Molecular mechanism of a cross-talk between estrogen and growth-factor signaling pathways

被引:37
作者
Kato, S [1 ]
Kitamoto, T [1 ]
Masuhiro, Y [1 ]
Yanagisawa, J [1 ]
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
关键词
estrogen receptor; transcription; mitogen-activated protein kinase; co-activator; transactivation domain;
D O I
10.1159/000055253
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The actions of estrogen (E-2) are considered to be mediated through its nuclear E-2 receptor (ER). In cancer development, growth factors are shown to act synergistically with E-2. Recently we found that the mitogen-activated protein kinase, activated by growth factors, phosphorylates human ER alpha and this phosphorylation potentiates the transactivation function of human ER alpha demonstrating a novel cross-talk between E-2 and growth factor-signaling pathways. In this review, the molecular mechanism of this cross-talk is discussed.
引用
收藏
页码:5 / 10
页数:6
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