Comprehensive analysis of peroxiredoxins expression profiles and prognostic values in breast cancer

被引:28
作者
Mei, Jie [1 ]
Hao, Leiyu [2 ]
Liu, Xiaorui [3 ]
Sun, Guangshun [4 ]
Xu, Rui [2 ]
Wang, Huiyu [1 ]
Liu, Chaoying [1 ]
机构
[1] Nanjing Med Univ, Wuxi Peoples Hosp, Dept Oncol, Wuxi 214023, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Physiol, Nanjing 211166, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Sch Pediat, Nanjing 211166, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Wuxi Peoples Hosp, Dept Gen Surg, Wuxi 214023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
PRDX; Bioinformatic analysis; Gene expression; Prognostic; Breast cancer; MESSENGER-RNA EXPRESSION; OXIDATIVE STRESS; GENE-EXPRESSION; SURVIVAL; OVEREXPRESSION; PEROXIDASE; APOPTOSIS; SUBTYPES; ROLES; CELLS;
D O I
10.1186/s40364-019-0168-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The peroxiredoxins (PRDXs) gene family has been demonstrated to participate in carcinogenesis and development of numerous cancers and the prognostic values in several cancers have been evaluated already. Purpose of our research is to explore the expression profiles and prognostic values of PRDXs in breast cancer (BrCa). Methods The transcriptional levels of PDRX family members in primary BrCa tissues and their association with intrinsic subclasses were analyzed using UALCAN database. Then, the genetic alterations of PDRXs were examined by cBioPortal database. Moreover, the prognostic values of PRDXs in BrCa patients were investigated via the Kaplan-Meier plotter. Results The transcriptional levels of most PRDXs family members in BrCa tissues were significantly elevated compared with normal breast tissues. Meanwhile, dysregulated PRDXs expression was associated with intrinsic subclasses of BrCa. Besides, copy number alterations (CNA) of PRDXs positively regulated their mRNA expressions. Furthermore, high mRNA expression of PRDX4/6 was significantly associated with poor overall survival (OS) in BrCa patients, while high mRNA expression of PRDX3 was notably related to favorable OS. Simultaneously, high mRNA expression of PRDX1/2/4/5/6 was significantly associated with shorter relapse-free survival (RFS) in BrCa patients, while high mRNA expression of PRDX3 was notably related to favorable RFS. In addition, the prognostic value of PRDXs in the different clinicopathological features based on intrinsic subclasses and chemotherapeutic treatment of BrCa patients was further assessed in the KM plotter database. Conclusion Our findings systematically elucidate the expression profiles and distinct prognostic values of PRDXs in BrCa, which might provide novel therapeutic targets and potential prognostic biomarkers for BrCa patients.
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页数:11
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