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Nuclear translocation of ISG15 regulated by PPP2R2B inhibits cisplatin resistance of bladder cancer.

Gaowei HuangJinwen LiuAnze YuChenggong LuoJiangquan ZhuYinghan WangZiran DaiLizhen ZhangZihao FengJun LuZhong DongJunhang LuoWei ChenZhen-Hua Chen
Published in: Cellular and molecular life sciences : CMLS (2024)
Cisplatin resistance is a major challenge for systemic therapy against advanced bladder cancer (BC). Little information is available on the regulation of cisplatin resistance and the underlying mechanisms require elucidation. Here, we detected that downregulation of the tumor suppressor, PPP2R2B (a serine/threonine protein phosphatase 2 A regulatory subunit), in BC promoted cell proliferation and migration. What's more, low PPP2R2B expression was correlated with cisplatin resistance. In vitro and in vivo experiments verified that PPP2R2B could promote BC sensitivity to cisplatin. In terms of mechanism, we identified a novel function of PPP2R2B as a nucleocytoplasmic transport molecule. PPP2R2B promoted ISG15 entry into the nucleus by mediating binding of IPO5 with ISG15. Nuclear translocation of ISG15 inhibited DNA repair, further increasing ISG15 expression through activation of the STING pathway. Besides, PPP2R2B was down-regulated by SUV39H1-mediated histone 3 lysine 9 trimethylation, which could be restored by the SUV39H1-specific inhibitor, chaetocin. Our data suggest that PPP2R2B expression level is a potential biomarker for chemotherapy response and that chemotherapy in combination with chaetocin may be a feasible treatment strategy for patients with BC.
Keyphrases
  • poor prognosis
  • dna repair
  • binding protein
  • protein kinase
  • dna damage
  • stem cells
  • dna methylation
  • squamous cell carcinoma
  • transcription factor
  • locally advanced
  • cell therapy
  • mesenchymal stem cells
  • health information