University of California San Francisco, Department of Biochemistry and Biophysics, San Francisco, CA941432240, USA +1 415 476 5051 ; +1 415 476 1902 ;
Expert Opin Drug Discov. 2007 Oct;2(10):1341-55. doi: 10.1517/17460441.2.10.1341.
The androgen receptor (AR) regulates gene transcription in many tissues and is profoundly important in prostate cancer. Antiandrogens compete with the natural hormone and are front line therapeutics to treat prostate cancer. However, antiandrogens frequently become ineffective after prolonged treatment because of development of tumor resistance. This paper reviews design principles for new generations of antiandrogens: super antagonists and surface allosteric modulators. Super antiandrogens are compounds with higher binding affinity than natural agonists and that contain precisely engineered hydrophobic groups that disrupt AR function. AR surface is also an attractive alternative target. Surface inhibitors are small molecules that directly block the receptor-co-activator interface, preventing co-activator recruitment. The challenges to designing these compounds are significant but so is the potential for treatment of the disease.
雄激素受体(AR)在许多组织中调节基因转录,在前列腺癌中具有重要作用。抗雄激素与天然激素竞争,是治疗前列腺癌的一线治疗药物。然而,由于肿瘤耐药性的发展,抗雄激素在长期治疗后经常变得无效。本文综述了新一代抗雄激素的设计原则:超级拮抗剂和表面变构调节剂。超级抗雄激素是指比天然激动剂具有更高结合亲和力的化合物,并且包含经过精确设计的疏水性基团,这些基团破坏 AR 功能。AR 表面也是一个有吸引力的替代靶标。表面抑制剂是直接阻断受体-共激活剂界面的小分子,阻止共激活剂募集。设计这些化合物具有挑战性,但治疗疾病的潜力也很大。