Prediction of Overall Survival Among Female Patients With Breast Cancer Using a Prognostic Signature Based on 8 DNA Repair-Related Genes

被引:24
|
作者
Zhang, Dai [1 ,2 ]
Yang, Si [1 ,2 ]
Li, Yiche [3 ]
Yao, Jia [1 ]
Ruan, Jian [4 ]
Zheng, Yi [1 ,2 ]
Deng, Yujiao [1 ,2 ]
Li, Na [1 ,2 ]
Wei, Bajin [1 ]
Wu, Ying [1 ,2 ]
Zhai, Zhen [2 ]
Lyu, Jun [5 ]
Dai, Zhijun [1 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Dept Breast Surg, Hangzhou 310003, Peoples R China
[2] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Oncol, Xian, Peoples R China
[3] Hebei Med Univ, Hosp 4, Breast Ctr Dept, Shijiazhuang, Hebei, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Dept Med Oncol, Hangzhou, Peoples R China
[5] Jinan Univ, Affiliated Hosp 1, Dept Clin Res, Guangzhou 510632, Peoples R China
关键词
EXPRESSION; DAMAGE; RESISTANCE; DIAGNOSIS; BIOMARKER; FOCUS; MDC1; RPA3;
D O I
10.1001/jamanetworkopen.2020.14622
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Importance Breast cancer (BC), a common malignant tumor, ranks first among cancers in terms of morbidity and mortality among female patients. Currently, identifying effective prognostic models has a significant association with the prediction of the overall survival of patients with BC and guidance of clinicians in early diagnosis and treatment. Objectives To identify a potential DNA repair-related prognostic signature through a comprehensive evaluation and to further improve the accuracy of prediction of the overall survival of patients with BC. Design, Setting, and Participants In this prognostic study, conducted from October 9, 2019, to February 3, 2020, the gene expression profiles and clinical data of patients with BC were collected from The Cancer Genome Atlas database. This study consisted of a training set from The Cancer Genome Atlas database and 2 validation cohorts from the Gene Expression Omnibus, which included 1096 patients with BC. A prognostic signature based on 8 DNA repair-related genes (DRGs) was developed to predict overall survival among female patients with BC. Main Outcomes and Measures Primary screening prognostic biomarkers were analyzed using univariate Cox proportional hazards regression analysis and the least absolute shrinkage and selection operator Cox proportional hazards regression. A risk model was completely established through multivariate Cox proportional hazards regression analysis. Finally, a prognostic nomogram, combining the DRG signature and clinical characteristics of patients, was constructed. To examine the potential mechanisms of the DRGs, Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were performed. Results In this prognostic study based on samples from 1096 women with BC (mean [SD] age, 59.6 [13.1] years), 8 DRGs (MDC1, RPA3, MED17, DDB2, SFPQ, XRCC4, CYP19A1, and PARP3) were identified as prognostic biomarkers. The time-dependent receiver operating characteristic curve analysis suggested that the 8-gene signature had a good predictive accuracy. In the training cohort, the areas under the curve were 0.708 for 3-year survival and 0.704 for 5-year survival. In the validation cohort, the areas under the curve were 0.717 for 3-year survival and 0.772 for 5-year survival in thedata set and 0.691 for 3-year survival and 0.718 for 5-year survival in thedata set. This DRG signature mainly involved some regulation pathways of vascular endothelial cell proliferation. Conclusions and Relevance In this study, a prognostic signature using 8 DRGs was developed that successfully predicted overall survival among female patients with BC. This risk model provides new clinical evidence for the diagnostic accuracy and targeted treatment of BC.
引用
收藏
页数:11
相关论文
共 50 条
  • [21] Identification of a DNA repair 9-gene signature for the overall survival prediction of pancreatic cancer
    Huang, Jiaxin
    Mao, Qiqi
    Sun, Xu
    ANNALS OF DIAGNOSTIC PATHOLOGY, 2022, 57
  • [22] Development and validation of a prognostic signature for preoperative prediction of overall survival in gastric cancer patients
    Zhu, Minggu
    Wang, Qicai
    Luo, Zhaowen
    Liu, Kelong
    Zhang, Zhiqiao
    ONCOTARGETS AND THERAPY, 2018, 11 : 8711 - 8722
  • [23] A novel ferroptosis-related gene signature for overall survival prediction and immune infiltration in patients with breast cancer
    Zhang, Yan
    Liang, Yiran
    Wang, Yajie
    Ye, Fangzhou
    Kong, Xiaoli
    Yang, Qifeng
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2022, 61 (06)
  • [24] Breast cancer survival prediction using seven prognostic biomarker genes
    Liu, Liu
    Chen, Zhilin
    Shi, Wenjie
    Liu, Hui
    Pang, Weiyi
    ONCOLOGY LETTERS, 2019, 18 (03) : 2907 - 2916
  • [25] Autophagy-related prognostic signature for survival prediction of triple negative breast cancer
    Yang, Qiong
    Sun, Kewang
    Xia, Wenjie
    Li, Ying
    Zhong, Miaochun
    Lei, Kefeng
    PEERJ, 2022, 10
  • [26] A novel DNA methylation-related gene signature for the prediction of overall survival and immune characteristics of ovarian cancer patients
    Sixue Wang
    Jie Fu
    Xiaoling Fang
    Journal of Ovarian Research, 16
  • [27] A novel DNA methylation-related gene signature for the prediction of overall survival and immune characteristics of ovarian cancer patients
    Wang, Sixue
    Fu, Jie
    Fang, Xiaoling
    JOURNAL OF OVARIAN RESEARCH, 2023, 16 (01)
  • [28] A signature of seven immune‐related genes predicts overall survival in male gastric cancer patients
    Xin Xu
    Yida Lu
    Youliang Wu
    Mingliang Wang
    Xiaodong Wang
    Huizhen Wang
    Bo Chen
    Yongxiang Li
    Cancer Cell International, 21
  • [29] A novel ferroptosis-related gene signature for overall survival prediction in patients with gastric cancer
    Fang Wen
    Fan Zhao
    Wenjie Huang
    Yan Liang
    Ruolan Sun
    Yize Lin
    Weihua Zhang
    Scientific Reports, 14
  • [30] A novel ferroptosis-related gene signature for overall survival prediction in patients with gastric cancer
    Wen, Fang
    Zhao, Fan
    Huang, Wenjie
    Liang, Yan
    Sun, Ruolan
    Lin, Yize
    Zhang, Weihua
    SCIENTIFIC REPORTS, 2024, 14 (01)