Targeting von Hippel-Lindau pathway in renal cell carcinoma

被引:145
|
作者
Patel, Premal H.
Chadalavada, Rajendrakumar S. V.
Chaganti, R. S. K.
Motzer, Robert J.
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Cell Biol Program, New York, NY 10021 USA
关键词
D O I
10.1158/1078-0432.CCR-06-2254
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Inheritance of a defective copy of the von Hippel-Lindau (VHL) gene leads to the most common cause of inherited renal cell carcinoma (RCC). In addition, most patients with sporadic RCC have aberrant VHL. In the absence of VHL, hypoxia-inducible factor alpha accumulates, leading to production of several growth factors, including vascular endothelial growth factor and platelet-derived growth factor. We review here the biology of RCC and how a combination of proximal and distal block of VHL/hypoxia-inducible factor alpha pathway by novel targeted agents, including sunitinib, sorafenib, bevacizumab, everolimus, and temsirolimus, has led to significant improvements in progression-free survival.
引用
收藏
页码:7215 / 7220
页数:6
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