4.5 Review

The spleen tyrosine kinase (SYK): A crucial therapeutic target for diverse liver diseases

期刊

HELIYON
卷 8, 期 12, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.heliyon.2022.e12130

关键词

Spleen tyrosine kinase (SYK); Liver diseases; Small molecule inhibitor; Therapy target

资金

  1. The Young Talent Support Plan of Xi'an Jiaotong University
  2. National Natural Science Foundation of China [31900547]
  3. Introducing overseas high-level talent intelligence projects of Xi'an City [2022JH-GCRC-0063]
  4. Medical Base-Clinic Integrated Innovation Project of Xi'an Jiaotong University

向作者/读者索取更多资源

Spleen tyrosine kinase (SYK) plays an important role in liver diseases by regulating signal transduction in various cells, including both hematopoietic and non-hematopoietic cells. Inhibition of SYK activity has been identified as a promising therapeutic strategy, and both hepatic and non-hepatic SYK could be potential targets for treatment. Further research is needed to better understand the significance of SYK in liver diseases and to establish more reliable treatment modes.
Spleen tyrosine kinase (SYK) is an enigmatic protein tyrosine kinase, and involved in signal transduction related with lots of cellular processes. It's highly expressed in the cells of hematopoietic origin and acts as an important therapeutic target in the treatment of autoimmune diseases and allergic disorders. In recent years, more and more evidences indicate that SYK is expressed in non-hematopoietic cells and effectively regulates various non-immune biological responses as well. In this review, we mainly summary the role of SYK in different liver diseases. Robust SYK expression has been discovered in hepatocytes, hepatic stellate cells, as well as Kupffer cells, which participates in the regulation of numerous signal transduction in various liver diseases (e.g. hepatitis, liver fibrosis and hepatocellular carcinoma). In addition, the blockage of SYK activity using small molecule modulators is considered as a significant therapeutic strategy against liver diseases, and both hepatic SYK and non-hepatic SYK could become highly promising therapeutic targets. Totally, even though some critical points about the significance of SYK in liver diseases treatment still need further elaboration, more reliable biotechnical or pharmacological therapy modes will be established based on the better understanding of the relationship between SYK and liver diseases.

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