Development of prognostic index based on autophagy-related genes analysis in breast cancer

被引:34
作者
Lin, Qing-Guang [1 ]
Liu, Wei [2 ]
Mo, Yu-Zhen [3 ]
Han, Jing [1 ]
Guo, Zhi-Xing [1 ]
Zheng, Wei [1 ]
Wang, Jian-Wei [1 ]
Zou, Xue-Bin [1 ]
Li, An-Hua [1 ]
Han, Feng [1 ]
机构
[1] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, Dept Ultrasound, State Key Lab Oncol South China,Canc Ctr, Guangzhou 510060, Guangdong, Peoples R China
[2] Jinan Univ, Guangzhou Red Cross Hosp, Med Coll, Dept Breast, Guangzhou 510220, Guangdong, Peoples R China
[3] Jinan Univ, Guangzhou Red Cross Hosp, Med Coll, Dept Radiotherapy, Guangzhou 510220, Guangdong, Peoples R China
来源
AGING-US | 2020年 / 12卷 / 02期
关键词
autophagy-related genes; breast cancer; prognosis; STATISTICS;
D O I
10.18632/aging.102687
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Autophagy is a self-digesting process that can satisfy the metabolic needs of cells, and is closely related to development of cancer. However, the effect of autophagy-related genes (ARGs) on the prognosis of breast cancer remains unclear. Results: We first found that 27 ARGs were significantly associated with overall survival in breast cancer. The prognosis-related ARGs signature established using the Cox regression model consists of 12 ARGs that can be divided patients into high-risk and low-risk groups. The overall survival of patients with high-risk scores (HR 3.652, 2.410-5.533; P < 0.001) was shorter than patients with low-risk scores. The area under the receiver operating characteristic (ROC) curve for 1-year, 3-year, and 5-year survival rates were 0.739, 0.727, and 0.742, respectively. Conclusion: The12-ARGs marker can predict the prognosis of breast cancer and thus help individualized treatment of patients at different risks. Methods: Based on the TCGA dataset, we integrated the expression profiles of ARGs in 1,039 breast cancer patients. Differentially expressed ARGs and survival-related ARGs were evaluated by computational difference algorithm and COX regression analysis. In addition, we also explored the mutations in these ARGs. A new prognostic indicator based on ARGs was developed using multivariate COX analysis.
引用
收藏
页码:1366 / 1376
页数:11
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