Abstract

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. 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. 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. 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. 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 the GSE9893 data set and 0.691 for 3-year survival and 0.718 for 5-year survival in the GSE42568 data set. This DRG signature mainly involved some regulation pathways of vascular endothelial cell proliferation. 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.

Highlights

  • Global Cancer Statistics 2018 estimated that 18.1 million new cases of cancer and 9.6 million cancerrelated deaths occurred globally in 2018.1 In comparison with the 1 345 680 cancer-related deaths that occurred in the United States in 2014, the total number of cancer-related deaths in this country in 2019 has been estimated to increase by approximately 4.8% (1 409 700 cancer-related deaths, including 787 800 men and 621 900 women) based on the latest cancer prediction data.[2]

  • To examine the potential mechanisms of the DNA repair–related gene (DRG), Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were performed. In this prognostic study based on samples from 1096 women with breast cancer (BC), 8 DRGs (MDC1, RPA3, MED17, DDB2, SFPQ, XRCC4, CYP19A1, and PARP3) were identified as prognostic biomarkers

  • Key Points Question Can a better prognosis model based on DNA repair–related genes be developed for the comprehensive evaluation of breast cancer?. In this prognostic study based on samples from 1096 women, a novel signature for breast cancer constructed using 8 DNA repair–related genes showed satisfactory performance for predicting survival in the training cohort from The Cancer Genome Atlas and the validation cohort from the Gene Expression Omnibus database

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Summary

Introduction

Global Cancer Statistics 2018 estimated that 18.1 million new cases of cancer and 9.6 million cancerrelated deaths occurred globally in 2018.1 In comparison with the 1 345 680 cancer-related deaths that occurred in the United States in 2014, the total number of cancer-related deaths in this country in 2019 has been estimated to increase by approximately 4.8% (1 409 700 cancer-related deaths, including 787 800 men and 621 900 women) based on the latest cancer prediction data.[2]. It is necessary to identify effective prognostic models to assess the overall survival (OS) of patients with BC and provide guidance for clinicians in early diagnosis and treatment

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