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Long-Term Exposure of Early-Transformed Human Mammary Cells to Low Doses of Benzo[a]pyrene and/or Bisphenol A Enhances Their Cancerous Phenotype via an AhR/GPR30 Interplay

It is of utmost importance to decipher the role of chronic exposure to low doses of environmental carcinogens on breast cancer progression. The early-transformed triple-negative human mammary MCF10AT1 cells were chronically (60 days) exposed to low doses (10(−10) M) of Benzo[a]pyrene (B[a]P), a geno...

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Autores principales: Donini, Caterina F., El Helou, Myriam, Wierinckx, Anne, Győrffy, Balázs, Aires, Sophie, Escande, Aurélie, Croze, Séverine, Clezardin, Philippe, Lachuer, Joël, Diab-Assaf, Mona, Ghayad, Sandra E., Fervers, Béatrice, Cavaillès, Vincent, Maguer-Satta, Véronique, Cohen, Pascale A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326103/
https://www.ncbi.nlm.nih.gov/pubmed/32670863
http://dx.doi.org/10.3389/fonc.2020.00712
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author Donini, Caterina F.
El Helou, Myriam
Wierinckx, Anne
Győrffy, Balázs
Aires, Sophie
Escande, Aurélie
Croze, Séverine
Clezardin, Philippe
Lachuer, Joël
Diab-Assaf, Mona
Ghayad, Sandra E.
Fervers, Béatrice
Cavaillès, Vincent
Maguer-Satta, Véronique
Cohen, Pascale A.
author_facet Donini, Caterina F.
El Helou, Myriam
Wierinckx, Anne
Győrffy, Balázs
Aires, Sophie
Escande, Aurélie
Croze, Séverine
Clezardin, Philippe
Lachuer, Joël
Diab-Assaf, Mona
Ghayad, Sandra E.
Fervers, Béatrice
Cavaillès, Vincent
Maguer-Satta, Véronique
Cohen, Pascale A.
author_sort Donini, Caterina F.
collection PubMed
description It is of utmost importance to decipher the role of chronic exposure to low doses of environmental carcinogens on breast cancer progression. The early-transformed triple-negative human mammary MCF10AT1 cells were chronically (60 days) exposed to low doses (10(−10) M) of Benzo[a]pyrene (B[a]P), a genotoxic agent, and/or Bisphenol A (BPA), an endocrine disruptor. Our study revealed that exposed MCF10AT1 cells developed, in a time-dependent manner, an acquired phenotype characterized by an increase in cancerous properties (anchorage independent growth and stem-like phenotype). Co-exposure of MCF10AT1 cells to B[a]P and BPA led to a significantly greater aggressive phenotype compared to B[a]P or BPA alone. This study provided new insights into the existence of a functional interplay between the aryl hydrocarbon receptor (AhR) and the G protein-coupled receptor 30 (GPR30) by which chronic and low-dose exposure of B[a]P and/or BPA fosters the progression of MCF10AT1 cells into a more aggressive substage. Experiments using AhR or GPR30 antagonists, siRNA strategies, and RNAseq analysis led us to propose a model in which AhR signaling plays a “driver role” in the AhR/GPR30 cross-talk in mediating long-term and low-dose exposure of B[a]P and/or BPA. Retrospective analysis of two independent breast cancer cohorts revealed that the AhR/GPR30 mRNA expression signature resulted in poor breast cancer prognosis, in particular in the ER-negative and the triple-negative subtypes. Finally, the study identified targeting AhR and/or GPR30 with specific antagonists as a strategy capable of inhibiting carcinogenesis associated with chronic exposure to low doses of B[a]P and BPA in MCF10AT1 cells. Altogether, our results indicate that the engagement of both AhR and GPR30 functions, in particular in an ER-negative/triple-negative context of breast cells, favors tumor progression and leads to poor prognosis.
