Center for BioSciences, Department of BioSciences and Nutrition, Karolinska Institutet, Stockholm, Sweden.
Biochem Biophys Res Commun. 2010 May 21;396(1):63-6. doi: 10.1016/j.bbrc.2010.02.144.
The discovery of ERbeta in the middle of the 1990s represents a paradigm shift in our understanding of estrogen signaling. It has turned out that estrogen action is not mediated by one receptor, ERalpha, but by two balancing factors, ERalpha and ERbeta, which are often antagonistic to one another. Excitingly, ERbeta has been shown to be widespread in the body and to be involved in a multitude of physiological and pathophysiological events. This has led to a strong interest of the pharmaceutical industry to target ERbeta by drugs against various diseases. In this review, focus is on the role of ERbeta in malignant diseases where the anti proliferative activity of ERbeta gives hope of new therapeutic approaches.
二十世纪九十年代中期 ERbeta 的发现代表了我们对雌激素信号转导理解的范式转变。事实证明,雌激素作用不是由一个受体 ERalpha 介导的,而是由两个平衡因子 ERalpha 和 ERbeta 介导的,它们通常相互拮抗。令人兴奋的是,已经表明 ERbeta 在体内广泛存在,并参与多种生理和病理生理事件。这导致了制药行业对通过针对各种疾病的药物靶向 ERbeta 产生了浓厚的兴趣。在这篇综述中,重点关注 ERbeta 在恶性疾病中的作用,其中 ERbeta 的抗增殖活性为新的治疗方法带来了希望。