Salvino Joseph M, Srikanth Yellamelli V V, Lou Rongliang, Oyer Halley M, Chen Nan, Kim Felix J
Department of Pharmacology and Physiology, Drexel University College of Medicine, 245 N 15th Street, Philadelphia, PA 19102-1101, USA.
Department of Pharmacology and Physiology, Drexel University College of Medicine, 245 N 15th Street, Philadelphia, PA 19102-1101, USA.
Bioorg Med Chem Lett. 2017 May 15;27(10):2216-2220. doi: 10.1016/j.bmcl.2017.03.030. Epub 2017 Mar 18.
Prostate cancer is the most frequently diagnosed malignancy and the leading cause of cancer related death in men. First line therapy for disseminated disease relies on androgen deprivation, leveraging the addiction of these tumors on androgens for both growth and survival. Treatment typically involves antagonizing the androgen receptor (AR) or blocking the synthesis of androgens. Recurrence is common and within 2-3years patients develop castration resistant tumors that become unresponsive to AR-axis targeted therapies. In order to provide a more effective treatment, we are utilizing an approach that targets a key scaffolding protein, Sigma1 (also known as sigma-1 receptor), a unique 26-kilodalton integral membrane protein that is critical in stabilizing the AR. Herein we report on a new series of Sigma1 compounds for lead optimization derived from a hybrid pharmacophore approach.
前列腺癌是男性中最常被诊断出的恶性肿瘤,也是癌症相关死亡的主要原因。针对播散性疾病的一线治疗依赖于雄激素剥夺,利用这些肿瘤对雄激素在生长和存活方面的依赖性。治疗通常包括拮抗雄激素受体(AR)或阻断雄激素的合成。复发很常见,在2至3年内患者会发展出对去势抵抗的肿瘤,这些肿瘤对AR轴靶向治疗不再有反应。为了提供更有效的治疗方法,我们正在采用一种靶向关键支架蛋白Sigma1(也称为sigma-1受体)的方法,Sigma1是一种独特的26千道尔顿整合膜蛋白,对稳定AR至关重要。在此,我们报告了一系列基于杂交药效团方法衍生的用于先导优化的新型Sigma1化合物。