Construction of a Necroptosis-Related lncRNA Signature for Predicting Prognosis and Immune Response in Kidney Renal Clear Cell Carcinoma

被引:4
|
作者
Zhang, Yue [1 ]
Zhuang, Tongtian [2 ]
Xin, Zhenlong [3 ]
Sun, Changjian [1 ]
Li, Deyang [1 ]
Ma, Nan [1 ]
Wang, Xiaoyan [1 ]
Wang, Xuning [4 ]
机构
[1] Air Force Hosp Northern Theater PLA, Dept Clin Lab, Shenyang 110042, Peoples R China
[2] Air Force Hosp Northern Theater PLA, Dept Dermatol, Shenyang 110042, Peoples R China
[3] Air Force Hosp Northern Theater PLA, Dept Dis Control & Prevent, Shenyang 110042, Peoples R China
[4] Air Force Hosp Northern Theater PLA, Dept Gen Surg, Shenyang 110042, Peoples R China
关键词
KIRC; necroptosis; lncRNA; prognosis; immune response; signature; CANCER; RIP3; PROLIFERATION; METASTASIS; EXPRESSION; MIGRATION; INVASION; COMPLEX;
D O I
10.3390/cells12010066
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Necroptosis is a new type of programmed cell death and involves the occurrence and development of various cancers. Moreover, the aberrantly expressed lncRNA can also affect tumorigenesis, migration, and invasion. However, there are few types of research on the necroptosis-related lncRNA (NRL), especially in kidney renal clear cell carcinoma (KIRC). In this study, we analyzed the sequencing data obtained from the TGCA-KIRC dataset, then applied the LASSO and COX analysis to identify 6 NRLs (AC124854.1, AL117336.1, DLGAP1-AS2, EPB41L4A-DT, HOXA-AS2, and LINC02100) to construct a risk model. Patients suffering from KIRC were divided into high- and low-risk groups according to the risk score, and the patients in the low-risk group had a longer OS. This signature can be used as an indicator to predict the prognosis of KIRC independent of other clinicopathological features. In addition, the gene set enrichment analysis showed that some tumor and immune-associated pathways were more enriched in a high-risk group. We also found significant differences between the high and low-risk groups in the infiltrating immune cells, immune functions, and expression of immune checkpoint molecules. Finally, we use the "pRRophetic" package to complete the drug sensitivity prediction, and the risk score could reflect patients' response to 8 small molecule compounds. In general, NRLs divided KIRC into two subtypes with different risk scores. Furthermore, this signature based on the 6 NRLs could provide a promising method to predict the prognosis and immune response of KIRC patients. To some extent, our findings helped give a reference for further research between NRLs and KIRC and find more effective therapeutic drugs for KIRC.
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页数:17
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