Identification of endoplasmic reticulum stress-related lncRNAs in lung adenocarcinoma by bioinformatics and experimental validation

被引:4
|
作者
Xin, Tong [1 ]
Sun, Yue [1 ]
Meng, Hongxue [2 ]
Zhang, Ningzhi [1 ]
Peng, Bo [3 ]
Yang, Xinxin [4 ]
Hu, Jing [1 ,5 ]
Cao, Mengru [1 ,5 ]
机构
[1] Harbin Med Univ, Canc Hosp, Dept Med Oncol 4, Harbin, Peoples R China
[2] Harbin Med Univ, Canc Hosp, Dept Pathol, Harbin, Peoples R China
[3] Harbin Med Univ, Affiliated Hosp 2, Dept Thorac Surg, Harbin, Peoples R China
[4] Harbin Med Univ, Canc Hosp, Precis Med Ctr, Harbin, Peoples R China
[5] Harbin Med Univ, Canc Hosp, Dept Breast Med oncol, 150 Haping Rd, Harbin, Peoples R China
基金
中国国家自然科学基金;
关键词
Endoplasmic reticulum stress; prognosis; LncRNAs; lung adenocarcinoma; TUMOR MUTATIONAL BURDEN; HEPATOCELLULAR-CARCINOMA; PROMOTES; CANCER; TUMORIGENESIS; GROWTH;
D O I
10.1080/07853890.2023.2251500
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Endoplasmic reticulum stress (ERs) is an important cellular self-defence mechanism, which is closely related to tumorigenesis and development. However, the role of endoplasmic reticulum stress state in the development of lung adenocarcinoma (LUAD) has not been clarified.Methods: The lncRNAs associated with endoplasmic reticulum stress were identified by co-expression analysis in public databases, and by the least absolute shrinkage and selection operator (LASSO) regression and multivariate Cox regression modelling, we constructed a prognostic model based on endoplasmic reticulum stress-related lncRNAs (ERs-related lncRNAs), performed immune analysis, TME, TMB and clinical drug prediction for model-related risk scores, and performed correlation validation in public databases and at the human tissue level.Results: Five ERs-related lncRNAs were used to construct an ERs-related lncRNA signature (ERs-related LncSig), which can predict the prognosis of LUAD. Patients in the high-risk group had worse survival, and differences existed in immune cell infiltration, immune function, immune checkpoint analysis, tumour microenvironment (TME), tumour mutational burden (TMB), immunotherapy efficacy, and sensitivity to some commonly used chemotherapeutic agents between high and low risk groups.Conclusion: Our study demonstrated that ERs-related lncRNA signature can be used for the prognostic evaluation of LUAD patients and may provide new insights into clinical decision-making and personalised medicine for LUAD.
引用
收藏
页数:18
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