Immunomodulatory role of histamine H4 receptor in breast cancer.


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
01 2019
Historique:
received: 20 03 2018
accepted: 12 06 2018
revised: 08 06 2018
pubmed: 11 7 2018
medline: 19 9 2019
entrez: 11 7 2018
Statut: ppublish

Résumé

Although the role of histamine H4 receptor (H4R) in immune cells is being extensively investigated, its immunomodulatory function in cancer is completely unknown. This study aimed to investigate the role of H4R in antitumour immunity in a model of triple-negative breast cancer. We evaluated growth parameters, histological characteristics and the composition of tumour, splenic and tumour draining lymph node (TDLN) immune subsets, in a syngeneic model, developed orthotopically with 4T1 cells in H4R knockout (H4R-KO) and wild-type mice. Mice lacking H4R show reduced tumour size and weight, decreased number of lung metastases and percentage of CD4 This is the first report that demonstrates the participation of H4R in antitumour immunity, suggesting that H4R could be a target for cancer treatment.

Sections du résumé

BACKGROUND
Although the role of histamine H4 receptor (H4R) in immune cells is being extensively investigated, its immunomodulatory function in cancer is completely unknown. This study aimed to investigate the role of H4R in antitumour immunity in a model of triple-negative breast cancer.
METHODS
We evaluated growth parameters, histological characteristics and the composition of tumour, splenic and tumour draining lymph node (TDLN) immune subsets, in a syngeneic model, developed orthotopically with 4T1 cells in H4R knockout (H4R-KO) and wild-type mice.
RESULTS
Mice lacking H4R show reduced tumour size and weight, decreased number of lung metastases and percentage of CD4
CONCLUSIONS
This is the first report that demonstrates the participation of H4R in antitumour immunity, suggesting that H4R could be a target for cancer treatment.

Identifiants

pubmed: 29988113
doi: 10.1038/s41416-018-0173-z
pii: 10.1038/s41416-018-0173-z
pmc: PMC6325108
doi:

Substances chimiques

Antigens, CD19 0
Forkhead Transcription Factors 0
Foxp3 protein, mouse 0
Receptors, Histamine H4 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

128-138

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Auteurs

Helena A Sterle (HA)

Neuroimmunomodulation and Molecular Oncology Division, Institute for Biomedical Research (BIOMED), School of Medical Sciences, Pontifical Catholic University of Argentina (UCA), and the National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina.

Melisa B Nicoud (MB)

Laboratory of Tumor Biology and Inflammation, Institute for Biomedical Research (BIOMED), School of Medical Sciences, Pontifical Catholic University of Argentina (UCA), and the National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina.
Laboratory of Radioisotopes, School of Pharmacy and Biochemistry, University of Buenos Aires, Buenos Aires, Argentina.

Noelia A Massari (NA)

Immunology Department, School of Natural Sciences, National University of Patagonia San Juan Bosco, Chubut, Argentina.

Mónica A Táquez Delgado (MA)

Laboratory of Tumor Biology and Inflammation, Institute for Biomedical Research (BIOMED), School of Medical Sciences, Pontifical Catholic University of Argentina (UCA), and the National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina.

María V Herrero Ducloux (MV)

Pathology Department, School of Natural Sciences, National University of Patagonia San Juan Bosco, Chubut, Argentina.

Graciela A Cremaschi (GA)

Neuroimmunomodulation and Molecular Oncology Division, Institute for Biomedical Research (BIOMED), School of Medical Sciences, Pontifical Catholic University of Argentina (UCA), and the National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina.
Laboratory of Radioisotopes, School of Pharmacy and Biochemistry, University of Buenos Aires, Buenos Aires, Argentina.

Vanina A Medina (VA)

Laboratory of Tumor Biology and Inflammation, Institute for Biomedical Research (BIOMED), School of Medical Sciences, Pontifical Catholic University of Argentina (UCA), and the National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina. vmedina@ffyb.uba.ar.
Laboratory of Radioisotopes, School of Pharmacy and Biochemistry, University of Buenos Aires, Buenos Aires, Argentina. vmedina@ffyb.uba.ar.

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