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Targeting p97-Npl4 interaction inhibits tumor T reg cell development to enhance tumor immunity.

Pingping NieZhifa CaoRuixian YuChao DongWeihong ZhangYan MengHui ZhangYu PanZhenzhu TongXiaoya JiangShilong WangMengwen ZhuYi HanWenjia WangYiming ZhangLijie TanChuanchuan LiYuanzhi XuLiwei AnBin LiShi JiaoZhaocai Zhou
Published in: Nature immunology (2024)
Targeting tumor-infiltrating regulatory T (TI-T reg ) cells is a potential strategy for cancer therapy. The ATPase p97 in complex with cofactors (such as Npl4) has been investigated as an antitumor drug target; however, it is unclear whether p97 has a function in immune cells or immunotherapy. Here we show that thonzonium bromide is an inhibitor of the interaction of p97 and Npl4 and that this p97-Npl4 complex has a critical function in TI-T reg cells. Thonzonium bromide boosts antitumor immunity without affecting peripheral T reg cell homeostasis. The p97-Npl4 complex bridges Stat3 with E3 ligases PDLIM2 and PDLIM5, thereby promoting Stat3 degradation and enabling TI-T reg cell development. Collectively, this work shows an important role for the p97-Npl4 complex in controlling T reg -T H 17 cell balance in tumors and identifies possible targets for immunotherapy.
Keyphrases
  • cancer therapy
  • single cell
  • cell therapy
  • cell proliferation
  • cell cycle arrest
  • stem cells
  • gene expression
  • cell death
  • mesenchymal stem cells
  • risk assessment
  • bone marrow
  • pi k akt