Associations between persistent organic pollutants and risk of breast cancer metastasis.


Journal

Environment international
ISSN: 1873-6750
Titre abrégé: Environ Int
Pays: Netherlands
ID NLM: 7807270

Informations de publication

Date de publication:
11 2019
Historique:
received: 04 05 2019
revised: 15 07 2019
accepted: 15 07 2019
pubmed: 6 8 2019
medline: 5 3 2020
entrez: 6 8 2019
Statut: ppublish

Résumé

Breast cancer (BC) is a major public health concern with over 2 million new cases diagnosed and over 600,000 deaths in 2018 in women worldwide. When distant metastases are present at diagnosis, the 5-year survival rate is only 26%. Recent studies have suggested that persistent organic pollutants (POPs) that accumulate in adipose tissue (AT) can influence tumor phenotype and stimulate cellular processes important for metastasis such as invasion. We, therefore, tested the hypothesis that POP exposure is associated with BC metastasis. We conducted an exploratory case-control study in which the concentrations of 49 POPs were measured in both AT and serum samples from BC patients, with or without lymph node metastasis, who underwent partial or total mastectomies, lymph node biopsies and sampling of the adipocytic tumor microenvironment. Adjusted, unconditional logistic models were used to study the associations between the POP concentrations and the risk of metastasis and other hallmarks of cancer aggressiveness. 2.3.7.8-TCDD concentrations in AT are positively associated with the risk of metastasis in 43 patients who have BMIs equal or higher than 25 kg/m2 (odds ratio: 4.48 (1.32-20.71)). Furthermore, the concentrations of 2.3.7.8-TCDD and two coplanar PCBs (77&169) in AT also were positively associated with the risk of lymph node metastasis and the tumor size. Our study suggests that 2.3.7.8-TCDD and some PCBs contribute to the development of tumor metastasis and other hallmarks of cancer aggressiveness. While these results should be considered with caution, this is the first study to identify such potential risk factors. Larger longitudinal studies are necessary to confirm our results. Clinical Trial Protocol Record: 2013-A00663-42.

Sections du résumé

BACKGROUND
Breast cancer (BC) is a major public health concern with over 2 million new cases diagnosed and over 600,000 deaths in 2018 in women worldwide. When distant metastases are present at diagnosis, the 5-year survival rate is only 26%. Recent studies have suggested that persistent organic pollutants (POPs) that accumulate in adipose tissue (AT) can influence tumor phenotype and stimulate cellular processes important for metastasis such as invasion. We, therefore, tested the hypothesis that POP exposure is associated with BC metastasis.
METHODS
We conducted an exploratory case-control study in which the concentrations of 49 POPs were measured in both AT and serum samples from BC patients, with or without lymph node metastasis, who underwent partial or total mastectomies, lymph node biopsies and sampling of the adipocytic tumor microenvironment. Adjusted, unconditional logistic models were used to study the associations between the POP concentrations and the risk of metastasis and other hallmarks of cancer aggressiveness.
RESULTS
2.3.7.8-TCDD concentrations in AT are positively associated with the risk of metastasis in 43 patients who have BMIs equal or higher than 25 kg/m2 (odds ratio: 4.48 (1.32-20.71)). Furthermore, the concentrations of 2.3.7.8-TCDD and two coplanar PCBs (77&169) in AT also were positively associated with the risk of lymph node metastasis and the tumor size.
CONCLUSION
Our study suggests that 2.3.7.8-TCDD and some PCBs contribute to the development of tumor metastasis and other hallmarks of cancer aggressiveness. While these results should be considered with caution, this is the first study to identify such potential risk factors. Larger longitudinal studies are necessary to confirm our results. Clinical Trial Protocol Record: 2013-A00663-42.

Identifiants

pubmed: 31382183
pii: S0160-4120(19)31495-3
doi: 10.1016/j.envint.2019.105028
pii:
doi:

Substances chimiques

Environmental Pollutants 0
Polychlorinated Biphenyls DFC2HB4I0K

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

105028

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Meriem Koual (M)

INSERM UMR-S 1124, 45 rue des Saints-Pères, 75006 Paris, France; Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Service de Chirurgie Cancérologique Gynécologique et du Sein, Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

German Cano-Sancho (G)

LABERCA, Oniris, INRA, Université Bretagne-Loire, 44307 Nantes, France.

Anne-Sophie Bats (AS)

INSERM UMR-S 1124, 45 rue des Saints-Pères, 75006 Paris, France; Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Service de Chirurgie Cancérologique Gynécologique et du Sein, Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

Céline Tomkiewicz (C)

INSERM UMR-S 1124, 45 rue des Saints-Pères, 75006 Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

Yael Kaddouch-Amar (Y)

INSERM UMR-S 1124, 45 rue des Saints-Pères, 75006 Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

Nathalie Douay-Hauser (N)

INSERM UMR-S 1124, 45 rue des Saints-Pères, 75006 Paris, France; Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Service de Chirurgie Cancérologique Gynécologique et du Sein, Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

Charlotte Ngo (C)

Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Service de Chirurgie Cancérologique Gynécologique et du Sein, Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

Hélène Bonsang (H)

Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Service de Chirurgie Cancérologique Gynécologique et du Sein, Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

Myriam Deloménie (M)

Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Service de Chirurgie Cancérologique Gynécologique et du Sein, Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

Fabrice Lecuru (F)

INSERM UMR-S 1124, 45 rue des Saints-Pères, 75006 Paris, France; Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Service de Chirurgie Cancérologique Gynécologique et du Sein, Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

Bruno Le Bizec (B)

LABERCA, Oniris, INRA, Université Bretagne-Loire, 44307 Nantes, France.

Philippe Marchand (P)

LABERCA, Oniris, INRA, Université Bretagne-Loire, 44307 Nantes, France.

Jeremie Botton (J)

Faculty of Pharmacy, Univ. Paris-Sud, Université Paris-Saclay, F-92296 Châtenay-Malabry, France.

Robert Barouki (R)

INSERM UMR-S 1124, 45 rue des Saints-Pères, 75006 Paris, France; Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Service de Chirurgie Cancérologique Gynécologique et du Sein, Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France.

Jean-Philippe Antignac (JP)

LABERCA, Oniris, INRA, Université Bretagne-Loire, 44307 Nantes, France.

Xavier Coumoul (X)

INSERM UMR-S 1124, 45 rue des Saints-Pères, 75006 Paris, France; Université de Paris, 45 rue des Saints-Pères, 75006 Paris, France. Electronic address: xavier.coumoul@parisdescartes.fr.

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Classifications MeSH