DNAzyme-Mediated Cascade Nanoreactor for Cuproptosis-Promoted Pancreatic Cancer Synergistic Therapy.
Qiao YuJie ZhouYong LiuXiao Qiong LiShan LiHong ZhouBin KangHong-Yuan ChenJing-Juan XuPublished in: Advanced healthcare materials (2023)
Cuproptosis, a kind of newly-recognized cell death modality, shows enormous prospect in cancer treatment. The inducer of cuproptosis has more advantages in tumor therapy, especially that could trigger cuproptosis and chemodynamic therapy (CDT) simultaneously. However, cuproptosis is restricted to the deficiency of intracellular copper ions and the non-specific delivery of copper-based ionophores. Therefore, high level delivery, responsive release and utilizing synergistic-function of inducer become the key on cuproptosis-based oncotherapy. In this work, we constructed a cascade nanosystem for enhanced cuproptosis and CDT. In the weak acidic environment of tumor cells, DNA, zinc ions and Cu + could release from the nanosystem. Since Cu + having superior performance in mediating both Fenton-like reaction and cuproptosis, the released Cu + induced cuproptosis and CDT efficiently, accompanied by Cu 2+ generation. Then Cu 2+ could be converted into Cu + partially by glutathione (GSH) to from a Cu + supply loop and ensure the synergistic action. Meanwhile, the consumption of GSH also contributed to cuproptosis and CDT in return. Finally, DNA and Zn 2+ formed DNAzyme to shear catalase-related RNA, resulting in the accumulation of hydrogen peroxide and further enhancing combination therapy. These results provide a promising nano-therapeutic platform and may inspire the design for potential cancer treatment based on cuproptosis. This article is protected by copyright. All rights reserved.
Keyphrases
- replacement therapy
- aqueous solution
- smoking cessation
- hydrogen peroxide
- combination therapy
- cell death
- metal organic framework
- cancer therapy
- wastewater treatment
- nitric oxide
- single molecule
- mesenchymal stem cells
- drug delivery
- living cells
- high throughput
- climate change
- cell therapy
- nucleic acid
- high glucose
- heavy metals
- label free
- current status
- cell cycle arrest