Immunomodulatory role of histamine H4 receptor in breast cancer.
Animals
Antigens, CD19
/ immunology
Breast Neoplasms
/ genetics
CD4-Positive T-Lymphocytes
/ immunology
Female
Forkhead Transcription Factors
/ immunology
Humans
Immunomodulation
/ genetics
Killer Cells, Natural
/ immunology
Mice
Mice, Knockout
Receptors, Histamine H4
/ genetics
T-Lymphocytes, Regulatory
/ immunology
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
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
128-138Références
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