Dai Zhijun, Tian Tian, Wang Meng, Yang Tielin, Li Hongtao, Lin Shuai, Hao Qian, Xu Peng, Deng Yujiao, Zhou Linghui, Li Na, Diao Yan
1Department of Breast Surgery, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, 510623 Guangdong China.
2Department of Oncology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710004 China.
Cancer Cell Int. 2019 Jan 8;19:11. doi: 10.1186/s12935-019-0727-z. eCollection 2019.
Estrogen exposure is a widely known risk factor for BC. And the interaction of estrogen with estrogen receptor (ER) plays an important role in breast cancer development. This case-control study aims to assess the association of genetic polymorphisms in the estrogen receptor genes with breast cancer (BC) susceptibility in Chinese Han women.
Four polymorphisms (rs2881766, rs9383951, rs9340799 in and rs3020449 in ) were genotyped in 459 patients and 549 healthy controls using the Sequenom MassARRAY method. Odds ratio (OR) and 95% confidence intervals (95% CI) were calculated to evaluate the associations. False-positive report probability (FPRP) was utilized to examine the noteworthiness of significant findings.
We observed that rs2881766 was associated with a decreased BC risk (GG vs. TT: OR = 0.63, 95% CI = 0.44-0.91; GG vs. TT/GT: OR = 0.68, 95% CI = 0.49-0.95), while rs3020449 was associated with an increased risk of BC (CT vs. TT: OR = 1.58, 95% CI = 1.21-2.06; CT/CC vs. TT: OR = 1.54, 95% CI = 1.20-1.98; TT/CC vs. CT: OR = 1.48, 95% CI = 1.15-1.90). The other two polymorphisms have no relation with BC susceptibility. In addition, rs2881766 was correlated with lymph node metastasis and ER expression, and rs3020449 was related to tumor size, histological grade and ER expression. The values of false-positive report probability indicated that the significant associations of BC risk with both rs2881766 and rs3020449 were noteworthy.
Our study suggests that polymorphisms rs2881766 and rs3020449 in estrogen receptor genes were associated with BC susceptibility as well as clinical features in Chinese women. These findings need further validation in a large population.
雌激素暴露是乳腺癌(BC)广为人知的风险因素。雌激素与雌激素受体(ER)的相互作用在乳腺癌发展中起重要作用。本病例对照研究旨在评估雌激素受体基因中的基因多态性与中国汉族女性乳腺癌(BC)易感性之间的关联。
采用Sequenom MassARRAY方法对459例患者和549例健康对照进行了4种多态性( 中的rs2881766、rs9383951、rs9340799以及 中的rs3020449)的基因分型。计算优势比(OR)和95%置信区间(95%CI)以评估关联。利用假阳性报告概率(FPRP)来检验显著发现的重要性。
我们观察到rs2881766与BC风险降低相关(GG与TT:OR = 0.63,95%CI = 0.44 - 0.91;GG与TT/GT:OR = 0.68,95%CI = 0.49 - 0.95),而rs3020449与BC风险增加相关(CT与TT:OR = 1.58,95%CI = 1.21 - 2.06;CT/CC与TT:OR = 1.54,95%CI = 1.20 - 1.98;TT/CC与CT:OR = 1.48,95%CI = 1.15 -