Caringella A M, Di Naro E, Loverro G
Dipartimento di Ginecologia, Ostetricia e Neonatologia Università degli Studi di Bari, Bari, Italia.
Minerva Ginecol. 2011 Dec;63(6):495-504.
Approximately 70-80% of endometrial carcinomas, type I carcinomas, are associated with endometrial hyperplasia, hyperestrogenism, and expression of estrogen receptor (ER). The aim of this review was to clarify the role of ER in endometrial diseases carcinoma. The estrogens exert their effect via two estrogen receptor: α and β. The ERs modulate transcriptional process by binding directly to the estrogen response elements (ERE) located in the target gene, or in non classical mode through protein-protein tethering with other transcription factors. There are also orphan receptors (their natural ligands have not been identified). Among this group, estrogen receptor-related receptors (ERRs) were identified by their sequences similar to those of ERs. Since the ERRs have shown a high similarity in DNA binding domain with ERs can interfere with estrogen signalling strengthening the hypothesis of an estrogen-ER-ERR crosstalk. Recently, the ERs and estrogen enzymes emerge as pharmacological targets in different disorders, as well as ERRs, and they may represent the reliable biomarkers in endometrial disease.
大约70-80%的子宫内膜癌,即I型癌,与子宫内膜增生、雌激素过多症以及雌激素受体(ER)的表达有关。本综述的目的是阐明ER在子宫内膜疾病癌变中的作用。雌激素通过两种雌激素受体发挥作用:α和β。ERs通过直接与位于靶基因中的雌激素反应元件(ERE)结合,或以非经典模式通过与其他转录因子的蛋白质-蛋白质连接来调节转录过程。也存在孤儿受体(其天然配体尚未确定)。在这一组中,雌激素受体相关受体(ERRs)通过其与ERs序列相似而被鉴定出来。由于ERRs在DNA结合结构域中与ERs显示出高度相似性,可能会干扰雌激素信号传导,这强化了雌激素-ER-ERR相互作用的假说。最近,ERs和雌激素酶以及ERRs在不同疾病中成为药理学靶点,它们可能代表子宫内膜疾病中可靠的生物标志物。