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Plasma metabolomics of oral squamous cell carcinomas based on NMR and MS approaches provides biomarker identification and survival prediction

Metabolomics has proven to be an important omics approach to understand the molecular pathways underlying the tumour phenotype and to identify new clinically useful markers. The literature on cancer has illustrated the potential of this approach as a diagnostic and prognostic tool. The present study...

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Autores principales: Polachini, Giovana Mussi, de Castro, Tialfi Bergamin, Smarra, Luis Fabiano Soares, Henrique, Tiago, de Paula, Carlos Henrique Diniz, Severino, Patricia, López, Rossana Veronica Mendoza, Carvalho, André Lopes, de Mattos Zeri, Ana Carolina, Silva, Ismael Dale Cotrim Guerreiro, Tajara, Eloiza H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220089/
https://www.ncbi.nlm.nih.gov/pubmed/37237049
http://dx.doi.org/10.1038/s41598-023-34808-2
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author Polachini, Giovana Mussi
de Castro, Tialfi Bergamin
Smarra, Luis Fabiano Soares
Henrique, Tiago
de Paula, Carlos Henrique Diniz
Severino, Patricia
López, Rossana Veronica Mendoza
Carvalho, André Lopes
de Mattos Zeri, Ana Carolina
Silva, Ismael Dale Cotrim Guerreiro
Tajara, Eloiza H.
author_facet Polachini, Giovana Mussi
de Castro, Tialfi Bergamin
Smarra, Luis Fabiano Soares
Henrique, Tiago
de Paula, Carlos Henrique Diniz
Severino, Patricia
López, Rossana Veronica Mendoza
Carvalho, André Lopes
de Mattos Zeri, Ana Carolina
Silva, Ismael Dale Cotrim Guerreiro
Tajara, Eloiza H.
author_sort Polachini, Giovana Mussi
collection PubMed
description Metabolomics has proven to be an important omics approach to understand the molecular pathways underlying the tumour phenotype and to identify new clinically useful markers. The literature on cancer has illustrated the potential of this approach as a diagnostic and prognostic tool. The present study aimed to analyse the plasma metabolic profile of patients with oral squamous cell carcinoma (OSCC) and controls and to compare patients with metastatic and primary tumours at different stages and subsites using nuclear magnetic resonance and mass spectrometry. To our knowledge, this is the only report that compared patients at different stages and subsites and replicates collected in diverse institutions at different times using these methodologies. Our results showed a plasma metabolic OSCC profile suggestive of abnormal ketogenesis, lipogenesis and energy metabolism, which is already present in early phases but is more evident in advanced stages of the disease. Reduced levels of several metabolites were also associated with an unfavorable prognosis. The observed metabolomic alterations may contribute to inflammation, immune response inhibition and tumour growth, and may be explained by four nonexclusive views—differential synthesis, uptake, release, and degradation of metabolites. The interpretation that assimilates these views is the cross talk between neoplastic and normal cells in the tumour microenvironment or in more distant anatomical sites, connected by biofluids, signalling molecules and vesicles. Additional population samples to evaluate the details of these molecular processes may lead to the discovery of new biomarkers and novel strategies for OSCC prevention and treatment.
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spelling pubmed-102200892023-05-28 Plasma metabolomics of oral squamous cell carcinomas based on NMR and MS approaches provides biomarker identification and survival prediction Polachini, Giovana Mussi de Castro, Tialfi Bergamin Smarra, Luis Fabiano Soares Henrique, Tiago de Paula, Carlos Henrique Diniz Severino, Patricia López, Rossana Veronica Mendoza Carvalho, André Lopes de Mattos Zeri, Ana Carolina Silva, Ismael Dale Cotrim Guerreiro Tajara, Eloiza H. Sci Rep Article Metabolomics has proven to be an important omics approach to understand the molecular pathways underlying the tumour phenotype and to identify new clinically useful markers. The literature on cancer has illustrated the potential of this approach as a diagnostic and prognostic tool. The present study aimed to analyse the plasma metabolic profile of patients with oral squamous cell carcinoma (OSCC) and controls and to compare patients with metastatic and primary tumours at different stages and subsites using nuclear magnetic resonance and mass spectrometry. To our knowledge, this is the only report that compared patients at different stages and subsites and replicates collected in diverse institutions at different times using these methodologies. Our results showed a plasma metabolic OSCC profile suggestive of abnormal ketogenesis, lipogenesis and energy metabolism, which is already present in early phases but is more evident in advanced stages of the disease. Reduced levels of several metabolites were also associated with an unfavorable prognosis. The observed metabolomic alterations may contribute to inflammation, immune response inhibition and tumour growth, and may be explained by four nonexclusive views—differential synthesis, uptake, release, and degradation of metabolites. The interpretation that assimilates these views is the cross talk between neoplastic and normal cells in the tumour microenvironment or in more distant anatomical sites, connected by biofluids, signalling molecules and vesicles. Additional population samples to evaluate the details of these molecular processes may lead to the discovery of new biomarkers and novel strategies for OSCC prevention and treatment. Nature Publishing Group UK 2023-05-26 /pmc/articles/PMC10220089/ /pubmed/37237049 http://dx.doi.org/10.1038/s41598-023-34808-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Polachini, Giovana Mussi
de Castro, Tialfi Bergamin
Smarra, Luis Fabiano Soares
Henrique, Tiago
de Paula, Carlos Henrique Diniz
Severino, Patricia
López, Rossana Veronica Mendoza
Carvalho, André Lopes
de Mattos Zeri, Ana Carolina
Silva, Ismael Dale Cotrim Guerreiro
Tajara, Eloiza H.
Plasma metabolomics of oral squamous cell carcinomas based on NMR and MS approaches provides biomarker identification and survival prediction
title Plasma metabolomics of oral squamous cell carcinomas based on NMR and MS approaches provides biomarker identification and survival prediction
title_full Plasma metabolomics of oral squamous cell carcinomas based on NMR and MS approaches provides biomarker identification and survival prediction
title_fullStr Plasma metabolomics of oral squamous cell carcinomas based on NMR and MS approaches provides biomarker identification and survival prediction
title_full_unstemmed Plasma metabolomics of oral squamous cell carcinomas based on NMR and MS approaches provides biomarker identification and survival prediction
title_short Plasma metabolomics of oral squamous cell carcinomas based on NMR and MS approaches provides biomarker identification and survival prediction
title_sort plasma metabolomics of oral squamous cell carcinomas based on nmr and ms approaches provides biomarker identification and survival prediction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220089/
https://www.ncbi.nlm.nih.gov/pubmed/37237049
http://dx.doi.org/10.1038/s41598-023-34808-2
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