Therapeutic targeting of HER2-CB2R heteromers in HER2-positive breast cancer

There is a subtype of breast cancer characterized by the overexpression of the oncogene HER2. Although most patients with this diagnosis benefit from HER2-targeted treatments, some do not respond to these therapies and others develop resistance with time. New tools are therefore warranted for the tr...

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Detalles Bibliográficos
Autores: Blasco-Benito, Sandra, Moreno Guillén, Estefanía, Seijo-Vila, Marta, Tundidor, Isabel, Andradas, Clara, Caffarel, María M., Caro-Villalobos, Miriam, Urigüen, Leyre, Diez-Alarcia, Rebeca, Moreno-Bueno, Gema, Hernández, Lucía, Manso, Luis, Homar Ruano, Patricia C., McCormick, Peter J., Bibic, Lucka, Bernadó Morales, Cristina, Arribas, Joaquín V. (Vicente), Canals Buj, Meritxell, Casadó, Vicent, Canela Campos, Enric I. (Enric Isidre), 1949-, Guzmán, Manuel, Pérez-Gómez, Eduardo, Sánchez Mora, Cristina
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2019
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/149576
Acceso en línea:https://hdl.handle.net/2445/149576
Access Level:acceso abierto
Palabra clave:Càncer de mama
Breast cancer
Descripción
Sumario:There is a subtype of breast cancer characterized by the overexpression of the oncogene HER2. Although most patients with this diagnosis benefit from HER2-targeted treatments, some do not respond to these therapies and others develop resistance with time. New tools are therefore warranted for the treatment of this patient population, and for early identification of those individuals at a higher risk of developing innate or acquired resistance to current treatments. Here, we show that HER2 forms heteromer complexes with the cannabinoid receptor CB2R, the expression of these structures correlates with poor patient prognosis, and their disruption promotes antitumor responses. Collectively, our results support HER2-CB2R heteromers as new therapeutic targets and prognostic tools in HER2+ breast cancer