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Patients with early-stage oropharyngeal cancer can be identified with label-free serum proteomics
BACKGROUND: The increasing incidence of oropharyngeal squamous cell carcinoma (OPSCC) is mainly related to human papillomavirus (HPV) infection. As OPSCCs are often diagnosed at an advanced stage, mortality and morbidity remain high. There are no diagnostic biomarkers for early detection of OPSCC. M...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048110/ https://www.ncbi.nlm.nih.gov/pubmed/29961760 http://dx.doi.org/10.1038/s41416-018-0162-2 |
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author | Tuhkuri, Anna Saraswat, Mayank Mäkitie, Antti Mattila, Petri Silén, Robert Dickinson, Amy Carpén, Timo Tohmola, Tiialotta Joenväärä, Sakari Renkonen, Suvi |
author_facet | Tuhkuri, Anna Saraswat, Mayank Mäkitie, Antti Mattila, Petri Silén, Robert Dickinson, Amy Carpén, Timo Tohmola, Tiialotta Joenväärä, Sakari Renkonen, Suvi |
author_sort | Tuhkuri, Anna |
collection | PubMed |
description | BACKGROUND: The increasing incidence of oropharyngeal squamous cell carcinoma (OPSCC) is mainly related to human papillomavirus (HPV) infection. As OPSCCs are often diagnosed at an advanced stage, mortality and morbidity remain high. There are no diagnostic biomarkers for early detection of OPSCC. METHODS: Serum from 25 patients with stage I–II OPSCC, and 12 healthy controls, was studied with quantitative label-free proteomics using ultra-definition MS(E). Statistical analyses were performed to identify the proteins most reliably distinguishing early-stage OPSCCs from controls. P16 was used as a surrogate marker for HPV. P16-positive and P16-negative tumours were analysed separately. RESULTS: With two or more unique proteins per identification, 176 proteins were quantified. A clear separation between patients with early-stage tumours and controls was seen in principal component analysis. Latent structures discriminant analysis identified 96 proteins, most reliably differentiating OPSCC patients from controls, with 13 upregulated and 83 downregulated proteins in study cases. The set of proteins was studied further with network, pathway and protein–protein interaction analyses, and found to participate in lipid metabolism, for example. CONCLUSIONS: We found a set of serum proteins distinguishing early-stage OPSCC from healthy individuals, and suggest a protein set for further evaluation as a diagnostic biomarker panel for OPSCC. |
format | Online Article Text |
id | pubmed-6048110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60481102019-07-17 Patients with early-stage oropharyngeal cancer can be identified with label-free serum proteomics Tuhkuri, Anna Saraswat, Mayank Mäkitie, Antti Mattila, Petri Silén, Robert Dickinson, Amy Carpén, Timo Tohmola, Tiialotta Joenväärä, Sakari Renkonen, Suvi Br J Cancer Article BACKGROUND: The increasing incidence of oropharyngeal squamous cell carcinoma (OPSCC) is mainly related to human papillomavirus (HPV) infection. As OPSCCs are often diagnosed at an advanced stage, mortality and morbidity remain high. There are no diagnostic biomarkers for early detection of OPSCC. METHODS: Serum from 25 patients with stage I–II OPSCC, and 12 healthy controls, was studied with quantitative label-free proteomics using ultra-definition MS(E). Statistical analyses were performed to identify the proteins most reliably distinguishing early-stage OPSCCs from controls. P16 was used as a surrogate marker for HPV. P16-positive and P16-negative tumours were analysed separately. RESULTS: With two or more unique proteins per identification, 176 proteins were quantified. A clear separation between patients with early-stage tumours and controls was seen in principal component analysis. Latent structures discriminant analysis identified 96 proteins, most reliably differentiating OPSCC patients from controls, with 13 upregulated and 83 downregulated proteins in study cases. The set of proteins was studied further with network, pathway and protein–protein interaction analyses, and found to participate in lipid metabolism, for example. CONCLUSIONS: We found a set of serum proteins distinguishing early-stage OPSCC from healthy individuals, and suggest a protein set for further evaluation as a diagnostic biomarker panel for OPSCC. Nature Publishing Group UK 2018-07-02 2018-07-17 /pmc/articles/PMC6048110/ /pubmed/29961760 http://dx.doi.org/10.1038/s41416-018-0162-2 Text en © Cancer Research UK 2018 https://creativecommons.org/licenses/by/4.0/This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0). |
spellingShingle | Article Tuhkuri, Anna Saraswat, Mayank Mäkitie, Antti Mattila, Petri Silén, Robert Dickinson, Amy Carpén, Timo Tohmola, Tiialotta Joenväärä, Sakari Renkonen, Suvi Patients with early-stage oropharyngeal cancer can be identified with label-free serum proteomics |
title | Patients with early-stage oropharyngeal cancer can be identified with label-free serum proteomics |
title_full | Patients with early-stage oropharyngeal cancer can be identified with label-free serum proteomics |
title_fullStr | Patients with early-stage oropharyngeal cancer can be identified with label-free serum proteomics |
title_full_unstemmed | Patients with early-stage oropharyngeal cancer can be identified with label-free serum proteomics |
title_short | Patients with early-stage oropharyngeal cancer can be identified with label-free serum proteomics |
title_sort | patients with early-stage oropharyngeal cancer can be identified with label-free serum proteomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048110/ https://www.ncbi.nlm.nih.gov/pubmed/29961760 http://dx.doi.org/10.1038/s41416-018-0162-2 |
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