Sheng Xianneng, Guo Yu, Lu Yang
Department of Thyroid and Breast Surgery, Ningbo First Hospital Medical School of Ningbo University, Ningbo, Zhejiang, China.
Medicine (Baltimore). 2017 Jul;96(28):e7476. doi: 10.1097/MD.0000000000007476.
BRCA1 and RASSF1A promoter methylation has been reported to be correlated with a worse survival in patients with breast cancer. However, the prognostic values of GSTP1, p16, ESR1, and PITX2 promoter methylation in breast cancer remain to be determined. Here, we performed this study to evaluate the prognostic significance of GSTP1, p16, ESR1, and PITX2 promoter methylation in breast cancer.
A range of online databases was systematically searched to identify available studies based on the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guideline. The pooled hazard ratios (HRs) with their 95% confidence intervals (95% CIs) were applied to estimate the prognostic effect of GSTP1, p16, ESR1, and PITX2 promoter methylation in breast cancer for multivariate regression analysis.
13 eligible articles involving 3915 patients with breast cancer were analyzed in this meta-analysis. In a large patient population, GSTP1 showed a trend toward a worse prognosis in overall survival (OS) (HR = 1.64, 95% CI = 0.93-2.87, P = .085). PITX2 promoter methylation was significantly correlated with a worse prognosis in OS (HR = 1.57, 95% CI = 1.15-2.14, P = .004), but no association between p16 promoter methylation and OS (HR = 0.92, 95% CI = 0.31-2.71, P = .884). PITX2 promoter methylation was significantly correlated with an unfavorable prognosis of patients with breast cancer in metastasis-free survival (MFS) (HR = 1.73, 95% CI = 1.33-2.26, P < .001). The result from 3 studies with 227 cases showed that ESR1 promoter methylation was linked to a worse prognosis in OS (HR = 1.55, 95% CI = 1.06-2.28, P = .025).
Our findings suggest ESR1 and PITX2 promoter methylation may be correlated with a worse survival of patients with breast cancer (ESR1: OS, PITX2: OS and MFS). The clinical utility of aberrantly methylated ESR1 and PITX2 could be a promising factor for the prognosis of breast cancer.
据报道,BRCA1和RASSF1A启动子甲基化与乳腺癌患者较差的生存率相关。然而,GSTP1、p16、ESR1和PITX2启动子甲基化在乳腺癌中的预后价值仍有待确定。在此,我们进行了这项研究,以评估GSTP1、p16、ESR1和PITX2启动子甲基化在乳腺癌中的预后意义。
根据系统评价和Meta分析的首选报告项目(PRISMA)指南,系统检索一系列在线数据库,以识别可用的研究。采用合并风险比(HR)及其95%置信区间(95%CI)来估计GSTP1、p16、ESR1和PITX2启动子甲基化在乳腺癌中的预后效应,用于多变量回归分析。
本Meta分析纳入了13篇符合条件的文章,共3915例乳腺癌患者。在大量患者群体中,GSTP1在总生存期(OS)方面显示出预后较差的趋势(HR = 1.64,95%CI = 0.93 - 2.87,P = 0.085)。PITX2启动子甲基化与OS较差的预后显著相关(HR = 1.57,95%CI = 1.15 - 2.14,P = 0.004),但p16启动子甲基化与OS之间无关联(HR = 0.92,95%CI = 0.31 - 2.71,P = 0.884)。PITX2启动子甲基化与乳腺癌患者无远处转移生存期(MFS)的不良预后显著相关(HR = 1.73,95%CI = 1.33 - 2.26,P < 0.001)。来自3项研究共227例病例的结果显示,ESR1启动子甲基化与OS较差的预后相关(HR = 1.55,95%CI = 1.06 - 2.28,P =