exist and that their activities in serum can generate cancer-predictive peptide fragments from circulating proteins during coagulation. METHODS: This case control study used a semi-automated platform incorporating polypeptide extraction linked to matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF MS) to profile 92 patient serum samples. Predictive models were generated to test a validation serum set from BTC cases and healthy volunteers. RESULTS: Several peptide peaks were found that could significantly differentiate BTC patients from healthy controls and benign biliary disease. A predictive model resulted in a sensitivity of 100% and a specificity of 93.8% in detecting BTC in the validation set, whilst another model gave a sensitivity of 79.5% and a specificity of 83.9% in discriminating BTC from benign biliary disease samples in the training set. Discriminatory peaks were identified by tandem MS as fragments of abundant clotting proteins. CONCLUSIONS: Serum MALDI MS peptide signatures can accurately discriminate patients with BTC from healthy volunteers. BioMed Central 2014-02-04 /pmc/articles/PMC3923428/ /pubmed/24495412 http://dx.doi.org/10.1186/1472-6890-14-7 Text en Copyright © 2014 Sandanayake et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sandanayake, Neomal S Camuzeaux, Stephane Sinclair, John Blyuss, Oleg Andreola, Fausto Chapman, Michael H Webster, George J Smith, Ross C Timms, John F Pereira, Stephen P Identification of potential serum peptide biomarkers of biliary tract cancer using MALDI MS profiling |
title | Identification of potential serum peptide biomarkers of biliary tract cancer using MALDI MS profiling |
title_full | Identification of potential serum peptide biomarkers of biliary tract cancer using MALDI MS profiling |
title_fullStr | Identification of potential serum peptide biomarkers of biliary tract cancer using MALDI MS profiling |
title_full_unstemmed | Identification of potential serum peptide biomarkers of biliary tract cancer using MALDI MS profiling |
title_short | Identification of potential serum peptide biomarkers of biliary tract cancer using MALDI MS profiling |
title_sort | identification of potential serum peptide biomarkers of biliary tract cancer using maldi ms profiling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923428/ https://www.ncbi.nlm.nih.gov/pubmed/24495412 http://dx.doi.org/10.1186/1472-6890-14-7 |
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