Pyroptosis-Related LncRNA Signatures Correlate With Lung Adenocarcinoma Prognosis

被引:10
作者
Huang, Hua [1 ]
Shi, Zijian [1 ]
Li, Yongwen [2 ]
Zhu, Guangsheng [1 ]
Chen, Chen [2 ]
Zhang, Zihe [1 ]
Shi, Ruifeng [1 ]
Su, Lianchun [3 ]
Cao, Peijun [1 ]
Pan, Zhenhua [2 ]
Zhang, Hongbing [1 ]
Liu, Minghui [1 ]
Liu, Hongyu [2 ,4 ]
Chen, Jun [1 ,2 ,3 ]
机构
[1] Tianjin Med Univ, Dept Lung Canc Surg, Gen Hosp, Tianjin, Peoples R China
[2] Tianjin Med Univ, Tianjin Lung Canc Inst, Tianjin Key Lab Lung Canc Metastasis & Tumor Micro, Gen Hosp, Tianjin, Peoples R China
[3] Shihezi Univ, Affiliated Hosp 1, Sch Med, Dept Thorac Surg, Shihezi, Peoples R China
[4] Univ Texas Southwestern Med Ctr Dallas, Quantitat Biomed Res Ctr, Dept Populat & Data Sci, Dallas, TX USA
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
基金
中国国家自然科学基金;
关键词
pyroptosis; lncRNA; prognosis; immune cell infiltrating; immune checkpoint; POOR-PROGNOSIS; CELL-DEATH; CANCER; METASTASIS;
D O I
10.3389/fonc.2022.850943
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundPyroptosis is a new type of programmed cell death, accompanied by an intense inflammatory response. Previous studies have shown that pyroptosis can modify long-chain non-coding RNA (lncRNA), thereby affecting the occurrence and progression of tumors. However, the underlying role of pyroptosis-related lncRNA in lung adenocarcinoma (LUAD) remains to be elucidated. Therefore, the purpose of our study was to evaluate the prognostic value of pyrolysis-related lncRNA in patients with LUAD. MethodsA total of 454 LUAD samples were downloaded from The Cancer Genome Atlas (TCGA) database. Pearson's correlation coefficient was used to identify the pyroptosis-related lncRNAs. Unsupervised consensus clustering was used to identify the various LUAD molecular subtypes. A least absolute shrinkage and selection operator (LASSO) analysis was conducted to construct a prognostic signature. ResultsAn 11-lncRNA prognostic signature out of 19 identified pyroptosis-related prognostic lncRNAs was constructed. The patients with LUAD were divided into low-risk and high-risk groups. Patients in the high-risk group had higher score values and mortality. The immune score, stromal score, and estimate score were lower in the high-risk group. The risk score was an independent predictor for OS in multivariate Cox regression analyses (HR > 1, p < 0.01). BTLA, PD-1, PD-L1, CTLA, and CD47 were lower expressed in the high-risk group. ConclusionsOur study identified an 11-pyroptosis-related lncRNA signature. These findings could further clarify the role of pyroptosis in LUAD and guide the prognosis and individualized treatment of patients.
引用
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页数:12
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