Center for Molecular Pathology, Department of Laboratory Medicine, Lund University, Skåne University Hospital, Malmö, Sweden.
J Transl Med. 2010 Aug 20;8:78. doi: 10.1186/1479-5876-8-78.
We recently demonstrated that increased expression of the RNA-binding protein RBM3 is associated with a favourable prognosis in breast cancer. The aim of this study was to examine the prognostic value of RBM3 mRNA and protein expression in epithelial ovarian cancer (EOC) and the cisplatin response upon RBM3 depletion in a cisplatin-sensitive ovarian cancer cell line.
RBM3 mRNA expression was analysed in tumors from a cohort of 267 EOC cases (Cohort I) and RBM3 protein expression was analysed using immunohistochemistry (IHC) in an independent cohort of 154 prospectively collected EOC cases (Cohort II). Kaplan Meier analysis and Cox proportional hazards modelling were applied to assess the relationship between RBM3 and recurrence free survival (RFS) and overall survival (OS). Immunoblotting and IHC were used to examine the expression of RBM3 in a cisplatin-resistant ovarian cancer cell line A2780-Cp70 and its cisplatin-responsive parental cell line A2780. The impact of RBM3 on cisplatin response in EOC was assessed using siRNA-mediated silencing of RBM3 in A2780 cells followed by cell viability assay and cell cycle analysis.
Increased RBM3 mRNA expression was associated with a prolonged RFS (HR = 0.64, 95% CI = 0.47-0.86, p = 0.003) and OS (HR = 0.64, 95% CI = 0.44-0.95, p = 0.024) in Cohort I. Multivariate analysis confirmed that RBM3 mRNA expression was an independent predictor of a prolonged RFS, (HR = 0.61, 95% CI = 0.44-0.84, p = 0.003) and OS (HR = 0.62, 95% CI = 0.41-0.95; p = 0.028) in Cohort I. In Cohort II, RBM3 protein expression was associated with a prolonged OS (HR = 0.53, 95% CI = 0.35-0.79, p = 0.002) confirmed by multivariate analysis (HR = 0.61, 95% CI = 0.40-0.92, p = 0.017). RBM3 mRNA and protein expression levels were significantly higher in the cisplatin sensitive A2780 cell line compared to the cisplatin resistant A2780-Cp70 derivative. siRNA-mediated silencing of RBM3 expression in the A2780 cells resulted in a decreased sensitivity to cisplatin as demonstrated by increased cell viability and reduced proportion of cells arrested in the G2/M-phase.
These data demonstrate that RBM3 expression is associated with cisplatin sensitivity in vitro and with a good prognosis in EOC. Taken together these findings suggest that RBM3 may be a useful prognostic and treatment predictive marker in EOC.
我们最近证明,RNA 结合蛋白 RBM3 的表达增加与乳腺癌的预后良好相关。本研究的目的是研究 RBM3mRNA 和蛋白表达在卵巢上皮性癌(EOC)中的预后价值,并在顺铂敏感的卵巢癌细胞系中研究 RBM3 耗竭对顺铂反应的影响。
在 267 例 EOC 病例队列(队列 I)中分析了 RBM3mRNA 的表达,在 154 例前瞻性收集的 EOC 病例队列(队列 II)中使用免疫组织化学(IHC)分析了 RBM3 蛋白的表达。应用 Kaplan-Meier 分析和 Cox 比例风险模型评估 RBM3 与无复发生存(RFS)和总生存(OS)之间的关系。免疫印迹和 IHC 用于检查顺铂耐药卵巢癌细胞系 A2780-Cp70 及其顺铂反应性亲本细胞系 A2780 中 RBM3 的表达。通过 siRNA 介导的 RBM3 沉默,在 A2780 细胞中评估 RBM3 对 EOC 中顺铂反应的影响,然后进行细胞活力测定和细胞周期分析。
队列 I 中,RBM3mRNA 表达增加与 RFS(HR = 0.64,95%CI = 0.47-0.86,p = 0.003)和 OS(HR = 0.64,95%CI = 0.44-0.95,p = 0.024)的延长相关。多变量分析证实,RBM3mRNA 表达是 RFS 延长的独立预测因子(HR = 0.61,95%CI = 0.44-0.84,p = 0.003)和 OS(HR = 0.62,95%CI = 0.41-0.95;p = 0.028)在队列 I 中。在队列 II 中,RBM3 蛋白表达与 OS 延长相关(HR = 0.53,95%CI = 0.35-0.79,p = 0.002),这一点通过多变量分析得到了证实(HR = 0.61,95%CI = 0.40-0.92,p = 0.017)。与顺铂耐药的 A2780-Cp70 衍生物相比,RBM3mRNA 和蛋白表达水平在顺铂敏感的 A2780 细胞系中明显更高。A2780 细胞中 RBM3 表达的 siRNA 介导沉默导致对顺铂的敏感性降低,这表现为细胞活力增加和 G2/M 期阻滞的细胞比例降低。
这些数据表明,RBM3 表达与体外顺铂敏感性和 EOC 预后良好相关。这些发现表明,RBM3 可能是 EOC 中有用的预后和治疗预测标志物。