PPARα suppresses growth of hepatocellular carcinoma in a high-fat diet context by reducing neutrophil extracellular trap release

We have identified PPARα and its agonists as therapeutic targets for controlling the neutrophil extracellular traps associated with high lipid metabolism. Results from preclinical models suggest that PPARα can limit mitochondrial oxidative stress, inhibit cGAS-STING-NF-κB signaling, and limit the release of neutrophil extracellular traps, thereby increasing the contact of anti-tumor leukocytes and hepatocellular cancer cells and limiting tumor growth.

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Publication Details

Journal
JHEP Reports
Published
2024-09-30
DOI
https://doi.org/10.1016/j.jhepr.2024.101228
Citations
7
Primary Topic
Peroxisome Proliferator-Activated Receptors
Type
article
Field-Weighted Citation Impact
1.64
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article

PPARα suppresses growth of hepatocellular carcinoma in a high-fat diet context by reducing neutrophil extracellular trap release

Nanhong Tang, Dongjie Ye, Banglun Pan, Haijie Hong et al.
7 citations
JHEP Reports
Peroxisome Proliferator-Activated Receptors
1.64
article

PPARα suppresses growth of hepatocellular carcinoma in a high-fat diet context by reducing neutrophil extracellular trap release

Nanhong Tang, Dongjie Ye, Banglun Pan, Haijie Hong, Yuxin Yao, Yanling Chen, Xiaoxia Zhang, Xinran Cai, Yue Luo, Zhu Zhang
article en
7 citations

Abstract

We have identified PPARα and its agonists as therapeutic targets for controlling the neutrophil extracellular traps associated with high lipid metabolism. Results from preclinical models suggest that PPARα can limit mitochondrial oxidative stress, inhibit cGAS-STING-NF-κB signaling, and limit the release of neutrophil extracellular traps, thereby increasing the contact of anti-tumor leukocytes and hepatocellular cancer cells and limiting tumor growth.

JHEP ReportsVol. 7(1)
Fujian Medical University (CN), Union Hospital (CN)
Zero hunger
Openalex Percentile: Top 16%
Peroxisome Proliferator-Activated Receptors
1.64
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