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Using an Untargeted Metabolomics Approach to Identify Salivary Metabolites in Women with Breast Cancer
Metabolic alterations are a hallmark of the malignant transformation in cancer cells, which is characterized by multiple changes in metabolic pathways that are linked to macromolecule synthesis. This study aimed to explore whether salivary metabolites could help discriminate between breast cancer pa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763953/ https://www.ncbi.nlm.nih.gov/pubmed/33322065 http://dx.doi.org/10.3390/metabo10120506 |
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author | Xavier Assad, Daniele Acevedo, Ana Carolina Cançado Porto Mascarenhas, Elisa Costa Normando, Ana Gabriela Pichon, Valérie Chardin, Helene Neves Silva Guerra, Eliete Combes, Audrey |
author_facet | Xavier Assad, Daniele Acevedo, Ana Carolina Cançado Porto Mascarenhas, Elisa Costa Normando, Ana Gabriela Pichon, Valérie Chardin, Helene Neves Silva Guerra, Eliete Combes, Audrey |
author_sort | Xavier Assad, Daniele |
collection | PubMed |
description | Metabolic alterations are a hallmark of the malignant transformation in cancer cells, which is characterized by multiple changes in metabolic pathways that are linked to macromolecule synthesis. This study aimed to explore whether salivary metabolites could help discriminate between breast cancer patients and healthy controls. Saliva samples from 23 breast cancer patients and 35 healthy controls were subjected to untargeted metabolomics using liquid chromatography-quadrupole time-of-flight mass spectrometry and a bioinformatics tool (XCMS Online), which revealed 534 compounds, characterized by their retention time in reverse-phase liquid chromatography and by the m/z ratio detected, that were shared by the two groups. Using the METLIN database, 31 compounds that were upregulated in the breast cancer group (p < 0.05) were identified, including seven oligopeptides and six glycerophospholipids (PG14:2, PA32:1, PS28:0, PS40:6, PI31:1, and PI38:7). In addition, pre-treatment and post-treatment saliva samples were analyzed for 10 patients who experienced at least a partial response to their treatment. In these patients, three peptides and PG14:2 were upregulated before but not after treatment. The area under the curve, sensitivity, and specificity for PG14:2 was 0.7329, 65.22%, and 77.14%, respectively. These results provide new information regarding the salivary metabolite profiles of breast cancer patients, which may be useful biomarkers. |
format | Online Article Text |
id | pubmed-7763953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77639532020-12-27 Using an Untargeted Metabolomics Approach to Identify Salivary Metabolites in Women with Breast Cancer Xavier Assad, Daniele Acevedo, Ana Carolina Cançado Porto Mascarenhas, Elisa Costa Normando, Ana Gabriela Pichon, Valérie Chardin, Helene Neves Silva Guerra, Eliete Combes, Audrey Metabolites Article Metabolic alterations are a hallmark of the malignant transformation in cancer cells, which is characterized by multiple changes in metabolic pathways that are linked to macromolecule synthesis. This study aimed to explore whether salivary metabolites could help discriminate between breast cancer patients and healthy controls. Saliva samples from 23 breast cancer patients and 35 healthy controls were subjected to untargeted metabolomics using liquid chromatography-quadrupole time-of-flight mass spectrometry and a bioinformatics tool (XCMS Online), which revealed 534 compounds, characterized by their retention time in reverse-phase liquid chromatography and by the m/z ratio detected, that were shared by the two groups. Using the METLIN database, 31 compounds that were upregulated in the breast cancer group (p < 0.05) were identified, including seven oligopeptides and six glycerophospholipids (PG14:2, PA32:1, PS28:0, PS40:6, PI31:1, and PI38:7). In addition, pre-treatment and post-treatment saliva samples were analyzed for 10 patients who experienced at least a partial response to their treatment. In these patients, three peptides and PG14:2 were upregulated before but not after treatment. The area under the curve, sensitivity, and specificity for PG14:2 was 0.7329, 65.22%, and 77.14%, respectively. These results provide new information regarding the salivary metabolite profiles of breast cancer patients, which may be useful biomarkers. MDPI 2020-12-10 /pmc/articles/PMC7763953/ /pubmed/33322065 http://dx.doi.org/10.3390/metabo10120506 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Xavier Assad, Daniele Acevedo, Ana Carolina Cançado Porto Mascarenhas, Elisa Costa Normando, Ana Gabriela Pichon, Valérie Chardin, Helene Neves Silva Guerra, Eliete Combes, Audrey Using an Untargeted Metabolomics Approach to Identify Salivary Metabolites in Women with Breast Cancer |
title | Using an Untargeted Metabolomics Approach to Identify Salivary Metabolites in Women with Breast Cancer |
title_full | Using an Untargeted Metabolomics Approach to Identify Salivary Metabolites in Women with Breast Cancer |
title_fullStr | Using an Untargeted Metabolomics Approach to Identify Salivary Metabolites in Women with Breast Cancer |
title_full_unstemmed | Using an Untargeted Metabolomics Approach to Identify Salivary Metabolites in Women with Breast Cancer |
title_short | Using an Untargeted Metabolomics Approach to Identify Salivary Metabolites in Women with Breast Cancer |
title_sort | using an untargeted metabolomics approach to identify salivary metabolites in women with breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763953/ https://www.ncbi.nlm.nih.gov/pubmed/33322065 http://dx.doi.org/10.3390/metabo10120506 |
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