AROMATASE, ITS INHIBITORS AND THEIR USE IN BREAST-CANCER-TREATMENT

被引:40
作者
BRODIE, AMH
机构
[1] Department of Pharmacology, School of Medicine, University of Maryland, Baltimore
关键词
AROMATASE INHIBITORS; BREAST CANCER TREATMENT; ESTROGEN;
D O I
10.1016/0163-7258(93)90033-A
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aromatase, a cytochrome P450 enzyme, catalyses the rate-limiting step in the biosynthesis of estrogens. Many processes in male and female development and reproduction and especially in the growth of hormone-dependent cancers, are dependent on estrogens. Therefore, controlling estrogen production by inhibition of aromatase is a logical treatment strategy. Two classes of aromatase inhibitors, steroidal and non-steroidal compounds, are now coming into use. Among the steroid substrate analogs, 4-hydroxyandrostenedione has been shown to be effective in breast cancer patients with advanced disease and was recently approved for treatment in the United Kingdom. Several highly potent and selective non-steroidal inhibitors are now in Clinical trials. The variety of compounds that act as aromatase inhibitors should provide breast cancer patients with a number of new treatment options.
引用
收藏
页码:501 / 515
页数:15
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