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• W2745227329 abstract "// Yuxin Xie 1, * , Qiheng Gou 1, * , Qianqian Wang 1, * , Xiaorong Zhong 1 and Hong Zheng 1 1 Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, P. R. China * These authors have contributed equally to this work Correspondence to: Hong Zheng, email: hzheng@scu.edu.cn Keywords: BRCA, triple-negative breast cancer, prognosis, meta-analysis Received: October 05, 2016      Accepted: July 18, 2017      Published: August 03, 2017 ABSTRACT Studies have showed that dysfunction in the breast cancer susceptibility gene (BRCA) is associated with triple-negative breast cancer (TNBC); however, its effect on patient survival remains controversial. We investigated the distribution of BRCA1/2 mutations in unselected Chinese patients with TNBC and explored their roles in prognosis. Then a systematic review and meta-analysis were performed to evaluate the prognostic role of BRCA dysfunction, including BRCA1/2 germline/somatic mutations, BRCA1 promoter methylation, and low BRCA1 protein expression in TNBC patients. Pooled hazard ratios with 95% confidence intervals were estimated to determine the association between BRCA dysfunction and survival. Our results showed a high frequency of BRCA1/2 mutations, especially germline BRCA1 variants, were associated with bilateral breast cancer. Although no correlations were found between BRCA1/2 mutations and recurrence-free survival (RFS) or overall survival (OS). In the meta-analysis, patients with BRCA1 promoter methylation showed poor OS. However, there was a favorable impact on disease free survival (DFS) for TNBC patients with BRCA1 promoter methylation when received adjuvant-chemotherapy. In conclusion, BRCA1/2 mutations were associated with bilateral breast cancer and BRCA1 promoter methylation may have a prognostic effect on TNBC." @default.
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• W2745227329 date "2017-08-03" @default.
• W2745227329 modified "2023-10-16" @default.
• W2745227329 title "The role of BRCA status on prognosis in patients with triple-negative breast cancer" @default.
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• W2745227329 doi "https://doi.org/10.18632/oncotarget.19895" @default.
• W2745227329 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5675622" @default.
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