Identification of necroptosis-related genes as prognostic indicators for lower-grade glioma

被引:0
|
作者
Huang, Xiaowan [1 ]
Vafaei, Somayeh [2 ]
Li, Lingxia [1 ]
Wang, Yunjiu [1 ]
Sun, Jian [1 ]
Gao, Yuzhen [3 ]
Zhang, Jue [1 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Dept Lab Med, Shuguang Hosp, Shanghai 200021, Peoples R China
[2] Iran Univ Med Sci, Fac Adv Technol Med, Dept Mol Med, Tehran, Iran
[3] Zhejiang Univ Sch Med, Dept Clin Lab, Sir Run Run Shaw Hosp, Hangzhou 310016, Zhejiang, Peoples R China
来源
AMERICAN JOURNAL OF CANCER RESEARCH | 2023年 / 13卷 / 02期
关键词
Low-grade gliomas; necroptosis; TCGA; TMB; ssGSEA; prognosis; ISOCITRATE DEHYDROGENASE 1; CLASSIFICATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this research is to develop a predictive model based on necroptosis-related genes to predict the prognosis and survival of lower grade gliomas (LGGs) efficiently. To achieve this goal, we searched for differentially expressed necrotizing apoptosis-related genes using the TCGA and CGGA databases. To construct a prognostic model, LASSO Cox and COX regression analyses were conducted on the differentially expressed genes. In this study, three genes were used to develop a prognostic model of necrotizing apoptosis, and all samples were split into high- and low-risk groups. We observed that patients with a high-risk score had a worse overall survival rate (OS) than those with a low-risk score. In the TCGA and CGGA cohorts, the nomogram plot showed a high capacity to predict overall survival of LGG patients. GSEA analysis revealed that the high-risk group was enriched for inflammatory responses, tumor-related pathways, and pathological processes. Additionally, the high-risk score was associated with invading immune cell expression. In conclusion, our predictive model based on necroptosis-related genes in LGG was shown to be effective in the diagnosis and could predict the prognosis of LGG. In addition, we identified possible targets related to necroptosis-related genes for glioma therapy in this study.
引用
收藏
页码:692 / 708
页数:17
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