Schult David, Hölsken Annett, Siegel Sonja, Buchfelder Michael, Fahlbusch Rudolf, Kreitschmann-Andermahr Ilonka, Buslei Rolf
Institute of Neuropathology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Schwabachanlage 6, 91054 Erlangen.
Department of Neurosurgery, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Schwabachanlage 6, 91054 Erlangen.
Sci Rep. 2015 Nov 23;5:16965. doi: 10.1038/srep16965.
Enhancer of zeste homolog 2 (EZH2) is a core epigenetic regulator, playing a crucial role in cell cycle regulation. The protein is known to be associated with proliferation and worse outcome in several tumor entities. In this study, we immunohistochemically investigated the expression pattern of EZH2 in a large cohort of pituitary tumors. These results were correlated with clinical features and double immunofluorescence stainings (DIS) were conducted to evaluate co-expression of EZH2 and proliferation marker Ki-67. Furthermore, we analyzed the effect of EZH2 inhibition on cell proliferation in vitro using the pituitary cell line AtT-20. While in the normal anterior pituitary EZH2 was almost absent, the cohort of tumors showed enhanced expression levels (p ≤ 0.0005). This was positively associated with Ki-67 indices (r = 0.834, p ≤ 0.0005) and DIF confirmed a predominant co-expression of both markers. In vitro experiments revealed a significant (p ≤ 0.05) decrease of tumor cell proliferation using the EZH2 inhibitor GSK126. Our results further support that epigenetic events are involved in the pathogenesis and biology of pituitary adenomas (PA). Therefore, EZH2 may function as a new potential target for therapeutic interventions in PA.
zeste 同源物 2 增强子(EZH2)是一种核心表观遗传调节因子,在细胞周期调控中发挥关键作用。已知该蛋白与多种肿瘤实体的增殖及不良预后相关。在本研究中,我们采用免疫组织化学方法研究了一大组垂体肿瘤中 EZH2 的表达模式。将这些结果与临床特征相关联,并进行双重免疫荧光染色(DIS)以评估 EZH2 与增殖标志物 Ki-67 的共表达情况。此外,我们使用垂体细胞系 AtT-20 在体外分析了 EZH2 抑制对细胞增殖的影响。在正常垂体前叶中 EZH2 几乎不存在,而肿瘤组显示出表达水平升高(p≤0.0005)。这与 Ki-67 指数呈正相关(r = 0.834,p≤0.0005),双重免疫荧光染色证实这两种标志物主要共表达。体外实验显示,使用 EZH2 抑制剂 GSK126 可使肿瘤细胞增殖显著降低(p≤0.05)。我们的结果进一步支持表观遗传事件参与垂体腺瘤(PA)的发病机制和生物学过程。因此,EZH2 可能作为 PA 治疗干预的一个新的潜在靶点。