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Detection of candidate biomarkers of prostate cancer progression in serum: a depletion-free 3D LC/MS quantitative proteomics pilot study
BACKGROUND: Prostate cancer (PCa) is the most common male cancer in the United Kingdom and we aimed to identify clinically relevant biomarkers corresponding to stage progression of the disease. METHODS: We used enhanced proteomic profiling of PCa progression using iTRAQ 3D LC mass spectrometry on hi...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117786/ https://www.ncbi.nlm.nih.gov/pubmed/27685442 http://dx.doi.org/10.1038/bjc.2016.291 |
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author | Larkin, S E T Johnston, H E Jackson, T R Jamieson, D G Roumeliotis, T I Mockridge, C I Michael, A Manousopoulou, A Papachristou, E K Brown, M D Clarke, N W Pandha, H Aukim-Hastie, C L Cragg, M S Garbis, S D Townsend, P A |
author_facet | Larkin, S E T Johnston, H E Jackson, T R Jamieson, D G Roumeliotis, T I Mockridge, C I Michael, A Manousopoulou, A Papachristou, E K Brown, M D Clarke, N W Pandha, H Aukim-Hastie, C L Cragg, M S Garbis, S D Townsend, P A |
author_sort | Larkin, S E T |
collection | PubMed |
description | BACKGROUND: Prostate cancer (PCa) is the most common male cancer in the United Kingdom and we aimed to identify clinically relevant biomarkers corresponding to stage progression of the disease. METHODS: We used enhanced proteomic profiling of PCa progression using iTRAQ 3D LC mass spectrometry on high-quality serum samples to identify biomarkers of PCa. RESULTS: We identified >1000 proteins. Following specific inclusion/exclusion criteria we targeted seven proteins of which two were validated by ELISA and six potentially interacted forming an ‘interactome' with only a single protein linking each marker. This network also includes accepted cancer markers, such as TNF, STAT3, NF-κB and IL6. CONCLUSIONS: Our linked and interrelated biomarker network highlights the potential utility of six of our seven markers as a panel for diagnosing PCa and, critically, in determining the stage of the disease. Our validation analysis of the MS-identified proteins found that SAA alongside KLK3 may improve categorisation of PCa than by KLK3 alone, and that TSR1, although not significant in this model, might also be a clinically relevant biomarker. |
format | Online Article Text |
id | pubmed-5117786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51177862016-12-16 Detection of candidate biomarkers of prostate cancer progression in serum: a depletion-free 3D LC/MS quantitative proteomics pilot study Larkin, S E T Johnston, H E Jackson, T R Jamieson, D G Roumeliotis, T I Mockridge, C I Michael, A Manousopoulou, A Papachristou, E K Brown, M D Clarke, N W Pandha, H Aukim-Hastie, C L Cragg, M S Garbis, S D Townsend, P A Br J Cancer Molecular Diagnostics BACKGROUND: Prostate cancer (PCa) is the most common male cancer in the United Kingdom and we aimed to identify clinically relevant biomarkers corresponding to stage progression of the disease. METHODS: We used enhanced proteomic profiling of PCa progression using iTRAQ 3D LC mass spectrometry on high-quality serum samples to identify biomarkers of PCa. RESULTS: We identified >1000 proteins. Following specific inclusion/exclusion criteria we targeted seven proteins of which two were validated by ELISA and six potentially interacted forming an ‘interactome' with only a single protein linking each marker. This network also includes accepted cancer markers, such as TNF, STAT3, NF-κB and IL6. CONCLUSIONS: Our linked and interrelated biomarker network highlights the potential utility of six of our seven markers as a panel for diagnosing PCa and, critically, in determining the stage of the disease. Our validation analysis of the MS-identified proteins found that SAA alongside KLK3 may improve categorisation of PCa than by KLK3 alone, and that TSR1, although not significant in this model, might also be a clinically relevant biomarker. Nature Publishing Group 2016-10-25 2016-09-29 /pmc/articles/PMC5117786/ /pubmed/27685442 http://dx.doi.org/10.1038/bjc.2016.291 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Molecular Diagnostics Larkin, S E T Johnston, H E Jackson, T R Jamieson, D G Roumeliotis, T I Mockridge, C I Michael, A Manousopoulou, A Papachristou, E K Brown, M D Clarke, N W Pandha, H Aukim-Hastie, C L Cragg, M S Garbis, S D Townsend, P A Detection of candidate biomarkers of prostate cancer progression in serum: a depletion-free 3D LC/MS quantitative proteomics pilot study |
title | Detection of candidate biomarkers of prostate cancer progression in serum: a depletion-free 3D LC/MS quantitative proteomics pilot study |
title_full | Detection of candidate biomarkers of prostate cancer progression in serum: a depletion-free 3D LC/MS quantitative proteomics pilot study |
title_fullStr | Detection of candidate biomarkers of prostate cancer progression in serum: a depletion-free 3D LC/MS quantitative proteomics pilot study |
title_full_unstemmed | Detection of candidate biomarkers of prostate cancer progression in serum: a depletion-free 3D LC/MS quantitative proteomics pilot study |
title_short | Detection of candidate biomarkers of prostate cancer progression in serum: a depletion-free 3D LC/MS quantitative proteomics pilot study |
title_sort | detection of candidate biomarkers of prostate cancer progression in serum: a depletion-free 3d lc/ms quantitative proteomics pilot study |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117786/ https://www.ncbi.nlm.nih.gov/pubmed/27685442 http://dx.doi.org/10.1038/bjc.2016.291 |
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