Institute of Biology, Medicinal Chemistry & Biotechnology, National Hellenic Research Foundation, 48 Vassileos Constantinou Av, 11635 Athens, Greece.
Laboratory of Histology & Embryology, Medical School, University of Athens, 75 M. Asias str., 11527 Athens, Greece.
Cancer Lett. 2015 Mar 1;358(1):37-42. doi: 10.1016/j.canlet.2014.12.022. Epub 2014 Dec 15.
Our purpose was to assess whether and how ERβ1 and/or ERβ2 expression status could predict response of early stage ERα-positive breast carcinoma to adjuvant endocrine therapy (AET). ERβ1 and ERβ2 expression were determined using immunohistochemistry. ERβ1- and ERβ2-positivity were derived from receiver operating characteristic analysis and the median percentage of immunostained tumor cells, respectively. Patients with recurrent disease were grouped according to whether they relapsed within 4 years or after 4 years from surgery. The predictive significance of ERβ1 and ERβ2 was determined using Kaplan-Meier survival analysis and Cox proportional hazards regression analysis. ERβ1-positivity in the first-4-year relapse patient group was lower and ERβ2-positivity in the post-4-year relapse group was higher compared with no-relapse group. ERβ1-positivity was associated with lower tumor size and longer first-4-year disease-free survival, while ERβ2-positivity was associated with shorter post-4-year disease-free survival. Cox multivariate analysis including ERβ1, ERβ2 and established clinico-pathological variables showed that ERβ1-positivity was an independent predictor of lower first-4-year risk of relapse. Thus, low ERβ1 expression and high ERβ2 expression are markers for identification of AET-treated ERα-positive breast carcinoma patients at risk of early and late relapse, respectively.
我们的目的是评估 ERβ1 和/或 ERβ2 的表达状态是否以及如何预测早期 ERα 阳性乳腺癌对辅助内分泌治疗(AET)的反应。使用免疫组织化学法测定 ERβ1 和 ERβ2 的表达。ERβ1 和 ERβ2 的阳性结果分别来自接受者操作特征分析和免疫染色肿瘤细胞的中位数百分比。根据术后 4 年内或 4 年后复发的情况将复发患者分为两组。使用 Kaplan-Meier 生存分析和 Cox 比例风险回归分析确定 ERβ1 和 ERβ2 的预测意义。与无复发组相比,4 年内复发患者组的 ERβ1 阳性率较低,4 年后复发组的 ERβ2 阳性率较高。ERβ1 阳性与肿瘤体积较小和 4 年内无病生存时间较长相关,而 ERβ2 阳性与 4 年后无病生存时间较短相关。包括 ERβ1、ERβ2 和既定临床病理变量的 Cox 多变量分析表明,ERβ1 阳性是 4 年内复发风险较低的独立预测因子。因此,低 ERβ1 表达和高 ERβ2 表达分别是识别接受 AET 治疗的 ERα 阳性乳腺癌患者早期和晚期复发风险的标志物。