Stat2 stability regulation: an intersection between immunity and carcinogenesis

被引:36
|
作者
Lee, Cheol-Jung [1 ]
An, Hyun-Jung [1 ]
Cho, Eun Suh [2 ]
Kang, Han Chang [1 ]
Lee, Joo Young [1 ]
Lee, Hye Suk [1 ]
Cho, Yong-Yeon [1 ]
机构
[1] Catholic Univ Korea, Coll Pharm, 43 Jibong Ro, Bucheon Si 14662, Gyeonggi Do, South Korea
[2] Univ Minnesota, Coll Biol Sci, 3-104 MCB 420,Washington Ave SE, Minneapolis, MN 55455 USA
来源
EXPERIMENTAL AND MOLECULAR MEDICINE | 2020年 / 52卷 / 09期
关键词
INTERFERON-ALPHA RECEPTOR; GROWTH-FACTOR RECEPTOR; INDUCED NUCLEAR IMPORT; DNA-BINDING; TRANSCRIPTIONAL ACTIVATOR; CONSTITUTIVE ACTIVATION; SIGNAL-TRANSDUCER; GAMMA-INTERFERON; TYROSINE KINASE; LINKER DOMAIN;
D O I
10.1038/s12276-020-00506-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer: Significance of stability of regulatory protein The activity of STAT2, a protein stimulated by molecular signalling systems to activate selected genes in ways that can lead to cancer, is regulated by factors controlling its rate of degradation. Yong-Yeon Cho and colleagues at The Catholic University of Korea in South Korea review the role of STAT2 in links between molecular signals of the immune response and the onset of cancer. They focus on the significance of factors that regulate the stability of STAT2. One key factor appears to be the molecular mechanisms controlling the degradation of STAT2 by cellular structures called proteasomes. These structures break down proteins as part of routine cell maintenance. Deeper understanding of the stimulation, action and degradation of STAT2 will assist efforts to treat the many cancers in which STAT2 activity is involved. Signal transducer and activator of transcription (STAT2) is a member of the STAT family that plays an essential role in immune responses to extracellular and intracellular stimuli, including inflammatory reactions, invasion of foreign materials, and cancer initiation. Although the majority of STAT2 studies in the last few decades have focused on interferon (IFN)-alpha/beta (IFN alpha/beta) signaling pathway-mediated host defense against viral infections, recent studies have revealed that STAT2 also plays an important role in human cancer development. Notably, strategic research on STAT2 function has provided evidence that transient regulatory activity by homo- or heterodimerization induces its nuclear localization where it to forms a ternary IFN-stimulated gene factor 3 (ISGF3) complex, which is composed of STAT1 and/or STAT2 and IFN regulatory factor 9 (IEF9). The molecular mechanisms of ISGF3-mediated ISG gene expression provide the basic foundation for the regulation of STAT2 protein activity but not protein quality control. Recently, previously unknown molecular mechanisms of STAT2-mediated cell proliferation via STAT2 protein quality control were elucidated. In this review, we briefly summarize the role of STAT2 in immune responses and carcinogenesis with respect to the molecular mechanisms of STAT2 stability regulation via the proteasomal degradation pathway.
引用
收藏
页码:1526 / 1536
页数:11
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