Comprehensive Analysis of Pyroptosis-Associated in Molecular Classification, Immunity and Prognostic of Glioma

被引:27
作者
Chen, Peng [1 ]
Li, Yanyan [2 ]
Li, Na [3 ]
Shen, Liangfang [3 ]
Li, Zhanzhan [3 ,4 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Orthoped, Changsha, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Dept Nursing, Changsha, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Dept Oncol, Changsha, Peoples R China
[4] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha, Peoples R China
基金
中国国家自然科学基金;
关键词
glioma; pyroptosis; prognostic signature; tumor immunity; clinical nomogram; ANGIOGENESIS; APOPTOSIS; NECROSIS; PORE;
D O I
10.3389/fgene.2021.781538
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Integrative analysis was performed in the Chinese Glioma Genome Atlas and The Cancer Genome Atlas to describe the pyroptosis-associated molecular classification and prognostic signature in glioma. Pyroptosis-related genes were used for consensus clustering and to develop a prognostic signature. The immune statuses, molecular alterations, and clinical features of differentially expressed genes were analyzed among different subclasses and risk groups. A lncRNA-miRNA-mRNA network was built, and drug sensitivity analysis was used to identify small molecular drugs for the identified genes. Glioma can be divided into two subclasses using 30 pyroptosis-related genes. Cluster 1 displayed high immune signatures and poor prognosis as well as high immune-related function scores. A prognostic signature based on 15 pyroptosis-related genes of the CGGA cohort can predict the overall survival of glioma and was well validated in the TCGA cohort. Cluster 1 had higher risk scores. The high-risk group had high immune cell and function scores and low DNA methylation of pyroptosis-related genes. The differences in pyroptosis-related gene mutations and somatic copy numbers were significant between the high-risk and low-risk groups. The ceRNA regulatory network uncovered the regulatory patterns of different risk groups in glioma. Nine pairs of target genes and drugs were identified. In vitro, CASP8 promotes the progression of glioma cells. Pyroptosis-related genes can reflect the molecular biological and clinical features of glioma subclasses. The established prognostic signature can predict prognosis and distinguish molecular alterations in glioma patients. Our comprehensive analyses provide valuable guidelines for improving glioma patient management and individualized therapy.
引用
收藏
页数:17
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