Sakaguchi Hideki, Fujimoto Jiro, Sun Wen-Shu, Tamaya Teruhiko
Department of Obstetrics and Gynecology, Gifu University School of Medicine, 1-1 Yanagido, Gifu City 501-1194, Japan.
J Steroid Biochem Mol Biol. 2007 May;104(3-5):237-40. doi: 10.1016/j.jsbmb.2007.03.007. Epub 2007 Mar 15.
Estrogen is recognized as a significant modifier in the development, growth and invasion of uterine endometrial cancer. Steroid receptor coactivator-3 (SRC-3; AIB1, ACTR, RAC3, TRAM-1, and pCIP) is a member of the p160 family of coactivator for nuclear hormone receptors including estrogen receptor (ER). It is reported that SRC-3 is overexpressed in various cancers. However, SRC-3 expression manner in uterine endometrial cancer is not fully understood. In this study, we showed SRC-3 mRNA expression correlates with clinical stage, depth of myometrial invasion and dedifferentiation. The prognosis of the 25 patients with higher expression of SRC-3 mRNA in uterine endometrial cancers was extremely poor (36%), whereas the 24-month survival rate of the 15 patients with lower expression of SRC-3 mRNA was 96%. These data indicate that SRC-3 might be an important indicator of uterine endometrial cancer advancement and survival.
雌激素被认为是子宫内膜癌发生、发展和侵袭过程中的重要调节因子。类固醇受体辅激活因子-3(SRC-3;AIB1、ACTR、RAC3、TRAM-1和pCIP)是包括雌激素受体(ER)在内的核激素受体p160辅激活因子家族的成员。据报道,SRC-3在多种癌症中过表达。然而,SRC-3在子宫内膜癌中的表达方式尚未完全明确。在本研究中,我们发现SRC-3 mRNA表达与临床分期、肌层浸润深度和去分化相关。子宫内膜癌中SRC-3 mRNA高表达的25例患者预后极差(36%),而SRC-3 mRNA低表达的15例患者24个月生存率为96%。这些数据表明,SRC-3可能是子宫内膜癌进展和生存的重要指标。