Identification of a Pyroptosis-Related Gene Signature for Predicting Overall Survival and Response to Immunotherapy in Hepatocellular Carcinoma

被引:17
|
作者
Zheng, Susu [1 ,2 ,3 ]
Xie, Xiaoying [1 ,2 ,3 ]
Guo, Xinkun [1 ]
Wu, Yanfang [1 ]
Chen, Guobin [1 ]
Chen, Xiaochun [1 ]
Wang, Meixia [1 ]
Xue, Tongchun [2 ,3 ]
Zhang, Boheng [1 ,2 ,3 ,4 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Hepat Oncol, Xiamen Branch, Xiamen, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Key Lab Carcinogenesis & Canc Invas, Chinese Minist Educ, Shanghai, Peoples R China
[3] Fudan Univ, Shanghai Med Sch, Liver Canc Inst, Shanghai, Peoples R China
[4] Fudan Univ, Ctr Evidence Based Med, Shanghai Med Sch, Shanghai, Peoples R China
关键词
pyroptosis; hepatocellular carcinoma; prognosis; immune infiltrates; immune checkpoint inhibitors; MACROPHAGES; INJURY; CELLS; DFNA5;
D O I
10.3389/fgene.2021.789296
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Pyroptosis is a novel kind of cellular necrosis and shown to be involved in cancer progression. However, the diverse expression, prognosis and associations with immune status of pyroptosis-related genes in Hepatocellular carcinoma (HCC) have yet to be analyzed. Herein, the expression profiles and corresponding clinical characteristics of HCC samples were collected from the Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. Then a pyroptosis-related gene signature was built by applying the least absolute shrinkage and selection operator (LASSO) Cox regression model from the TCGA cohort, while the GEO datasets were applied for verification. Twenty-four pyroptosis-related genes were found to be differentially expressed between HCC and normal samples. A five pyroptosis-related gene signature (GSDME, CASP8, SCAF11, NOD2, CASP6) was constructed according to LASSO Cox regression model. Patients in the low-risk group had better survival rates than those in the high-risk group. The risk score was proved to be an independent prognostic factor for overall survival (OS). The risk score correlated with immune infiltrations and immunotherapy responses. GSEA indicated that endocytosis, ubiquitin mediated proteolysis and regulation of autophagy were enriched in the high-risk group, while drug metabolism cytochrome P450 and tryptophan metabolism were enriched in the low-risk group. In conclusion, our pyroptosis-related gene signature can be used for survival prediction and may also predict the response of immunotherapy.
引用
收藏
页数:12
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