A JAK tyrosine kinase and pseudokinase Co-inhibition strategy combines enhanced potency and on-demand activation

Xuetao Chen, Liangying Zhang, Qichao Bao, Fanying Meng, Chihong Liu, Rujun Xu, Xinrui Ji, Qidong You, Zhengyu Jiang

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Janus tyrosine kinase (JAK) inhibitors have been on the market for several years, but their use is limited by drug resistance and intolerable side effects. Herein, we propose a novel strategy of JAK tyrosine kinase (TK) and pseudokinase (PK) domain co-inhibition system to consolidate robust JAK inhibition and on-demand activation. A photoexcited prodrug PAT-SIL-TG-1&AT exhibits the synergy effects of TK-PK co-inhibition and enable the spatiotemporal control of JAK2 signaling. The hypoxia-activated prodrug HAT-SIL-TG-1&AT significantly inhibited HEL cells proliferation and downregulated phosphorylated STAT3/5 under hypoxic conditions. Importantly, HAT-SIL-TG-1&AT showed synergistic antitumor effects and selectively inhibited the JAK-STAT signaling in tumor tissues in vivo. This work demonstrates a viable solution to achieve superior JAK2 inhibition, and provides an inspiration for other kinases containing PK domain.

Original languageEnglish (US)
Article number115198
JournalEuropean journal of medicinal chemistry
Volume250
DOIs
StatePublished - Mar 15 2023
Externally publishedYes

Keywords

  • Co-inhibition
  • JAK
  • Produrg
  • Pseudokinase
  • Tyrosine kinase

ASJC Scopus subject areas

  • Pharmacology
  • Drug Discovery
  • Organic Chemistry

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