雌激素受体
化学
兴奋剂
受体
转录因子
雌激素受体
细胞生物学
核受体
生物
分子生物学
生物化学
基因
遗传学
癌症
乳腺癌
作者
Zhaohu Lin,Hong Shen,Jin Huang,Shuai Chen,Lili Chen,Jing Chen,Guixia Liu,Hualiang Jiang,Xu Shen
标识
DOI:10.1016/j.jsbmb.2008.03.028
摘要
Estrogen receptors (ERs) belong to nuclear hormone receptor superfamily and can be activated by estrogens and regulate many target genes. Two ER isoforms, ERα and ERβ have been discovered to date and ERβ was indicated to involve in anti-inflammatory and anti-diabetogenic effects. Recently, some studies also demonstrated an association between ERβ and GLUT4 expression. The development of selective ERβ ligand has facilitated probing its novel biological functions and clinical benefits. In this work, a new ERβ selective agonist, butyl 4-(butyryloxy)benzoate (DCW234), was discovered as investigated by surface plasmon resonance (SPR) technology, yeast two-hybrid and cell-based transcription-based assays. SPR results demonstrated that DCW234 has a higher binding affinity against ERβ over ERα and induces a strong and selective stimulation on ERβ/SRC1 interaction, which could be efficiently blocked by Tamoxifen. Meanwhile, the yeast two-hybrid technology-based assay indicated that DCW234 exhibits a higher agonistic activity (∼13-fold) in stimulating ERβ ligand-binding domain (LBD) interaction with SRC1 (EC50 = 2.5 μM) than ERα-LBD/SRC1 interaction (EC50 = 32.7 μM). The cell-based transcriptional assay further proved the potency and selectivity of DCW234. Moreover, DCW234 was found to be able to induce GLUT4 expression in CHO-K1 cell. The discovered DCW234 might be hopefully developed as a potential lead compound for further research.
科研通智能强力驱动
Strongly Powered by AbleSci AI