Establishment of the Prognostic Index Reflecting Tumor Immune Microenvironment of Lung Adenocarcinoma Based on Metabolism-Related Genes

被引:22
作者
Zhang, Jianguo [1 ]
Zhang, Jianzhong [2 ]
Yuan, Cheng [1 ]
Luo, Yuan [1 ]
Li, Yangyi [1 ]
Dai, Panpan [1 ]
Sun, Wenjie [1 ]
Zhang, Nannan [1 ]
Ren, Jiangbo [3 ]
Zhang, Junhong [1 ,4 ,5 ]
Gong, Yan [3 ]
Xie, Conghua [1 ,4 ,5 ]
机构
[1] Wuhan Univ, Dept Radiat & Med Oncol, Zhongnan Hosp, 169 Donghu Rd, Wuhan 430071, Hubei, Peoples R China
[2] Qingdao Univ, Sch Publ Hlth, Dept Occupat & Environm Hlth, Qingdao 266021, Shandong, Peoples R China
[3] Wuhan Univ, Dept Biol Repositories, Zhongnan Hosp, 169 Donghu Rd, Wuhan 430071, Hubei, Peoples R China
[4] Wuhan Univ, Hubei Key Lab Tumour Biol Behav, Zhongnan Hosp, Wuhan 430071, Hubei, Peoples R China
[5] Wuhan Univ, Hubei Canc Clin Study Ctr, Zhongnan Hosp, Wuhan 430071, Hubei, Peoples R China
来源
JOURNAL OF CANCER | 2020年 / 11卷 / 24期
基金
中国国家自然科学基金;
关键词
lung adenocarcinoma; metabolic landscape; prognostic index; bioinformatics; tumor immune microenvironment; CD4(+) T-CELLS; PATIENT SURVIVAL; CANCER; EXPRESSION; MACROPHAGES; PROGRESSION; SIGNATURE; ANGIOGENESIS; INFILTRATION; MECHANISMS;
D O I
10.7150/jca.49266
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The incidence of lung adenocarcinoma ( LUAD) increased substantially in recent years. A systematic investigation of the metabolic genomics pattern is critical to improve the treatment and prognosis of LUAD. This study aimed to analyze the relationship between tumor microenvironment (TME) and metabolism-related genes of LUAD. Methods: The data was extracted from TCGA and GEO datasets. The metabolism-related gene expression profile and the corresponding clinical data of LUAD patients were then integrated. The survival-related genes were screened out using univariate COX regression and lasso regression analysis. The latent properties and molecular mechanisms of these LUAD-specific metabolism-related genes were investigated by computational biology. Results: A novel prognostic model was established based on 8 metabolism-related genes, including TYMS, ALDH2, PKM, GNPNAT1, LDHA, ENTPD2, NT5E, and MAOB. The immune infiltration of LUAD was also analyzed using CIBERSORT algorithms and TIMER database. In addition, the high- and low-risk groups exhibited distinct layout modes in the principal component analysis. Conclusions: In summary, our studies identified clinically significant metabolism-related genes, which were potential signature for LUAD diagnosis, monitoring, and prognosis.
引用
收藏
页码:7101 / 7115
页数:15
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