Cargando…

Expression of Glycolysis-Related Proteins in Cancer of Unknown Primary Origin

INTRODUCTION: Cancer of unknown primary origin (CUP) is defined as metastatic cancer without identification of the primary site. Considering that only 15–20% of patients with CUP show a favorable outcome, identifying biomarkers may help improve the clinical management of patients who do not respond...

Descripción completa

Detalles Bibliográficos
Autores principales: Bonatelli, Murilo, Fornari, Isabella Fernandes, Bernécule, Priscila Neves, Pinheiro, Lara Esquiapatti, Costa, Ricardo Filipe Alves, Longatto-Filho, Adhemar, Junior, João Neif Antonio, Silva, Eduardo Caetano Albino, Cárcano, Flávio Mavignier, Pinheiro, Céline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264765/
https://www.ncbi.nlm.nih.gov/pubmed/34249728
http://dx.doi.org/10.3389/fonc.2021.682665
_version_ 1783719631259697152
author Bonatelli, Murilo
Fornari, Isabella Fernandes
Bernécule, Priscila Neves
Pinheiro, Lara Esquiapatti
Costa, Ricardo Filipe Alves
Longatto-Filho, Adhemar
Junior, João Neif Antonio
Silva, Eduardo Caetano Albino
Cárcano, Flávio Mavignier
Pinheiro, Céline
author_facet Bonatelli, Murilo
Fornari, Isabella Fernandes
Bernécule, Priscila Neves
Pinheiro, Lara Esquiapatti
Costa, Ricardo Filipe Alves
Longatto-Filho, Adhemar
Junior, João Neif Antonio
Silva, Eduardo Caetano Albino
Cárcano, Flávio Mavignier
Pinheiro, Céline
author_sort Bonatelli, Murilo
collection PubMed
description INTRODUCTION: Cancer of unknown primary origin (CUP) is defined as metastatic cancer without identification of the primary site. Considering that only 15–20% of patients with CUP show a favorable outcome, identifying biomarkers may help improve the clinical management of patients who do not respond well to conventional therapies. In this context, the study of the metabolic profile of CUP may pave the way to establish new biomarkers and/or therapeutic targets; therefore, this study aimed to characterize the expression of metabolism-related proteins in CUP. MATERIALS AND METHODS: The expression of monocarboxylate transporters MCT1, MCT2 and MCT4, their chaperone CD147, the glucose transporter GLUT1 and the pH regulator CAIX was evaluated by immunohistochemistry in a series of 118 CUP patients, and the results were associated with the available clinicopathological information. RESULTS: The metabolism-related proteins MCT1, MCT4, CD147, GLUT1 and CAIX were expressed in a critical portion of the CUP (approximately 20 to 70%). MCT1 and CD147 were both more frequently expressed in cases with lymph nodes as metastasis dominant sites (p = 0.001) as well as in samples from lymph nodes (p <0.001 and p = 0.002, respectively), while MCT1 expression was more frequently expressed in squamous cell carcinomas (p = 0.045). A higher overall survival was observed in patients with tumors positive for GLUT1 and CAIX expression (p = 0.011 and p = 0.041, respectively), but none of the proteins was an independent prognostic factor for overall survival in multivariable analysis. CONCLUSION: The results suggest that a portion of CUPs present a hyperglycolytic phenotype, which is associated with higher overall survival.
format Online
Article
Text
id pubmed-8264765
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-82647652021-07-09 Expression of Glycolysis-Related Proteins in Cancer of Unknown Primary Origin Bonatelli, Murilo Fornari, Isabella Fernandes Bernécule, Priscila Neves Pinheiro, Lara Esquiapatti Costa, Ricardo Filipe Alves Longatto-Filho, Adhemar Junior, João Neif Antonio Silva, Eduardo Caetano Albino Cárcano, Flávio Mavignier Pinheiro, Céline Front Oncol Oncology INTRODUCTION: Cancer of unknown primary origin (CUP) is defined as metastatic cancer without identification of the primary site. Considering that only 15–20% of patients with CUP show a favorable outcome, identifying biomarkers may help improve the clinical management of patients who do not respond well to conventional therapies. In this context, the study of the metabolic profile of CUP may pave the way to establish new biomarkers and/or therapeutic targets; therefore, this study aimed to characterize the expression of metabolism-related proteins in CUP. MATERIALS AND METHODS: The expression of monocarboxylate transporters MCT1, MCT2 and MCT4, their chaperone CD147, the glucose transporter GLUT1 and the pH regulator CAIX was evaluated by immunohistochemistry in a series of 118 CUP patients, and the results were associated with the available clinicopathological information. RESULTS: The metabolism-related proteins MCT1, MCT4, CD147, GLUT1 and CAIX were expressed in a critical portion of the CUP (approximately 20 to 70%). MCT1 and CD147 were both more frequently expressed in cases with lymph nodes as metastasis dominant sites (p = 0.001) as well as in samples from lymph nodes (p <0.001 and p = 0.002, respectively), while MCT1 expression was more frequently expressed in squamous cell carcinomas (p = 0.045). A higher overall survival was observed in patients with tumors positive for GLUT1 and CAIX expression (p = 0.011 and p = 0.041, respectively), but none of the proteins was an independent prognostic factor for overall survival in multivariable analysis. CONCLUSION: The results suggest that a portion of CUPs present a hyperglycolytic phenotype, which is associated with higher overall survival. Frontiers Media S.A. 2021-06-24 /pmc/articles/PMC8264765/ /pubmed/34249728 http://dx.doi.org/10.3389/fonc.2021.682665 Text en Copyright © 2021 Bonatelli, Fornari, Bernécule, Pinheiro, Costa, Longatto-Filho, Junior, Silva, Cárcano and Pinheiro https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Bonatelli, Murilo
Fornari, Isabella Fernandes
Bernécule, Priscila Neves
Pinheiro, Lara Esquiapatti
Costa, Ricardo Filipe Alves
Longatto-Filho, Adhemar
Junior, João Neif Antonio
Silva, Eduardo Caetano Albino
Cárcano, Flávio Mavignier
Pinheiro, Céline
Expression of Glycolysis-Related Proteins in Cancer of Unknown Primary Origin
title Expression of Glycolysis-Related Proteins in Cancer of Unknown Primary Origin
title_full Expression of Glycolysis-Related Proteins in Cancer of Unknown Primary Origin
title_fullStr Expression of Glycolysis-Related Proteins in Cancer of Unknown Primary Origin
title_full_unstemmed Expression of Glycolysis-Related Proteins in Cancer of Unknown Primary Origin
title_short Expression of Glycolysis-Related Proteins in Cancer of Unknown Primary Origin
title_sort expression of glycolysis-related proteins in cancer of unknown primary origin
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264765/
https://www.ncbi.nlm.nih.gov/pubmed/34249728
http://dx.doi.org/10.3389/fonc.2021.682665
work_keys_str_mv AT bonatellimurilo expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin
AT fornariisabellafernandes expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin
AT berneculepriscilaneves expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin
AT pinheirolaraesquiapatti expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin
AT costaricardofilipealves expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin
AT longattofilhoadhemar expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin
AT juniorjoaoneifantonio expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin
AT silvaeduardocaetanoalbino expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin
AT carcanoflaviomavignier expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin
AT pinheiroceline expressionofglycolysisrelatedproteinsincancerofunknownprimaryorigin