类固醇
受体
类固醇激素
糖皮质激素受体
核受体
细胞生物学
配体(生物化学)
辅因子
类固醇激素受体
心理压抑
激素
化学
生物
生物化学
转录因子
基因
酶
遗传学
基因表达
癌症
雌激素受体
乳腺癌
作者
S. Stoney Simons,Raj Kumar
标识
DOI:10.1016/j.mce.2013.06.007
摘要
Steroid hormones, acting through their cognate receptor proteins, see widespread clinical applications due to their ability to alter the induction or repression of numerous genes. However, steroid usage is limited by the current inability to control off-target, or non-specific, side-effects. Recent results from three separate areas of research with glucocorticoid and other steroid receptors (cofactor-induced changes in receptor structure, the ability of ligands to alter remote regions of receptor structure, and how cofactor concentration affects both ligand potency and efficacy) indicate that a key element of receptor activity is the intrinsically disordered amino-terminal domain. These results are combined to construct a novel framework within which to logically pursue various approaches that could afford increased selectivity in steroid-based therapies.
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