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spelling pubmed-73261032020-07-14 Long-Term Exposure of Early-Transformed Human Mammary Cells to Low Doses of Benzo[a]pyrene and/or Bisphenol A Enhances Their Cancerous Phenotype via an AhR/GPR30 Interplay Donini, Caterina F. El Helou, Myriam Wierinckx, Anne Győrffy, Balázs Aires, Sophie Escande, Aurélie Croze, Séverine Clezardin, Philippe Lachuer, Joël Diab-Assaf, Mona Ghayad, Sandra E. Fervers, Béatrice Cavaillès, Vincent Maguer-Satta, Véronique Cohen, Pascale A. Front Oncol Oncology It is of utmost importance to decipher the role of chronic exposure to low doses of environmental carcinogens on breast cancer progression. The early-transformed triple-negative human mammary MCF10AT1 cells were chronically (60 days) exposed to low doses (10(−10) M) of Benzo[a]pyrene (B[a]P), a genotoxic agent, and/or Bisphenol A (BPA), an endocrine disruptor. Our study revealed that exposed MCF10AT1 cells developed, in a time-dependent manner, an acquired phenotype characterized by an increase in cancerous properties (anchorage independent growth and stem-like phenotype). Co-exposure of MCF10AT1 cells to B[a]P and BPA led to a significantly greater aggressive phenotype compared to B[a]P or BPA alone. This study provided new insights into the existence of a functional interplay between the aryl hydrocarbon receptor (AhR) and the G protein-coupled receptor 30 (GPR30) by which chronic and low-dose exposure of B[a]P and/or BPA fosters the progression of MCF10AT1 cells into a more aggressive substage. Experiments using AhR or GPR30 antagonists, siRNA strategies, and RNAseq analysis led us to propose a model in which AhR signaling plays a “driver role” in the AhR/GPR30 cross-talk in mediating long-term and low-dose exposure of B[a]P and/or BPA. Retrospective analysis of two independent breast cancer cohorts revealed that the AhR/GPR30 mRNA expression signature resulted in poor breast cancer prognosis, in particular in the ER-negative and the triple-negative subtypes. Finally, the study identified targeting AhR and/or GPR30 with specific antagonists as a strategy capable of inhibiting carcinogenesis associated with chronic exposure to low doses of B[a]P and BPA in MCF10AT1 cells. Altogether, our results indicate that the engagement of both AhR and GPR30 functions, in particular in an ER-negative/triple-negative context of breast cells, favors tumor progression and leads to poor prognosis. Frontiers Media S.A. 2020-05-29 /pmc/articles/PMC7326103/ /pubmed/32670863 http://dx.doi.org/10.3389/fonc.2020.00712 Text en Copyright © 2020 Donini, El Helou, Wierinckx, Győrffy, Aires, Escande, Croze, Clezardin, Lachuer, Diab-Assaf, Ghayad, Fervers, Cavaillès, Maguer-Satta and Cohen. http://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
Donini, Caterina F.
El Helou, Myriam
Wierinckx, Anne
Győrffy, Balázs
Aires, Sophie
Escande, Aurélie
Croze, Séverine
Clezardin, Philippe
Lachuer, Joël
Diab-Assaf, Mona
Ghayad, Sandra E.
Fervers, Béatrice
Cavaillès, Vincent
Maguer-Satta, Véronique
Cohen, Pascale A.
Long-Term Exposure of Early-Transformed Human Mammary Cells to Low Doses of Benzo[a]pyrene and/or Bisphenol A Enhances Their Cancerous Phenotype via an AhR/GPR30 Interplay
title Long-Term Exposure of Early-Transformed Human Mammary Cells to Low Doses of Benzo[a]pyrene and/or Bisphenol A Enhances Their Cancerous Phenotype via an AhR/GPR30 Interplay
title_full Long-Term Exposure of Early-Transformed Human Mammary Cells to Low Doses of Benzo[a]pyrene and/or Bisphenol A Enhances Their Cancerous Phenotype via an AhR/GPR30 Interplay
title_fullStr Long-Term Exposure of Early-Transformed Human Mammary Cells to Low Doses of Benzo[a]pyrene and/or Bisphenol A Enhances Their Cancerous Phenotype via an AhR/GPR30 Interplay
title_full_unstemmed Long-Term Exposure of Early-Transformed Human Mammary Cells to Low Doses of Benzo[a]pyrene and/or Bisphenol A Enhances Their Cancerous Phenotype via an AhR/GPR30 Interplay
title_short Long-Term Exposure of Early-Transformed Human Mammary Cells to Low Doses of Benzo[a]pyrene and/or Bisphenol A Enhances Their Cancerous Phenotype via an AhR/GPR30 Interplay
title_sort long-term exposure of early-transformed human mammary cells to low doses of benzo[a]pyrene and/or bisphenol a enhances their cancerous phenotype via an ahr/gpr30 interplay
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326103/
https://www.ncbi.nlm.nih.gov/pubmed/32670863
http://dx.doi.org/10.3389/fonc.2020.00712
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