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Adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing CCL5
Growing evidence indicates that adiposity is associated with raised cancer incidence, morbidity and mortality. In a subset of tumors, cancer cell growth and/or metastasis predominantly occur in adipocyte-rich microenvironment. Indeed, adipocytes represent the most abundant cell types surrounding bre...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029717/ https://www.ncbi.nlm.nih.gov/pubmed/27027351 http://dx.doi.org/10.18632/oncotarget.8336 |
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author | D’Esposito, Vittoria Liguoro, Domenico Ambrosio, Maria Rosaria Collina, Francesca Cantile, Monica Spinelli, Rosa Raciti, Gregory Alexander Miele, Claudia Valentino, Rossella Campiglia, Pietro De Laurentiis, Michelino Di Bonito, Maurizio Botti, Gerardo Franco, Renato Beguinot, Francesco Formisano, Pietro |
author_facet | D’Esposito, Vittoria Liguoro, Domenico Ambrosio, Maria Rosaria Collina, Francesca Cantile, Monica Spinelli, Rosa Raciti, Gregory Alexander Miele, Claudia Valentino, Rossella Campiglia, Pietro De Laurentiis, Michelino Di Bonito, Maurizio Botti, Gerardo Franco, Renato Beguinot, Francesco Formisano, Pietro |
author_sort | D’Esposito, Vittoria |
collection | PubMed |
description | Growing evidence indicates that adiposity is associated with raised cancer incidence, morbidity and mortality. In a subset of tumors, cancer cell growth and/or metastasis predominantly occur in adipocyte-rich microenvironment. Indeed, adipocytes represent the most abundant cell types surrounding breast cancer cells. We have studied the mechanisms by which peritumoral human adipose tissue contributes to Triple Negative Breast Cancer (TNBC) cell invasiveness and dissemination. Co-culture with human adipocytes enhanced MDA-MB231 cancer cell invasiveness. Adipocytes cultured in high glucose were 2-fold more active in promoting cell invasion and motility compared to those cultured in low glucose. This effect is induced, at least in part, by the CC-chemokine ligand 5 (CCL5). Indeed, CCL5 inhibition by specific peptides and antibodies reduced adipocyte-induced breast cancer cell migration and invasion. CCL5 immuno-detection in peritumoral adipose tissue of women with TNBC correlated with lymph node (p-value = 0.04) and distant metastases (p-value = 0.001). A positive trend was also observed between CCL5 expression and glycaemia. Finally, Kaplan-Meier curves showed a negative correlation between CCL5 staining in the peritumoral adipose tissue and overall survival of patients (p-value = 0.039). Thus, inhibition of CCL5 in adipose microenvironment may represent a novel approach for the therapy of highly malignant TNBC. |
format | Online Article Text |
id | pubmed-5029717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50297172016-09-29 Adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing CCL5 D’Esposito, Vittoria Liguoro, Domenico Ambrosio, Maria Rosaria Collina, Francesca Cantile, Monica Spinelli, Rosa Raciti, Gregory Alexander Miele, Claudia Valentino, Rossella Campiglia, Pietro De Laurentiis, Michelino Di Bonito, Maurizio Botti, Gerardo Franco, Renato Beguinot, Francesco Formisano, Pietro Oncotarget Research Paper Growing evidence indicates that adiposity is associated with raised cancer incidence, morbidity and mortality. In a subset of tumors, cancer cell growth and/or metastasis predominantly occur in adipocyte-rich microenvironment. Indeed, adipocytes represent the most abundant cell types surrounding breast cancer cells. We have studied the mechanisms by which peritumoral human adipose tissue contributes to Triple Negative Breast Cancer (TNBC) cell invasiveness and dissemination. Co-culture with human adipocytes enhanced MDA-MB231 cancer cell invasiveness. Adipocytes cultured in high glucose were 2-fold more active in promoting cell invasion and motility compared to those cultured in low glucose. This effect is induced, at least in part, by the CC-chemokine ligand 5 (CCL5). Indeed, CCL5 inhibition by specific peptides and antibodies reduced adipocyte-induced breast cancer cell migration and invasion. CCL5 immuno-detection in peritumoral adipose tissue of women with TNBC correlated with lymph node (p-value = 0.04) and distant metastases (p-value = 0.001). A positive trend was also observed between CCL5 expression and glycaemia. Finally, Kaplan-Meier curves showed a negative correlation between CCL5 staining in the peritumoral adipose tissue and overall survival of patients (p-value = 0.039). Thus, inhibition of CCL5 in adipose microenvironment may represent a novel approach for the therapy of highly malignant TNBC. Impact Journals LLC 2016-03-24 /pmc/articles/PMC5029717/ /pubmed/27027351 http://dx.doi.org/10.18632/oncotarget.8336 Text en Copyright: © 2016 D’Esposito et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper D’Esposito, Vittoria Liguoro, Domenico Ambrosio, Maria Rosaria Collina, Francesca Cantile, Monica Spinelli, Rosa Raciti, Gregory Alexander Miele, Claudia Valentino, Rossella Campiglia, Pietro De Laurentiis, Michelino Di Bonito, Maurizio Botti, Gerardo Franco, Renato Beguinot, Francesco Formisano, Pietro Adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing CCL5 |
title | Adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing CCL5 |
title_full | Adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing CCL5 |
title_fullStr | Adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing CCL5 |
title_full_unstemmed | Adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing CCL5 |
title_short | Adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing CCL5 |
title_sort | adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing ccl5 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029717/ https://www.ncbi.nlm.nih.gov/pubmed/27027351 http://dx.doi.org/10.18632/oncotarget.8336 |
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