17β-Estradiol transcriptionally represses human insulin receptor gene expression causing cellular insulin resistance

被引:20
作者
García-Arencibia, M
Molero, S
Dávila, N
Carranza, MC
Calle, C [1 ]
机构
[1] Univ Complutense, Sch Med, Dept Biochem & Mol Biol, E-28040 Madrid, Spain
[2] Puerto Hierro Hosp, Biochem Unit, Madrid 28040, Spain
关键词
17; beta-Estradiol; human insulin receptor gene; transcriptional repression; insulin resistance; cell survival; DNA synthesis; glucose transport; glucose oxidation; U-937; cells;
D O I
10.1016/j.leukres.2004.05.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this study, we demonstrate that 17beta-estradiol (E-2) inhibits human insulin receptor (IR) gene expression in a dose- and time-dependent manner in U-937 human promonocytic cells. Using cells transfected with the -1819 to -271 bp fragment of the human IR promoter (wild type promoter) and treated with E-2, we show that this repression is regulated at the transcriptional level. The steroid was also found to diminish the insulin responsiveness of the cells in terms of cell survival, DNA synthesis, glucose transport, and glucose oxidation, this last effect possibly involving reduced phosphatidylinositol 3-kinase (PI3-kinase) activity. These data provide new information on the molecular mechanisms of estrogen-inducing insulin resistance in human cells. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:79 / 87
页数:9
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