MODULATION OF ESTROGEN-RECEPTOR ACTIVITY BY ESTROGENS AND ANTIESTROGENS

被引:47
作者
GREEN, S
机构
[1] Imperial Chemical Industries, Cental Toxicology Laboratory, Macclesfield, Cheshire SK10 4TJ England, Alderly Park
关键词
D O I
10.1016/0960-0760(90)90415-H
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The oestrogen receptor is a member of a supergene family that includes receptors for steroid and thyroid hormones, vitamin D3, and retinoic acid. A number of additional members of the family have been cloned where the putative ligand remains to be identified. The oestrogen receptor is a ligand-activated transcription factor that modulates specific gene expression by binding to short DNA sequences (oestrogen response elements) located in the vicinity of oestrogen-regulated genes. Regions of the receptor responsible for hormone-binding, DNA-binding and activation of transcription, have been identified. The anti-oestrogen, tamoxifen (Nolvadex), behaves as a weak oestrogen agonist. A model, based upon our current understanding of the molecular mechanism of oestrogen action, will be presented to explain the cell and gene specific effects of some anti-oestrogens.
引用
收藏
页码:747 / 751
页数:5
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