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首页> 外文期刊>The Journal of Steroid Biochemistry and Molecular Biology >Hypoxic activation of unoccupied estrogen-receptor-alpha is mediated by hypoxia-inducible factor-1 alpha.
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Hypoxic activation of unoccupied estrogen-receptor-alpha is mediated by hypoxia-inducible factor-1 alpha.

机译:缺氧的雌激素受体α的低氧激活是由缺氧诱导因子1α介导的。

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摘要

The estrogen receptor (ER) plays an important role in breast cancer development and progression. Hypoxia has been shown to modulate the level of ERalpha expression, which is intimately associated with the biology of breast carcinomas. However, the effect of hypoxia on ERalpha-mediated transactivation is largely unknown. In this report, we have examined ligand-independent transcriptional activation of ERalpha by hypoxia. The hypoxia-induced ERalpha-mediated transcriptional response was inhibited by the ER antagonist ICI 182,780 as determined by transient expression of ERalpha and ER-responsive reporter plasmids in the HEK 293 cells. Hypoxic activation of ERalpha was dependent on the increased expression of hypoxia-inducible factor-1alpha (HIF-1alpha), as examined in HEK 293 cells under conditions of normoxia. These results indicate that hypoxia activates ERalpha in a ligand-independent manner, possibly through the interaction between HIF-1alpha and ERalpha.
机译:雌激素受体(ER)在乳腺癌的发生和发展中起着重要作用。缺氧已被证明可调节ERalpha的表达水平,而ERalpha的表达与乳腺癌的生物学密切相关。但是,缺氧对ERalpha介导的反式激活的影响很大程度上未知。在此报告中,我们检查了缺氧引起的ERalpha配体非依赖性转录激活。缺氧诱导的ERalpha介导的转录反应被ER拮抗剂ICI 182,780抑制,这由ERalpha和ER反应性报告质粒在HEK 293细胞中的瞬时表达确定。 ERalpha的缺氧激活取决于缺氧诱导因子-1alpha(HIF-1alpha)的表达增加,这是在常氧条件下在HEK 293细胞中检测到的。这些结果表明,缺氧可能以不依赖配体的方式激活ERalpha,可能是通过HIF-1alpha和ERalpha之间的相互作用。

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