维莫德吉
平滑
刺猬
刺猬信号通路
药理学
医学
基底细胞癌
癌症
癌症研究
生物信息学
生物
信号转导
内科学
生物化学
基底细胞
作者
Christian Espinosa‐Bustos,Jaime Mella,Jorge Soto‐Delgado,Cristian O. Salas
标识
DOI:10.4155/fmc-2018-0497
摘要
Since the Hedgehog signaling pathway has been associated with cancer, it has emerged as a therapeutic target for cancer therapy. The main target among the key Hedgehog proteins is the GPCR-like Smo receptor. Therefore, some Smo antagonists that have entered clinical trials, including the US FDA-approved drugs vismodegib and sonidegib, to treat basal cell carcinoma and medulloblastoma. However, early resistance of these drugs has spawned the need to understand the molecular bases of this phenomena. We therefore reviewed details about Smo receptor structures and the best Smo antagonist chemical structures. In addition, we discussed strategies that should be considered to develop new, safer generations of Smo antagonists that avoid current clinical limitations.
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