Role of the hypoxic tumor microenvironment in the resistance to anti-angiogenic therapies

被引:113
作者
Rapisarda, Annamaria [1 ]
Melillo, Giovanni [1 ]
机构
[1] NCI, Tumor Hypoxia Lab, SAIC Frederick Inc, Frederick, MD 21702 USA
基金
美国国家卫生研究院;
关键词
Angiogenesis; VEGF; Hypoxia; HIF-1; Bevacizumab; Cancer therapeutics; Topotecan; mTOR inhibitors; ENDOTHELIAL GROWTH-FACTOR; INDUCIBLE FACTOR-1-ALPHA PROTEIN; SMALL-MOLECULE INHIBITORS; CHEMOKINE RECEPTOR CXCR4; ANTIANGIOGENIC THERAPY; FACTOR-I; TRANSCRIPTIONAL ACTIVATION; DEPENDENT INHIBITION; PANCREATIC-CANCER; MALIGNANT GLIOMAS;
D O I
10.1016/j.drup.2009.03.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Angiogenesis, a key process for the growth of human cancers, has recently been exploited for the development of a novel class of cancer therapeutics that was thought to have wide applications and not to induce resistance in the clinical setting. Indeed, anti-angiogenic therapy has become an important option for the management of several human malignancies. However, a significant number of patients either do not respond to anti-angiogenic agents or fairly rapidly develop resistance. In addition, the benefit of anti-angiogenic therapy is relatively short-lived and the majority of patients eventually relapses and progresses. Several mechanisms of resistance to anti-angiogenic therapy have been recently proposed. The current review focuses on the role of intra-tumor hypoxia as a mechanism of resistance to anti-angiogenic agents and speculates on therapeutic approaches that might circumvent resistance and thereby improve clinical outcome. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:74 / 80
页数:7
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