CLC number:
On-line Access: 2025-04-23
Received: 2023-09-19
Revision Accepted: 2024-04-23
Crosschecked: 2025-04-24
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Tiantian GE, Yao CHEN, Lantian PANG, Junwei SHAO, Zhi CHEN. Roles of PANoptosis and related genes in acute liver failure: neoteric insight from bioinformatics analysis and animal experiment verification[J]. Journal of Zhejiang University Science B, 2025, 26(4): 353-370.
@article{title="Roles of PANoptosis and related genes in acute liver failure: neoteric insight from bioinformatics analysis and animal experiment verification",
author="Tiantian GE, Yao CHEN, Lantian PANG, Junwei SHAO, Zhi CHEN",
journal="Journal of Zhejiang University Science B",
volume="26",
number="4",
pages="353-370",
year="2025",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B2300678"
}
%0 Journal Article
%T Roles of PANoptosis and related genes in acute liver failure: neoteric insight from bioinformatics analysis and animal experiment verification
%A Tiantian GE
%A Yao CHEN
%A Lantian PANG
%A Junwei SHAO
%A Zhi CHEN
%J Journal of Zhejiang University SCIENCE B
%V 26
%N 4
%P 353-370
%@ 1673-1581
%D 2025
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B2300678
TY - JOUR
T1 - Roles of PANoptosis and related genes in acute liver failure: neoteric insight from bioinformatics analysis and animal experiment verification
A1 - Tiantian GE
A1 - Yao CHEN
A1 - Lantian PANG
A1 - Junwei SHAO
A1 - Zhi CHEN
J0 - Journal of Zhejiang University Science B
VL - 26
IS - 4
SP - 353
EP - 370
%@ 1673-1581
Y1 - 2025
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B2300678
Abstract: BackgroundPANoptosis has the features of pyroptosis, apoptosis, and necroptosis. Numerous studies have confirmed the diverse roles of various types of cell death in acute liver failure (ALF), but limited attention has been given to the crosstalk among them. In this study, we aimed to explore the role of PANoptosis in ALF and uncover new targets for its prevention or treatment.
MethodsThree ALF-related datasets (GSE14668, GSE62029, and GSE74000) were downloaded from the gene Expression Omnibus (GEO) database to identify differentially expressed genes (DEGs). Hub genes were identified through intersecting DEGs, genes obtained from weighted gene co-expression network analysis (WGCNA), and genes related to PANoptosis. Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), protein‒protein interaction (PPI) analyses and gene set enrichment analysis (GSEA) were performed to determine functional roles. Verification was performed using an ALF mouse model.
ResultsOur results showed that expression of seven hub genes (B-cell lymphoma-2-modifying factor (BMF), B-cell lymphoma-2-interacting protein 3-like (BNIP3L), Caspase-1 (CASP1), receptor-interacting protein kinase 3 (RIPK3), uveal autoantigen with coiled-coil domains and ankyrin repeats protein (UACA), uncoordinated-5 homolog B receptor (UNC5B), and Z-DNA-binding protein 1 (ZBP1)) was up-regulated in liver samples of patients. However, in the ALF mouse model, the expression of BNIP3L, RIPK3, phosphorylated RIPK3 (P-RIPK3), UACA, and cleaved caspase-1 was up-regulated, while the expression of CASP1 and UNC5B was down-regulated. The expression of ZBP1 and BMF increased only during the development of ALF, and there was no significant change in the end stage. Immunofluorescence of mouse liver tissue showed that macrophages expressed all seven markers. Western blot results showed that pyroptosis, apoptosis, and necroptosis were always involved in lipopolysaccharide (LPS)/
ConclusionsOur results suggest that PANoptosis of macrophages promotes the development of ALF. The seven new ALF biomarkers identified and validated in this study may contribute to further investigation of diagnostic markers or novel therapeutic targets of ALF.
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