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Immunoprophylactic and immunotherapeutic control of hormone receptor-positive breast cancer
A. Buqué, N. Bloy, M. Perez-Lanzón, K. Iribarren, J. Humeau, JG. Pol, S. Levesque, L. Mondragon, T. Yamazaki, A. Sato, F. Aranda, S. Durand, A. Boissonnas, J. Fucikova, L. Senovilla, D. Enot, M. Hensler, M. Kremer, G. Stoll, Y. Hu, C. Massa, SC....
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem, Research Support, U.S. Gov't, Non-P.H.S.
NLK
Directory of Open Access Journals
od 2015
Free Medical Journals
od 2010
Nature Open Access
od 2010-12-01
PubMed Central
od 2012
Europe PubMed Central
od 2012
ProQuest Central
od 2010-01-01
Open Access Digital Library
od 2015-01-01
Open Access Digital Library
od 2015-01-01
Medline Complete (EBSCOhost)
od 2012-11-01
Health & Medicine (ProQuest)
od 2010-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2010
Springer Nature OA/Free Journals
od 2010-12-01
- MeSH
- 9,10-dimethyl-1,2-benzanthracen MeSH
- analýza přežití MeSH
- experimentální nádory mléčných žláz chemicky indukované imunologie prevence a kontrola MeSH
- imunoterapie metody MeSH
- interferon typ I imunologie metabolismus MeSH
- karcinogeneze účinky léků imunologie MeSH
- lidé MeSH
- medroxyprogesteronacetát MeSH
- myši inbrední BALB C MeSH
- myši inbrední C57BL MeSH
- myši knockoutované MeSH
- nádory prsu imunologie metabolismus terapie MeSH
- niacinamid aplikace a dávkování MeSH
- progrese nemoci MeSH
- receptor erbB-2 imunologie metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
Hormone receptor (HR)+ breast cancer (BC) causes most BC-related deaths, calling for improved therapeutic approaches. Despite expectations, immune checkpoint blockers (ICBs) are poorly active in patients with HR+ BC, in part reflecting the lack of preclinical models that recapitulate disease progression in immunocompetent hosts. We demonstrate that mammary tumors driven by medroxyprogesterone acetate (M) and 7,12-dimethylbenz[a]anthracene (D) recapitulate several key features of human luminal B HR+HER2- BC, including limited immune infiltration and poor sensitivity to ICBs. M/D-driven oncogenesis is accelerated by immune defects, demonstrating that M/D-driven tumors are under immunosurveillance. Safe nutritional measures including nicotinamide (NAM) supplementation efficiently delay M/D-driven oncogenesis by reactivating immunosurveillance. NAM also mediates immunotherapeutic effects against established M/D-driven and transplantable BC, largely reflecting increased type I interferon secretion by malignant cells and direct stimulation of immune effector cells. Our findings identify NAM as a potential strategy for the prevention and treatment of HR+ BC.
Caryl and Israel Englander Institute for Precision Medicine New York NY USA
Department of Cancer Medicine Gustave Roussy Cancer Center Villejuif France
Department of Radiation Oncology Weill Cornell Medical College New York NY USA
Gustave Roussy Cancer Center Villejuif France
Institute of Medical Immunology Martin Luther University Halle Wittenberg Halle Germany
Sorbonne Université Inserm CNRS Centre d'Immunologie et des Maladies Infectieuses CIMI Paris France
Citace poskytuje Crossref.org
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- $a Buqué, Aitziber $u Department of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA. Equipe labellisée par la Ligue contre le cancer, Centre de Recherche des Cordeliers, INSERM U1138, Université de Paris, Sorbonne Université, Paris, France.
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- $a Hormone receptor (HR)+ breast cancer (BC) causes most BC-related deaths, calling for improved therapeutic approaches. Despite expectations, immune checkpoint blockers (ICBs) are poorly active in patients with HR+ BC, in part reflecting the lack of preclinical models that recapitulate disease progression in immunocompetent hosts. We demonstrate that mammary tumors driven by medroxyprogesterone acetate (M) and 7,12-dimethylbenz[a]anthracene (D) recapitulate several key features of human luminal B HR+HER2- BC, including limited immune infiltration and poor sensitivity to ICBs. M/D-driven oncogenesis is accelerated by immune defects, demonstrating that M/D-driven tumors are under immunosurveillance. Safe nutritional measures including nicotinamide (NAM) supplementation efficiently delay M/D-driven oncogenesis by reactivating immunosurveillance. NAM also mediates immunotherapeutic effects against established M/D-driven and transplantable BC, largely reflecting increased type I interferon secretion by malignant cells and direct stimulation of immune effector cells. Our findings identify NAM as a potential strategy for the prevention and treatment of HR+ BC.
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