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Mol Cancer Ther ; 20(5): 763-774, 2021 05.
Artículo en Inglés | MEDLINE | ID: mdl-33649102

RESUMEN

Numerous mechanisms of resistance arise in response to treatment with second-generation androgen receptor (AR) pathway inhibitors in metastatic castration-resistant prostate cancer (mCRPC). Among these, point mutations in the ligand binding domain can transform antagonists into agonists, driving the disease through activation of AR signaling. To address this unmet need, we report the discovery of JNJ-63576253, a next-generation AR pathway inhibitor that potently abrogates AR signaling in models of human prostate adenocarcinoma. JNJ-63576253 is advancing as a clinical candidate with potential effectiveness in the subset of patients who do not respond to or are progressing while on second-generation AR-targeted therapeutics.


Asunto(s)
Antagonistas de Receptores Androgénicos/uso terapéutico , Neoplasias de la Próstata Resistentes a la Castración/tratamiento farmacológico , Dominios Proteicos/genética , Antagonistas de Receptores Androgénicos/farmacología , Animales , Línea Celular Tumoral , Humanos , Ligandos , Masculino , Ratones , Modelos Moleculares , Mutación , Ratas , Ensayos Antitumor por Modelo de Xenoinjerto
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