Aggressiveness and Metastatic Potential of Breast Cancer Cells Co-Cultured with Preadipocytes and Exposed to an Environmental Pollutant Dioxin: An


Journal

Environmental health perspectives
ISSN: 1552-9924
Titre abrégé: Environ Health Perspect
Pays: United States
ID NLM: 0330411

Informations de publication

Date de publication:
03 2021
Historique:
entrez: 8 3 2021
pubmed: 9 3 2021
medline: 26 11 2021
Statut: ppublish

Résumé

Breast cancer (BC) is a major public health concern, and its prognosis is very poor once metastasis occurs. The tumor microenvironment and chemical pollution have been suggested recently to contribute, independently, to the development of metastatic cells. The BC microenvironment consists, in part, of adipocytes and preadipocytes in which persistent organic pollutants (POPs) can be stored. We aimed to test the hypothesis that these two factors (2,3,7,8-tetrachlorodibenzo- We used a co-culture model using BC MCF-7 cells or MDA-MB-231 cells together with hMADS preadipocytes to investigate the contribution of the microenvironment and 2,3,7,8-tetrachlorodibenzo- We found that coexposure to TCDD and preadipocytes modified BC cell properties; moreover, it induced the expression of ALDH1A3, a cancer stem cell marker, and the appearance of giant cancer cells with cell-in-cell structures (CICs), which are associated with malignant metastatic progression, that we demonstrated The results of our study using BC cell lines co-cultured with preadipocytes and a POP and an

Sections du résumé

BACKGROUND
Breast cancer (BC) is a major public health concern, and its prognosis is very poor once metastasis occurs. The tumor microenvironment and chemical pollution have been suggested recently to contribute, independently, to the development of metastatic cells. The BC microenvironment consists, in part, of adipocytes and preadipocytes in which persistent organic pollutants (POPs) can be stored.
OBJECTIVES
We aimed to test the hypothesis that these two factors (2,3,7,8-tetrachlorodibenzo-
METHODS
We used a co-culture model using BC MCF-7 cells or MDA-MB-231 cells together with hMADS preadipocytes to investigate the contribution of the microenvironment and 2,3,7,8-tetrachlorodibenzo-
RESULTS
We found that coexposure to TCDD and preadipocytes modified BC cell properties; moreover, it induced the expression of ALDH1A3, a cancer stem cell marker, and the appearance of giant cancer cells with cell-in-cell structures (CICs), which are associated with malignant metastatic progression, that we demonstrated
DISCUSSION
The results of our study using BC cell lines co-cultured with preadipocytes and a POP and an

Identifiants

pubmed: 33683140
doi: 10.1289/EHP7102
pmc: PMC7939125
doi:

Substances chimiques

Dioxins 0
Environmental Pollutants 0
Polychlorinated Dibenzodioxins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

37002

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Auteurs

Meriem Koual (M)

UMR-S1124, Institut national de la santé et de la recherché médicale (Inserm), T3S, Toxicologie Environnementale, Cibles thérapeutiques, Signalisation cellulaire et Biomarqueurs, Paris, France.
Service de Chirurgie Cancérologique Gynécologique et du Sein, Hôpital Européen Georges-Pompidou, Assistance Publique-Hôpitaux de Paris, France.
Université de Paris, Paris, France.

Céline Tomkiewicz (C)

UMR-S1124, Institut national de la santé et de la recherché médicale (Inserm), T3S, Toxicologie Environnementale, Cibles thérapeutiques, Signalisation cellulaire et Biomarqueurs, Paris, France.

Ida Chiara Guerrera (IC)

Plateforme protéomique 3P5-Necker, Structure Fédérative de Recherche Necker, Université de Paris, US24/CNRS UMS3633, Inserm, Paris, France.

David Sherr (D)

Department of Environmental Health, Boston University School of Public Health, Boston, Massachusetts, USA.

Robert Barouki (R)

UMR-S1124, Institut national de la santé et de la recherché médicale (Inserm), T3S, Toxicologie Environnementale, Cibles thérapeutiques, Signalisation cellulaire et Biomarqueurs, Paris, France.
Université de Paris, Paris, France.

Xavier Coumoul (X)

UMR-S1124, Institut national de la santé et de la recherché médicale (Inserm), T3S, Toxicologie Environnementale, Cibles thérapeutiques, Signalisation cellulaire et Biomarqueurs, Paris, France.
Université de Paris, Paris, France.

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