Biomedical Engineering, Vanderbilt University, Nashville, TN, USA.
Pathology, Microbiology & Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
FEBS J. 2023 Apr;290(8):1943-1953. doi: 10.1111/febs.16407. Epub 2022 Feb 28.
The molecular mechanisms regulating oestrogen homeostasis have been primarily studied in the mammary gland, which is the focus of this review. In the non-pregnant adult, the mammary gland undergoes repeated cycles of proliferation and apoptosis in response to the fluctuating levels of oestrogen that occur during the reproductive stage. Oestrogen actions are mediated through the steroid hormone receptors, oestrogen receptor α and β and through a G-protein coupled receptor. In the mammary gland, ERα is of particular importance and thus will be highlighted. Mechanisms regulating oestrogen-induced responses through ERα are necessary to maintain homeostasis given that the signalling pathways that are activated in response to ERα-mediated transcription can also induce transformation. ERK1/2 and its downstream effector, p90 ribosomal S6 kinase (RSK), control homeostasis in the mammary gland by limiting oestrogen-mediated ERα responsiveness. ERK1/2 drives degradation coupled ERα-mediated transcription, whereas RSK2 acts as a negative regulator of ERK1/2 activity to limit oestrogen responsiveness. Moreover, RSK2 acts as a positive regulator of translation. Thus, RSK2 provides both positive and negative signals to maintain oestrogen responsiveness. In addition to transmitting signals through tyrosine kinase receptors, ERK1/2-RSK engages with hedgehog signalling to maintain oestrogen levels and with the HIPPO pathway to regulate ERα-mediated transcription. Additionally, ERK1/2-RSK controls the progenitor populations within the mammary gland to maintain the ERα-positive population. RSK2 is involved in increased breast cancer risk in individuals taking oral contraceptives and in parity-induced protection against breast cancer. RSK2 and ERα may also co-operate in diseases in tissues outside of the mammary gland.
调节雌激素稳态的分子机制主要在乳腺中进行了研究,这是本综述的重点。在非妊娠的成年期,乳腺会对生殖阶段雌激素水平的波动做出反复的增殖和凋亡反应。雌激素作用是通过甾体激素受体,即雌激素受体α和β,以及 G 蛋白偶联受体来介导的。在乳腺中,ERα 尤为重要,因此将重点介绍。调节 ERα 介导的雌激素反应的机制对于维持稳态是必要的,因为激活的信号通路不仅可以诱导转录,还可以诱导转化。ERK1/2 及其下游效应物 p90 核糖体 S6 激酶(RSK)通过限制雌激素介导的 ERα 反应性来控制乳腺中的稳态。ERK1/2 驱动与 ERα 介导的转录偶联的降解,而 RSK2 作为 ERK1/2 活性的负调节剂,限制雌激素反应性。此外,RSK2 作为翻译的正调节剂。因此,RSK2 为维持雌激素反应性提供了正负信号。除了通过酪氨酸激酶受体传递信号外,ERK1/2-RSK 还与 Hedgehog 信号通路相互作用,以维持雌激素水平,并与 HIPPO 通路相互作用,调节 ERα 介导的转录。此外,ERK1/2-RSK 控制乳腺中的祖细胞群体,以维持 ERα 阳性细胞群体。RSK2 参与了口服避孕药使用者乳腺癌风险的增加以及生育诱导对乳腺癌的保护。RSK2 和 ERα 也可能在乳腺外组织的疾病中协同作用。