De Mol Eva, Fenwick R Bryn, Phang Christopher T W, Buzón Victor, Szulc Elzbieta, de la Fuente Alex, Escobedo Albert, García Jesús, Bertoncini Carlos W, Estébanez-Perpiñá Eva, McEwan Iain J, Riera Antoni, Salvatella Xavier
Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology , Baldiri Reixac 10, 08028 Barcelona, Spain.
Departament de Bioquímica i Biología Molecular, and Institute of Biomedicine, University of Barcelona (IBUB) , Baldiri Reixac 10, 08028 Barcelona, Spain.
ACS Chem Biol. 2016 Sep 16;11(9):2499-505. doi: 10.1021/acschembio.6b00182. Epub 2016 Jul 14.
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.
去势抵抗性前列腺癌是前列腺癌患者所患的致命病症,这些患者对雄激素剥夺疗法产生了耐药性。EPI-001是最近发现的一种对这种病症有效的化合物,它可调节雄激素受体的活性,雄激素受体是一种对疾病进展至关重要的核受体。然而,这种化合物发挥其抑制活性的机制尚未完全明确。在此,我们通过使用高分辨率溶液核磁共振光谱表明,EPI-001选择性地与雄激素受体反式激活结构域的一个部分折叠区域相互作用,该区域称为反式激活单元5,它是前列腺细胞在无雄激素情况下增殖能力的关键,而这是去势抵抗性前列腺癌的一个显著特征。我们的研究结果有助于开发更有效且毒性更低的新型雄激素受体拮抗剂来治疗这种疾病。