PANoptosis-related genes function as efficient prognostic biomarkers in colon adenocarcinoma

被引:3
|
作者
Liu, Yang [1 ]
Wang, Yizhao [1 ]
Feng, Huijin [2 ]
Ma, Lianjun [1 ]
Liu, Yanqing [2 ]
机构
[1] Jilin Univ, China Japan Union Hosp, Endoscopy Ctr, Changchun, Jilin, Peoples R China
[2] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY 10027 USA
来源
FRONTIERS IN ENDOCRINOLOGY | 2024年 / 15卷
关键词
PANoptosis; prognostic model; colon adenocarcinoma; tumor immunity; tumor microenvironment; risk score; CELL-DEATH; CANCER CELLS; LINEAR-MODELS; APOPTOSIS; NECROPTOSIS; FERROPTOSIS; ACTIVATION; PYROPTOSIS; RESISTANCE; INHIBITOR;
D O I
10.3389/fendo.2024.1344058
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background PANoptosis is a newly discovered cell death type, and tightly associated with immune system activities. To date, the mechanism, regulation and application of PANoptosis in tumor is largely unknown. Our aim is to explore the prognostic value of PANoptosis-related genes in colon adenocarcinoma (COAD).Methods Analyzing data from The Cancer Genome Atlas-COAD (TCGA-COAD) involving 458 COAD cases, we concentrated on five PANoptosis pathways from the Molecular Signatures Database (MSigDB) and a comprehensive set of immune-related genes. Our approach involved identifying distinct genetic COAD subtype clusters and developing a prognostic model based on these parameters.Results The research successfully identified two genetic subtype clusters in COAD, marked by distinct profiles in PANoptosis pathways and immune-related gene expression. A prognostic model, incorporating these findings, demonstrated significant predictive power for survival outcomes, underscoring the interplay between PANoptosis and immune responses in COAD.Conclusion This study enhances our understanding of COAD's genetic framework, emphasizing the synergy between cell death pathways and the immune system. The development of a prognostic model based on these insights offers a promising tool for personalized treatment strategies. Future research should focus on validating and refining this model in clinical settings to optimize therapeutic interventions in COAD.
引用
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页数:15
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