Exploration of epithelial-mesenchymal transition-related lncRNA signature and drug sensitivity in breast cancer

被引:6
|
作者
Li, Chengxin [1 ]
Zheng, Lewei [1 ]
Xu, Gaoran [1 ]
Yuan, Qianqian [1 ]
Di, Ziyang [2 ,3 ]
Yang, Yalong [1 ]
Dong, Xingxing [1 ]
Hou, Jinxuan [1 ]
Wu, Gaosong [1 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Dept Thyroid & Breast Surg, Wuhan, Peoples R China
[2] Wuhan Univ, Zhongnan Hosp, Dept Gastrointestinal Surg, Wuhan, Peoples R China
[3] Wuhan Univ, Zhongnan Hosp, Dept Gastr & Colorectal Surg Oncol, Wuhan, Peoples R China
来源
关键词
epithelial-mesenchymal transition; breast cancer; long non-coding RNA; prognostic model; drug sensitivity; MOLECULAR-MECHANISMS; GASTRIC-CANCER; METASTASIS; EMT; DOXORUBICIN; INHIBITION; RESISTANCE; CELLS;
D O I
10.3389/fendo.2023.1154741
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundBreast cancer (BRCA) has become the most diagnosed cancer worldwide for female and seriously endanger female health. The epithelial-mesenchymal transition (EMT) process is associated with metastasis and drug resistance in BRCA patients. However, the prognostic value of EMT-related lncRNA in BRCA still needs to be revealed. The aim of this study is to construct an EMT-related lncRNA (ERL) signature with accuracy predictive ability for the prognosis of BRCA patients. MethodsRNA-seq expression data and Clinical characteristics obtained from the TCGA (The Cancer Genome Atlas) were used in the study. First, we identified the EMT-related lncRNA by the Pearson correlation analysis. An EMT-related lncRNAs prognostic risk signature was constructed using univariate Cox regression and Lasso-penalized Cox regression analyses. The model's performance was validated using Kaplan-Meier (KM) survival analysis, ROC curve and C-index. Finally, a nomogram was constructed for clinical practice in evaluating the patients with BRCA and validated by calibration curve and decision curve analysis (DCA). We also evaluated the drug sensitivity of signature lncRNA and the tumor immune cell infiltration in breast cancer. ResultsWe constructed a 10-lncRNA risk score signature based on the lncRNAs associated with the EMT process. We could assign BRCA patients to the high- and low-risk group according to the median risk score. The prognostic risk signature showed excellent accuracy and demonstrated sufficient independence from other clinical characteristics. The immune cell infiltration analysis showed that the prognostic risk signature was related to the infiltration of the immune cell subtype. Drug sensitivity analysis proved ERLs signature could effectively predict the sensitivity of patients to common chemotherapy drugs in BRCA and provide guidance for chemotherapy drugs for high-risk and low-risk patients. ConclusionOur ERL signature and nomogram have excellent prognostic value and could become reliable tools for clinical guidance.
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页数:13
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