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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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.
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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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