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Design, Synthesis and Structure-Activity Relationship Studies of Meridianin Derivatives as Novel JAK/STAT3 Signaling Inhibitors.

Abstract
Hyperactivation of Janus kinase (JAK)/signal transducer and activator of transcription 3 (STAT3) signaling is an attractive therapeutic target for tumor therapy. Herein, forty-eight novel meridianin derivatives were designed and synthesized, and their antitumor activity was evaluated in vitro both for activity optimization and structure-activity relationship (SAR) study. The results indicated that most derivatives exhibited significantly improved antitumor activity, especially for compound 6e. The compound 6e contains an isothiouronium linked by an alkyl chain consisting of six carbon atoms with IC50 ranging from 1.11 to 2.80 μM on various cancer cell lines. Consistently, the 6e dose dependently induced the apoptosis of A549 and DU145 cells, in which STAT3 is constitutively active. Western blotting assays indicated that the phosphorylation levels of JAK1, JAK2 and STAT3 were inhibited by 6e at 5 μM without significant change in the total STAT3 level. Moreover, 6e also suppressed the expression of STAT3 downstream genes, including c-Myc, Cyclin D1 and Bcl-XL at 10 μM. An additional in vivo study revealed that 6e at the dose of 10 mg/kg could potently inhibit the DU145 xenograft tumor without obvious body weight loss. These results clearly indicate that 6e could be a potential antitumor agent by targeting the JAK/STAT3 signaling pathway.
AuthorsJian-Qiang Zhang, Rui Li, Xue-Yang Dong, Na He, Rui-Juan Yin, Meng-Ke Yang, Jie-Yu Liu, Ri-Lei Yu, Chen-Yang Zhao, Tao Jiang
JournalInternational journal of molecular sciences (Int J Mol Sci) Vol. 23 Issue 4 (Feb 16 2022) ISSN: 1422-0067 [Electronic] Switzerland
PMID35216314 (Publication Type: Journal Article)
Chemical References
  • Indole Alkaloids
  • Janus Kinase Inhibitors
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Janus Kinase 1
  • Janus Kinase 2
Topics
  • Apoptosis
  • Cell Line, Tumor
  • Cell Proliferation
  • Humans
  • Indole Alkaloids (chemistry, pharmacology)
  • Janus Kinase 1 (antagonists & inhibitors)
  • Janus Kinase 2 (antagonists & inhibitors)
  • Janus Kinase Inhibitors (chemistry, pharmacology)
  • Phosphorylation
  • STAT3 Transcription Factor (antagonists & inhibitors)
  • Signal Transduction
  • Structure-Activity Relationship

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