Antiangiogenic Therapy for Cancer: An Update

被引:171
作者
Al-Husein, Belal
Abdalla, Maha
Trepte, Morgan
DeRemer, David L.
Somanath, Payaningal R. [1 ,2 ]
机构
[1] Georgia Hlth Sci Univ, Univ Georgia, Coll Pharm, Dept Med, Augusta, GA 30912 USA
[2] Charlie Norwood VA Med Ctr, Augusta, GA USA
来源
PHARMACOTHERAPY | 2012年 / 32卷 / 12期
基金
美国国家卫生研究院;
关键词
tumor angiogenesis; bevacizumab; antiangiogenic therapy; cancer; RENAL-CELL CARCINOMA; ENDOTHELIAL GROWTH-FACTOR; PHASE-III TRIAL; PACLITAXEL PLUS BEVACIZUMAB; DOUBLE-BLIND; 1ST-LINE THERAPY; BREAST-CANCER; 2ND-LINE TREATMENT; INDUCED APOPTOSIS; INTERFERON-ALPHA;
D O I
10.1002/phar.1147
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The idea of antiangiogenic therapy was the brainchild of Dr. Judah Folkman in the early 1970s. He proposed that by cutting off the blood supply, cancer cells would be deprived of nutrients and, hence, treated. His efforts paid off when bevacizumab, a monoclonal antibody targeting vascular endothelial growth factor, was approved as antiangiogenic therapy in 2004 for the treatment of colon cancer. Since then, an array of antiangiogenic inhibitors, either as monotherapy or in combination with other cytotoxic and chemotherapy drugs, have been developed, used in clinical trials, and approved for the treatment of cancer. Despite this important breakthrough, antiangiogenic therapy for cancer met with a number of hurdles on its way to becoming an option for cancer therapy. In this article, we summarize the most current information on the mechanisms of tumor angiogenesis, proangiogenic and antiangiogenic factors, potential targets and their mechanisms of action, and experimental evidences, as well as the most recent clinical trial data on antiangiogenic agents for cancer therapy.
引用
收藏
页码:1095 / 1111
页数:17
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