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NETosis in tumour microenvironment of liver: From primary to metastatic hepatic carcinoma.

Authors :
Yang Y
Yu S
Lv C
Tian Y
Source :
Ageing research reviews [Ageing Res Rev] 2024 Jun; Vol. 97, pp. 102297. Date of Electronic Publication: 2024 Apr 09.
Publication Year :
2024

Abstract

Background: Hepatocellular carcinoma is a common and highly lethal tumour. The tumour microenvironment (TME) plays an important role in the progression and metastasis of hepatocellular carcinoma (HCC). A cell death mechanism, termed NETosis, has been found to play an important role in the TME of HCC.<br />Summary: This review article focuses on the role of NETosis in the TME of HCC, a novel form of cell death in which neutrophils capture and kill microorganisms by releasing a type of DNA meshwork fibres called "NETs". This process is associated with neutrophil activation, local inflammation and cytokines. The study suggests that NETs play a multifaceted role in the development and metastasis of HCC. The article also discusses the role of NETs in tumour proliferation and metastasis, epithelial-mesenchymal transition (EMT), and surgical stress. In addition, the article discusses the interaction of NETosis with other immune cells in the TME and related therapeutic strategies. A deeper understanding of NETosis can help us better understand the complexity of the immune system and provide a new therapeutic basis for the treatment and prevention of HCC.<br />Key Information: In conclusion, NETosis is important in the TME of liver. NETs have been shown to contribute to the progression and metastasis of liver cancer. The interaction between NETosis and immune cells in the TME, as well as related therapies, are important areas of research.<br />Competing Interests: Declaration of Competing Interest The authors have no conflicts of interest to declare.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-9649
Volume :
97
Database :
MEDLINE
Journal :
Ageing research reviews
Publication Type :
Academic Journal
Accession number :
38599524
Full Text :
https://doi.org/10.1016/j.arr.2024.102297