Sun Mei-Yang, Chang Xin-Zhong, Xu Gui-Ying, Dong Yi, Zhou Zi-Jun, Liu Tao, Wang Chang-Qing, Li Yong-Shuang
Department of the Second Section Office of Breast Tumor (Second Department of Breast Cancer), Jilin Cancer Hospital, Changchun 130000, P.R. China.
Department of the Second Section Office of Breast Tumor (Second Department of Breast Cancer), Tianjin Cancer Hospital, Tianjin 300000, P.R. China.
J Cancer Res Ther. 2018 Jun;14(Supplement):S354-S361. doi: 10.4103/0973-1482.235354.
The current meta-analysis investigated the correlation between breast cancer type 1 (BRCA1) promoter methylation and the clinicopathological features of breast cancer (BC).
An electronic literature search was performed to identify and select cohort studies, by employing stringent inclusion and exclusion criteria, for data relevant to promoter methylation of BRCA1 and BC. Statistical analysis of the extracted data was performed using comprehensive meta-analysis 2.0 software (CMA 2.0) (Biostat Inc., Englewood, New Jersey, USA).
A total of 125 published studies were retrieved from the literature search, and finally, 18 cohort studies meeting our inclusion criteria were incorporated into our meta-analysis. The 18 studies contained a total of 3213 BC patients. Meta-analysis results revealed that BRCA1 promoter methylation in BC patients with high and moderately differentiated tumors (I-II) was significantly lower than patients with poorly-differentiation tumors (III) (odds ratio [OR] =0.450, 95% confidence interval [95% CI] =0.241-0.838, P = 0.012). BRCA1 promoter methylation in BC patients with lymph node (LN) metastasis was significantly higher than patients without LN metastasis (OR = 2.244, 95% CI = 1.278-3.940, P = 0.005). The results of ethnicity-based subgroup analysis showed a significant difference in histological grade of BC on Asians, LN metastasis of BC in Asians and Caucasians, subtypes of BC in Caucasians, and age at diagnosis of BC patients in Caucasians (all P < 0.05).
Our meta-analysis revealed that BRCA1 promoter methylation status is linked to tumor grade and LN metastasis of BC.
本荟萃分析旨在研究乳腺癌1型(BRCA1)启动子甲基化与乳腺癌(BC)临床病理特征之间的相关性。
通过严格的纳入和排除标准进行电子文献检索,以识别和选择与BRCA1启动子甲基化和BC相关的数据的队列研究。使用综合荟萃分析2.0软件(CMA 2.0)(美国新泽西州恩格尔伍德市的Biostat公司)对提取的数据进行统计分析。
通过文献检索共检索到125项已发表的研究,最终,18项符合纳入标准的队列研究被纳入我们的荟萃分析。这18项研究共纳入3213例BC患者。荟萃分析结果显示,高分化和中分化肿瘤(I-II级)的BC患者中BRCA1启动子甲基化显著低于低分化肿瘤(III级)患者(比值比[OR]=0.450,95%置信区间[95%CI]=0.241-0.838,P=0.012)。有淋巴结(LN)转移的BC患者中BRCA1启动子甲基化显著高于无LN转移的患者(OR=2.244,95%CI=1.278-3.940,P=0.005)。基于种族的亚组分析结果显示,亚洲人BC的组织学分级、亚洲人和高加索人BC的LN转移、高加索人BC的亚型以及高加索人BC患者的诊断年龄存在显著差异(所有P<0.05)。
我们的荟萃分析表明,BRCA1启动子甲基化状态与BC的肿瘤分级和LN转移有关。