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2000
Volume 22, Issue 4
  • ISSN: 1568-0096
  • E-ISSN: 1873-5576

Abstract

Objective: Cutaneous T cell lymphoma (CTCL) is a kind of extranodal non-Hodgkin Tcell lymphoma without healable treatment in the clinic. JAK2 amplification in CTCL patients makes it a potential target for CTCL treatment. In the present study, we aimed to evaluate the anticancer effect of ND-16, a novel nilotinib derivate, on CTCL cells and the underlying mechanism targeting JAK2. Methods and Results: We found that ND-16 was capable of regulating JAK2 and had a selective inhibitory effect on CTCL H9 cells. The surface plasmon resonance and molecular docking study indicated ND-16 bound to JAK2 with a high binding affinity. Further investigation revealed that ND-16 inhibited the downstream cascades of JAK2, including STATs, PI3K/AKT/mTOR, and MAPK pathways, followed by regulation of Bcl-2 family members and cell cycle proteins CDK/- Cyclins. Flow cytometry analysis confirmed these results that ND-16-treated H9 cells showed cell apoptosis and cell cycle arrest at S-phase. Conclusion: ND-16 may be of value in a potential therapy for the management of CTCL.

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/content/journals/ccdt/10.2174/1568009622666220225121009
2022-04-01
2025-06-21
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  • Article Type:
    Research Article
Keyword(s): apoptosis; Cutaneous T-cell lymphoma; growth; JAK2; ND-16; novel compound
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