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Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells
Type 2 diabetes and obesity are negative prognostic factors in patients with breast cancer (BC). We found that sensitivity to tamoxifen was reduced by 2-fold by 25 mM glucose (High Glucose; HG) compared to 5.5 mM glucose (Low Glucose; LG) in MCF7 BC cells. Shifting from HG to LG ameliorated MCF7 cel...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752499/ https://www.ncbi.nlm.nih.gov/pubmed/29312586 http://dx.doi.org/10.18632/oncotarget.22552 |
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author | Ambrosio, Maria Rosaria D’Esposito, Vittoria Costa, Valerio Liguoro, Domenico Collina, Francesca Cantile, Monica Prevete, Nella Passaro, Carmela Mosca, Giusy De Laurentiis, Michelino Di Bonito, Maurizio Botti, Gerardo Franco, Renato Beguinot, Francesco Ciccodicola, Alfredo Formisano, Pietro |
author_facet | Ambrosio, Maria Rosaria D’Esposito, Vittoria Costa, Valerio Liguoro, Domenico Collina, Francesca Cantile, Monica Prevete, Nella Passaro, Carmela Mosca, Giusy De Laurentiis, Michelino Di Bonito, Maurizio Botti, Gerardo Franco, Renato Beguinot, Francesco Ciccodicola, Alfredo Formisano, Pietro |
author_sort | Ambrosio, Maria Rosaria |
collection | PubMed |
description | Type 2 diabetes and obesity are negative prognostic factors in patients with breast cancer (BC). We found that sensitivity to tamoxifen was reduced by 2-fold by 25 mM glucose (High Glucose; HG) compared to 5.5 mM glucose (Low Glucose; LG) in MCF7 BC cells. Shifting from HG to LG ameliorated MCF7 cell responsiveness to tamoxifen. RNA-Sequencing of MCF7 BC cells revealed that cell cycle-related genes were mainly affected by glucose. Connective Tissue Growth Factor (CTGF) was identified as a glucose-induced modulator of cell sensitivity to tamoxifen. Co-culturing MCF7 cells with human adipocytes exposed to HG, enhanced CTGF mRNA levels and reduced tamoxifen responsiveness of BC cells. Inhibition of adipocyte-released IL8 reverted these effects. Interestingly, CTGF immuno-detection in bioptic specimens from women with estrogen receptor positive (ER(+)) BC correlated with hormone therapy resistance, distant metastases, reduced overall and disease-free survival. Thus, glucose affects tamoxifen responsiveness directly modulating CTGF in BC cells, and indirectly promoting IL8 release by adipocytes. |
format | Online Article Text |
id | pubmed-5752499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57524992018-01-08 Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells Ambrosio, Maria Rosaria D’Esposito, Vittoria Costa, Valerio Liguoro, Domenico Collina, Francesca Cantile, Monica Prevete, Nella Passaro, Carmela Mosca, Giusy De Laurentiis, Michelino Di Bonito, Maurizio Botti, Gerardo Franco, Renato Beguinot, Francesco Ciccodicola, Alfredo Formisano, Pietro Oncotarget Research Paper Type 2 diabetes and obesity are negative prognostic factors in patients with breast cancer (BC). We found that sensitivity to tamoxifen was reduced by 2-fold by 25 mM glucose (High Glucose; HG) compared to 5.5 mM glucose (Low Glucose; LG) in MCF7 BC cells. Shifting from HG to LG ameliorated MCF7 cell responsiveness to tamoxifen. RNA-Sequencing of MCF7 BC cells revealed that cell cycle-related genes were mainly affected by glucose. Connective Tissue Growth Factor (CTGF) was identified as a glucose-induced modulator of cell sensitivity to tamoxifen. Co-culturing MCF7 cells with human adipocytes exposed to HG, enhanced CTGF mRNA levels and reduced tamoxifen responsiveness of BC cells. Inhibition of adipocyte-released IL8 reverted these effects. Interestingly, CTGF immuno-detection in bioptic specimens from women with estrogen receptor positive (ER(+)) BC correlated with hormone therapy resistance, distant metastases, reduced overall and disease-free survival. Thus, glucose affects tamoxifen responsiveness directly modulating CTGF in BC cells, and indirectly promoting IL8 release by adipocytes. Impact Journals LLC 2017-11-20 /pmc/articles/PMC5752499/ /pubmed/29312586 http://dx.doi.org/10.18632/oncotarget.22552 Text en Copyright: © 2017 Ambrosio et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Ambrosio, Maria Rosaria D’Esposito, Vittoria Costa, Valerio Liguoro, Domenico Collina, Francesca Cantile, Monica Prevete, Nella Passaro, Carmela Mosca, Giusy De Laurentiis, Michelino Di Bonito, Maurizio Botti, Gerardo Franco, Renato Beguinot, Francesco Ciccodicola, Alfredo Formisano, Pietro Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells |
title | Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells |
title_full | Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells |
title_fullStr | Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells |
title_full_unstemmed | Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells |
title_short | Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells |
title_sort | glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752499/ https://www.ncbi.nlm.nih.gov/pubmed/29312586 http://dx.doi.org/10.18632/oncotarget.22552 |
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