ACTION OF PURE ANTIESTROGENS IN INHIBITING ESTROGEN-RECEPTOR ACTION

被引:119
作者
PARKER, MG
机构
[1] Imperial Cancer Research Fund, Lincoln's Inn Fields, Laboratory Of Molecular Endocrinology, London
关键词
ESTROGEN RECEPTOR; ANTIESTROGENS; DNA BINDING; PROTEIN TURNOVER;
D O I
10.1007/BF00689686
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The mechanism of action of the pure antiestrogens ICI 164384 and ICI 182780 has been investigated. Both antagonists are steroidal antiestrogens with 7alpha-alkylamide side-chains. The antiestrogens reduce the cellular content of the estrogen receptor by reducing the half-life of the protein. A potential mechanism for this effect is suggested by the observation that the DNA binding activity of receptors which have been over-expressed in cells was inhibited in vitro. The inhibitory activity of analogues of ICI 164384 with different side chain lengths correlates with their ability to function as pure antiestrogens in vivo. Since the estrogen binding site overlaps with residues involved in dimerisation, the antiestrogens are likely to bind to a similar site and may therefore interfere with receptor dimerisation in the hormone binding domain by means of the 7alpha side-chain. We propose that the increased turnover of the receptor in the presence of ICI 164384 and ICI 182380 is a consequence of impaired dimerisation of the proteins.
引用
收藏
页码:131 / 137
页数:7
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