交易激励
前列腺癌
雄激素受体
雄激素受体拮抗剂
癌症研究
雄激素剥夺疗法
内科学
雄激素
内分泌学
核受体
化学
生物
癌症
医学
激素
生物化学
转录因子
基因
作者
Eva De Mol,R. Bryn Fenwick,Christopher T. W. Phang,Víctor Buzón,Elzbieta Szulc,Alex de la Fuente,Albert Escobedo,Jesús García,Carlos W. Bertoncini,Eva Estébanez‐Perpiñá,Iain J. McEwan,Antoni Riéra,Xavier Salvatella
标识
DOI:10.1021/acschembio.6b00182
摘要
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.
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