Chen James K
Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Nat Prod Rep. 2016 May 4;33(5):595-601. doi: 10.1039/c5np00153f.
Covering: 1950s to 2015During the 1950s, sheep ranchers in the western United States experienced episodic outbreaks of cyclopic lambs. In this highlight I describe how these mysterious incidents were traced to the grazing of Veratrum californicum wildflowers by pregnant ewes, leading to the discovery of cyclopamine () as a plant-derived teratogen. The precise mechanism of cyclopamine action remained enigmatic for 30 years, until this steroid alkaloid was found to be the first specific inhibitor of Hedgehog (Hh) signalling and a direct antagonist of the transmembrane receptor Smoothened (SMO). In addition to being a valuable probe of Hh pathway function, cyclopamine has been used to demonstrate the therapeutic potential of Hh pathway inhibitors. I discuss the development of SMO antagonists as anticancer therapies and emerging challenges.
20世纪50年代至2015年
在20世纪50年代,美国西部的牧羊业主经历了独眼羔羊的间歇性疫情爆发。在本综述中,我描述了这些神秘事件是如何追溯到怀孕母羊食用加州藜芦野花,从而导致发现环杷明()作为一种植物源性致畸剂的。环杷明作用的确切机制在30年里一直是个谜,直到这种甾体生物碱被发现是刺猬信号通路(Hh)的首个特异性抑制剂以及跨膜受体平滑受体(SMO)的直接拮抗剂。除了作为Hh信号通路功能的有价值探针外,环杷明还被用于证明Hh信号通路抑制剂的治疗潜力。我将讨论SMO拮抗剂作为抗癌疗法的发展以及新出现的挑战。