Hedgehog pathway inhibition and the race against tumor evolution

被引:88
作者
Atwood, Scott X. [1 ]
Chang, Anne Lynn S. [1 ]
Oro, Anthony E. [1 ]
机构
[1] Stanford Univ, Sch Med, Program Epithelial Biol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
BASAL-CELL CARCINOMA; INTRAFLAGELLAR TRANSPORT; ACQUIRED-RESISTANCE; GLI PROTEINS; TRANSCRIPTION; MECHANISMS; CANCERS; DISEASE;
D O I
10.1083/jcb.201207140
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dependence of basal cell carcinomas and medulloblastomas on the Hedgehog pathway provides an opportunity for targeted or "personalized" therapy. The recent effectiveness and FDA approval of the first Smoothened inhibitors validates this class of agents, but has revealed drug-resistant tumor variants that bypass Smoothened inhibition. Here, we summarize the effectiveness of Hedgehog pathway inhibitors and highlight promising areas for the development of next generation drug antagonists for Hedgehog-dependent cancers.
引用
收藏
页码:193 / 197
页数:5
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