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Aromatase, its inhibitors and their use in breast cancer treatment.

作者信息

Brodie A M

机构信息

Department of Pharmacology, School of Medicine, University of Maryland, Baltimore 21201-1559.

出版信息

Pharmacol Ther. 1993 Dec;60(3):501-15. doi: 10.1016/0163-7258(93)90033-a.

DOI:10.1016/0163-7258(93)90033-a
PMID:8073072
Abstract

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.

摘要

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