Asthma-related inflammation promotes lung metastasis of breast cancer cells through CCL11-CCR3 pathway.


Journal

Respiratory research
ISSN: 1465-993X
Titre abrégé: Respir Res
Pays: England
ID NLM: 101090633

Informations de publication

Date de publication:
19 Feb 2021
Historique:
received: 29 10 2020
accepted: 07 02 2021
entrez: 20 2 2021
pubmed: 21 2 2021
medline: 5 11 2021
Statut: epublish

Résumé

Mechanisms that preclude lung metastasis are still barely understood. The possible consequences of allergic airways inflammation on cancer dissemination were studied in a mouse model of breast cancer. Balb/c mice were immunized and daily exposed to ovalbumin (OVA) from day 21. They were subcutaneously injected with 4T1 mammary tumor cells on day 45 and sacrificed on day 67. Lung metastases were measured by biophotonic imaging (IVIS® 200 Imaging System) and histological measurement of tumor area (Cytomine software). Effects of CCL11 were assessed in vivo by intratracheal instillations of recCCL11 and in vitro using Boyden chambers. CCR3 expression on cell surface was assessed by flow cytometry. The extent of tumor metastases was significantly higher in lungs of OVA-exposed mice and increased levels of CCL11 expression were measured after OVA exposure. Migration of 4T1 cells and neutrophils was stimulated in vitro and in vivo by recCCL11. 4T1 cells and neutrophils express CCR3 as shown by flow cytometry and a selective CCR3 antagonist (SB-297006) inhibited the induction of 4T1 cells migration and proliferation in response to recCCL11. Allergic inflammation generated by exposure to allergens triggers the implantation of metastatic cells from primary breast tumor into lung tissues plausibly in a CCL11-CCR3-dependent manner. This indicates that asthma related inflammation in lungs might be a risk factor for lung metastasis in breast cancer patients.

Sections du résumé

BACKGROUND BACKGROUND
Mechanisms that preclude lung metastasis are still barely understood. The possible consequences of allergic airways inflammation on cancer dissemination were studied in a mouse model of breast cancer.
METHODS METHODS
Balb/c mice were immunized and daily exposed to ovalbumin (OVA) from day 21. They were subcutaneously injected with 4T1 mammary tumor cells on day 45 and sacrificed on day 67. Lung metastases were measured by biophotonic imaging (IVIS® 200 Imaging System) and histological measurement of tumor area (Cytomine software). Effects of CCL11 were assessed in vivo by intratracheal instillations of recCCL11 and in vitro using Boyden chambers. CCR3 expression on cell surface was assessed by flow cytometry.
RESULTS RESULTS
The extent of tumor metastases was significantly higher in lungs of OVA-exposed mice and increased levels of CCL11 expression were measured after OVA exposure. Migration of 4T1 cells and neutrophils was stimulated in vitro and in vivo by recCCL11. 4T1 cells and neutrophils express CCR3 as shown by flow cytometry and a selective CCR3 antagonist (SB-297006) inhibited the induction of 4T1 cells migration and proliferation in response to recCCL11.
CONCLUSIONS CONCLUSIONS
Allergic inflammation generated by exposure to allergens triggers the implantation of metastatic cells from primary breast tumor into lung tissues plausibly in a CCL11-CCR3-dependent manner. This indicates that asthma related inflammation in lungs might be a risk factor for lung metastasis in breast cancer patients.

Identifiants

pubmed: 33608009
doi: 10.1186/s12931-021-01652-9
pii: 10.1186/s12931-021-01652-9
pmc: PMC7893955
doi:

Substances chimiques

Ccl11 protein, mouse 0
Ccr3 protein, mouse 0
Chemokine CCL11 0
Receptors, CCR3 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

61

Subventions

Organisme : Fonds De La Recherche Scientifique - FNRS
ID : 7463012F

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Auteurs

S Bekaert (S)

Laboratory of Tumor and Development Biology, GIGA-Cancer - University of Liege and CHU Liege, 4000, Liege, Belgium.

N Rocks (N)

Laboratory of Tumor and Development Biology, GIGA-Cancer - University of Liege and CHU Liege, 4000, Liege, Belgium.

C Vanwinge (C)

Laboratory of Tumor and Development Biology, GIGA-Cancer - University of Liege and CHU Liege, 4000, Liege, Belgium.

A Noel (A)

Laboratory of Tumor and Development Biology, GIGA-Cancer - University of Liege and CHU Liege, 4000, Liege, Belgium.

D Cataldo (D)

Laboratory of Tumor and Development Biology, GIGA-Cancer - University of Liege and CHU Liege, 4000, Liege, Belgium. didier.cataldo@uliege.be.
University of Liege, Tower of Pathology (B23), 3rd Floor, 4000, Liege, Belgium. didier.cataldo@uliege.be.

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Classifications MeSH