NF-κB and STAT3 - key players in liver inflammation and cancer

被引:927
作者
He, Guobin [1 ]
Karin, Michael [1 ]
机构
[1] Univ Calif San Diego, Sch Med, Lab Gene Regulat & Signal Transduct, La Jolla, CA 92093 USA
关键词
NF-kappa B; STAT3; signaling transduction; inflammation; carcinogenesis; liver cancer; HCC; COLITIS-ASSOCIATED CANCER; HEPATOCELLULAR-CARCINOMA; EMBRYONIC LETHALITY; IKK-BETA; DEFICIENT MICE; HEPATITIS-C; TNF-ALPHA; CHEMICAL HEPATOCARCINOGENESIS; COMPENSATORY PROLIFERATION; REVERSIBLE ACETYLATION;
D O I
10.1038/cr.2010.183
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hepatocellular carcinoma (HCC), the major form of primary liver cancer, is one of the most deadly human cancers. The pathogenesis of HCC is frequently linked with continuous hepatocyte death, inflammatory cell infiltration and compensatory liver regeneration. Understanding the molecular signaling pathways driving or mediating these processes during liver tumorigenesis is important for the identification of novel therapeutic targets for this dreadful disease. The classical IKK beta-dependent NF-kappa B signaling pathway has been shown to promote hepatocyte survival in both developing and adult livers. In addition, it also plays a crucial role in liver inflammatory responses by controlling the expression of an array of growth factors and cytokines. One of these cytokines is IL-6, which is best known for its role in the liver acute phase response. IL-6 exerts many of its functions via activation of STAT3, a transcription factor found to be important for HCC development. This review will focus on recent studies on the roles of NF-kappa B and STAT3 in liver cancer. Interactions between the two pathways and their potential as therapeutic targets will also be discussed.
引用
收藏
页码:159 / 168
页数:10
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