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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

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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