Selective VEGFR Inhibitors for Anticancer Therapeutics in Clinical Use and Clinical Trials

被引:24
|
作者
Zhang, Cunlong [1 ]
Tan, Chunyan [1 ,2 ]
Ding, Huaiwei [2 ]
Xin, Tian [1 ]
Jiang, Yuyang [1 ,3 ]
机构
[1] Tsinghua Univ, Grad Sch Shenzhen, State Key Lab Breeding Base Chem Biol, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Shenzhen Antitumor Drug Dev Engn Lab, Grad Sch Shenzhen, Shenzhen 518055, Peoples R China
[3] Tsinghua Univ, Sch Med, Dept Pharmacol & Pharmaceut Sci, Beijing 100084, Peoples R China
关键词
Selective; VEGFR inhibitor; anticancer; angiogenesis; ENDOTHELIAL-GROWTH-FACTOR; TYROSINE-KINASE-INHIBITOR; RENAL-CELL CARCINOMA; TRIPLE ANGIOKINASE INHIBITOR; PHASE-III TRIAL; ORAL MULTIKINASE INHIBITOR; REGORAFENIB BAY 73-4506; I DOSE-ESCALATION; SMALL-MOLECULE INHIBITORS; FACTOR RECEPTOR 2;
D O I
10.2174/138161212800672732
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Angiogenesis and vasculogenesis, regulated by VEGF/VEGFR signaling pathways, play key roles in tumor growth and metastasis. Selective inhibition of VEGFR kinase has been explored as a highly successful clinical strategy in cancer treatment. A number of VEGFR inhibitors have been approved in clinical use and many more are in various stages of drug development. This paper reviews selective small-molecule VEGFR inhibitors in clinical uses and in clinical trials, with particular focus on in vitro, in vivo and clinical trial results of these inhibitors. The VEGF/VEGFR genes and signaling pathways involved in tumor angiogenesis, and the strategies for accessing and improving the therapeutic efficacy of VEGFR inhibitors are also discussed.
引用
收藏
页码:2921 / 2935
页数:15
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