The VEGF Pathway in Cancer and Disease: Responses, Resistance, and the Path Forward

被引:171
作者
Kieran, Mark W. [1 ,2 ]
Kalluri, Raghu [3 ]
Cho, Yoon-Jae [4 ,5 ]
机构
[1] Dana Farber Canc Inst, Dept Pediat Med Neurooncol, Boston, MA 02115 USA
[2] Childrens Hosp, Div Pediat Oncol, Boston, MA 02115 USA
[3] Beth Israel Deaconess Med Ctr, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[4] Stanford Univ, Dept Neurol & Neurosurg, Stanford, CA 94305 USA
[5] Lucile Packard Childrens Hosp, Stanford, CA 94305 USA
关键词
ENDOTHELIAL-GROWTH-FACTOR; PHASE-II TRIAL; TYROSINE KINASE INHIBITOR; RENAL-CELL CARCINOMA; ACUTE MYELOID-LEUKEMIA; BEVACIZUMAB PLUS IRINOTECAN; ANTIANGIOGENIC AGENT SU5416; RECEPTOR INHIBITOR; SMALL-MOLECULE; ANGIOGENESIS INHIBITOR;
D O I
10.1101/cshperspect.a006593
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Antiangiogenesis was proposed as a novel target for the treatment of cancer 40 years ago. Since the original hypothesis put forward by Judah Folkman in 1971, factors that mediate angiogenesis, their cellular targets, many of the pathways they signal, and inhibitors of the cytokines and receptors have been identified. Vascular endothelial growth factor (VEGF) is the most prominent among the angiogenic cytokines and is believed to play a central role in the process of neovascularization, both in cancer as well as other inflammatory diseases. This article reviews the biology of VEGF and its receptors, the use of anti-VEGF approaches in clinical disease, the toxicity of these therapies, and the resistance mechanisms that have limited the activity of these agents when used as monotherapy.
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页数:17
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