Williams Cecilia, Lin Chin-Yo
Center for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas 77204, USA.
Ecancermedicalscience. 2013 Nov 5;7:370. doi: 10.3332/ecancer.2013.370.
Since the discovery of the connection between ovarian hormones and breast cancer, endocrine therapy has been an integral adjuvant treatment for patients with hormone-dependent breast cancers. Oestrogen receptor (ER) plays a central role in mediating the effects of endogenous hormones and therapeutic agents. ER serves as a prognostic marker for responsiveness to endocrine therapy and is targeted either directly by selective oestrogen receptor modulators (SERMs) and pure antagonists or indirectly by aromatase inhibitors (AIs) that block oestrogen production. A significant number of ER-positive patients, however, fail to respond to therapy or develop resistance over time. This review focuses on the current understanding of ER functions and recent advances in genomic technologies and research that have provided a global perspective on hormone and ER activity and led to a number of significant discoveries, including the roles of co-regulatory factors and non-coding RNAs. Mechanistic insights into normal ER functions and therapeutic actions of SERMs and AIs will enable the development of better predictive markers and more effective target mechanisms and ultimately facilitate improvements in disease outcomes and patient survival.
自从发现卵巢激素与乳腺癌之间的联系以来,内分泌治疗一直是激素依赖性乳腺癌患者不可或缺的辅助治疗方法。雌激素受体(ER)在介导内源性激素和治疗药物的作用中起着核心作用。ER作为内分泌治疗反应性的预后标志物,可被选择性雌激素受体调节剂(SERM)和纯拮抗剂直接靶向,或被阻断雌激素生成的芳香化酶抑制剂(AI)间接靶向。然而,相当数量的ER阳性患者对治疗无反应或随着时间的推移产生耐药性。本综述重点关注对ER功能的当前理解以及基因组技术和研究的最新进展,这些进展提供了关于激素和ER活性的全局视角,并导致了许多重大发现,包括共调节因子和非编码RNA的作用。对正常ER功能以及SERM和AI治疗作用的机制性见解将有助于开发更好的预测标志物和更有效的靶向机制,并最终促进疾病结局和患者生存率的改善。