Allosteric inhibition of HIF-2 as a novel therapy for clear cell renal cell carcinoma

被引:42
|
作者
Yu, Yancheng [1 ,2 ]
Yu, Quanwei [1 ,2 ]
Zhang, Xiaojin [1 ,2 ]
机构
[1] China Pharmaceut Univ, Jiangsu Key Lab Drug Design & Optimizat, Nanjing 211198, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Dept Chem, Nanjing 211198, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
HYPOXIA-INDUCIBLE FACTOR-2-ALPHA; PAS-B DOMAIN; TRANSCRIPTIONAL ACTIVATION; LIGAND-BINDING; HIF2-ALPHA; HIF-2-ALPHA; GROWTH; ANTAGONIST; TARGET; IDENTIFICATION;
D O I
10.1016/j.drudis.2019.09.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Clear cell renal cell carcinoma (ccRCC) is the most common subtype of RCC and bears a significantly high frequency of hypoxia-inducible factor 2 alpha (HIF-2 alpha) because of von Hippel-Lindau (VHL) tumor suppressor gene mutations. From the first discovery of HIF-2 alpha inhibitors to the promising potency of the HIF-2 alpha inhibitor PT2977 in a clinical Phase II trial for the treatment of advanced RCC, inhibition of HIF-2 alpha has proved to be a novel and effective therapy for RCC. In this review, we briefly discuss the role of HIF-2 alpha in ccRCC and provide insight into recent advances in the discovery, development, and mode of action of HIF-2 alpha allosteric inhibitors.
引用
收藏
页码:2332 / 2340
页数:9
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