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Adenosine Stimulate Proliferation and Migration in Triple Negative Breast Cancer Cells

Emerging evidence suggests that the adenosine (Ado) receptors may play crucial roles in tumor progression. Here, we show that Ado increases proliferation and migration in a triple negative breast cancer model, the MDA-MB 231 cell line. The use of specific agonists and antagonists evidenced that thes...

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Autores principales: Fernandez-Gallardo, Miriam, González-Ramírez, Ricardo, Sandoval, Alejandro, Felix, Ricardo, Monjaraz, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135100/
https://www.ncbi.nlm.nih.gov/pubmed/27911956
http://dx.doi.org/10.1371/journal.pone.0167445
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author Fernandez-Gallardo, Miriam
González-Ramírez, Ricardo
Sandoval, Alejandro
Felix, Ricardo
Monjaraz, Eduardo
author_facet Fernandez-Gallardo, Miriam
González-Ramírez, Ricardo
Sandoval, Alejandro
Felix, Ricardo
Monjaraz, Eduardo
author_sort Fernandez-Gallardo, Miriam
collection PubMed
description Emerging evidence suggests that the adenosine (Ado) receptors may play crucial roles in tumor progression. Here, we show that Ado increases proliferation and migration in a triple negative breast cancer model, the MDA-MB 231 cell line. The use of specific agonists and antagonists evidenced that these effects depend on the activation of the A(2B) receptor, which then triggers an intracellular response mediated by the adenylate cyclase/PKA/cAMP signaling pathway. Ado also increases the expression of Na(V)1.5 channels, a potential biomarker in breast cancer. Together, these data suggest important roles of the A(2B) receptors and Na(V)1.5 channels in the Ado-induced increase in proliferation and migration of the MDA-MB 231 cells.
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spelling pubmed-51351002016-12-21 Adenosine Stimulate Proliferation and Migration in Triple Negative Breast Cancer Cells Fernandez-Gallardo, Miriam González-Ramírez, Ricardo Sandoval, Alejandro Felix, Ricardo Monjaraz, Eduardo PLoS One Research Article Emerging evidence suggests that the adenosine (Ado) receptors may play crucial roles in tumor progression. Here, we show that Ado increases proliferation and migration in a triple negative breast cancer model, the MDA-MB 231 cell line. The use of specific agonists and antagonists evidenced that these effects depend on the activation of the A(2B) receptor, which then triggers an intracellular response mediated by the adenylate cyclase/PKA/cAMP signaling pathway. Ado also increases the expression of Na(V)1.5 channels, a potential biomarker in breast cancer. Together, these data suggest important roles of the A(2B) receptors and Na(V)1.5 channels in the Ado-induced increase in proliferation and migration of the MDA-MB 231 cells. Public Library of Science 2016-12-02 /pmc/articles/PMC5135100/ /pubmed/27911956 http://dx.doi.org/10.1371/journal.pone.0167445 Text en © 2016 Fernandez-Gallardo et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fernandez-Gallardo, Miriam
González-Ramírez, Ricardo
Sandoval, Alejandro
Felix, Ricardo
Monjaraz, Eduardo
Adenosine Stimulate Proliferation and Migration in Triple Negative Breast Cancer Cells
title Adenosine Stimulate Proliferation and Migration in Triple Negative Breast Cancer Cells
title_full Adenosine Stimulate Proliferation and Migration in Triple Negative Breast Cancer Cells
title_fullStr Adenosine Stimulate Proliferation and Migration in Triple Negative Breast Cancer Cells
title_full_unstemmed Adenosine Stimulate Proliferation and Migration in Triple Negative Breast Cancer Cells
title_short Adenosine Stimulate Proliferation and Migration in Triple Negative Breast Cancer Cells
title_sort adenosine stimulate proliferation and migration in triple negative breast cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135100/
https://www.ncbi.nlm.nih.gov/pubmed/27911956
http://dx.doi.org/10.1371/journal.pone.0167445
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