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Single-atom Ca nanozyme induces glioma death through Ca2+-overload-enhanced catalytic tumor nanotherapy, ferroptosis and synergistic remodeling of the immune microenvironment

  • Zhizhong Jin (Co-first Author)
  • , Xinqiao Li (Co-first Author)
  • , Xiaoyu Hou (Co-first Author)
  • , Jinpeng Hu
  • , Yue Zhuo
  • , Jianghua Shi
  • , Tao Xu*
  • , Qi Zhao*
  • , Zhitao Jing*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

2 Downloads (CityUHK Scholars)

Abstract

In recent years, nanozyme-based catalytic therapy for tumors has garnered extensive attention. They combine the properties of nanomaterials and enzymes, precisely mimicking the structure of natural enzymes and exhibiting highly efficient catalytic ability. While nanozymes exert favorable catalytic therapeutic effects in the treatment of most tumors, their application in gliomas is limited by the unique physiological environment and the blood-brain barrier. In this study, a calcium atom nanozyme (CaCN) with peroxidase-like (POD-like) properties was developed. It can induce multiple cell death mechanisms in glioma cells, such as calcium overload and ferroptosis, and synergistically modulate the immune microenvironment. After being functionalized with transferrin (TF) targeting ligands and polyethylene glycol (PEG), it selectively crosses the blood-brain barrier, thereby inhibiting the malignant progression of glioma. © The Author(s) 2025.
Original languageEnglish
Article number716
Number of pages19
JournalJournal of Nanobiotechnology
Volume23
Online published13 Nov 2025
DOIs
Publication statusPublished - 2025

Funding

The research was supported by the National Natural Science Foundation of China (No. 82072794) and National Natural Science Foundation of China (No. 82104838).

Research Keywords

  • Single-atom nanozyme
  • Glioblastoma therapy
  • Ferroptosis
  • Pyroptosis
  • Immune reprogramming

Publisher's Copyright Statement

  • This full text is made available under CC-BY-NC-ND 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/

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