4.7 Review

Development of small molecule inhibitors/agonists targeting STING for disease

期刊

BIOMEDICINE & PHARMACOTHERAPY
卷 132, 期 -, 页码 -

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2020.110945

关键词

Stimulator of interferon genes; Disease; Innate immune response; Small molecule inhibitors; Small molecule agonists

资金

  1. Guangdong Medical University [B2019016]
  2. Administration of Traditional Chinese Medicine of Guangdong Province [20201180]
  3. Science and Technology Special Project of Zhanjiang [2019A01009]
  4. Natural Science Foundation of Guangdong Province [2016B030309002]
  5. Basic and Applied Basic Research Program of Guangdong Province [2019A1515110201]
  6. Educational Commission of Guangdong Province [4SG20138G]
  7. Fund of Southern Marine Science and Engineering GuangdongLaboratory (Zhanjiang) [ZJW-2019-007]
  8. GDNRC [[2020]038]

向作者/读者索取更多资源

Cyclic guanosine monophosphate-adenosine monophosphate synthase (cGAS)-stimulator of interferon genes (STING) signaling pathway is the primary immune response pathway in the cytoplasm. Pharmacological regulation of the STING pathway has good characteristics in both structure and function, which plays a significant role in the immunotherapy of autoimmune diseases, autoinflammatory diseases, and cancer. In this review, we summarized the activation of STING signaling pathway, the STING-related diseases, the development principle and the latest progress of inhibitors and agonists targeting STING. Our review demonstrates that STING signal pathway is a promising drug target, providing effective clues and correct guidance for the discovery of novel small molecule inhibitors/agonists that targeted STING for cancer, autoimmune, and inflammatory diseases.

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