| Literature DB >> 31134613 |
Peng Sheng Yi1, Yan Shu1, Wang Xiu Bi1, Xiao Bo Zheng2, Wan Jing Feng2, Lin Ye He2, Jian Shui Li1.
Abstract
Hepatocellular carcinoma (HCC), the third leading cause of cancer-associated mortality worldwide, is a major public health problem. Zinc finger protein A20 (A20), an acute phase response gene, is a potent inhibitor of NF-κB signaling. A20 serves a critical role in liver protection, including limiting inflammation following hepatic injury, stimulating hepatocyte growth, and preventing hepatic ischemia-reperfusion injury. A20 is also involved in different processes, including tumorigenesis, progression, and metastasis through multiple mechanisms. Accumulated studies have reported the clinical implications and biological relevance of A20 in the development and progression of HCC. The underlying mechanisms of A20 in HCC include inhibition of epithelial-mesenchymal transition, protein tyrosine kinase 2 activation and Rac family GTPase 1 activity. Combining liver protection with tumor inhibition is a unique advantage of A20, which has the potential to be a novel treatment for promoting liver regeneration following liver resection in patients with HCC with liver cirrhosis. This review discusses the hepato-protective effect of A20 on hepatocytes and its potential role in cancer development, particularly its suppressor effect on HCC.Entities:
Keywords: hepatectomy; hepatocellular carcinoma; liver regeneration; suppressor; zinc finger protein A20
Mesh:
Substances:
Year: 2019 PMID: 31134613 DOI: 10.1002/jcp.28877
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384