EPI-001, a compound active against castration-resistant prostate cancer, targets transactivation unit 5 of the androgen receptor

Castration-resistant prostate cancer is the lethal condition suffered by prostate cancer patients that become refractory to androgen deprivation therapy. EPI-001 is a recently identified compound active against this condition that modulates the activity of the androgen receptor, a nuclear receptor t...

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Detalhes bibliográficos
Autores: Mol, Eva de, Fenwick, R. Bryn, Phang, Christopher T. W., Buzón Redorta, Víctor, Szulc, Elzbieta Maria, Fuente Cebrián, Àlex de la, Escobedo Pascual, Albert, García Arroyo, Jesús, Bertoncini, Carlos W., Estébanez Perpiñá, Eva, McEwan, Iain J., Riera i Escalé, Antoni, Salvatella i Giralt, Xavier
Formato: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2016
País:España
Recursos:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/102449
Acesso em linha:https://hdl.handle.net/2445/102449
Access Level:acceso abierto
Palavra-chave:Càncer de pròstata
Receptors nuclears (Bioquímica)
Prostate cancer
Nuclear receptors (Biochemistry)
Descrição
Resumo:Castration-resistant prostate cancer is the lethal condition suffered by prostate cancer patients that become refractory to androgen deprivation therapy. EPI-001 is a recently identified compound active against this condition that modulates the activity of the androgen receptor, a nuclear receptor that is essential for disease progression. The mechanism by which this compound exerts its inhibitory activity is however not yet fully understood. Here we show, by using high resolution solution nuclear magnetic resonance spectroscopy, that EPI-001 selectively interacts with a partially folded region of the transactivation domain of the androgen receptor, known as transactivation unit 5, that is key for the ability of prostate cells to proliferate in the absence of androgens, a distinctive feature of castration-resistant prostate cancer. Our results can contribute to the development of more potent and less toxic novel androgen receptor antagonists for treating this disease.