TY - JOUR
T1 - A polymeric triple-enzyme nanoparticle by light activatable crosslinking for cascade catalytic therapy of osteosarcoma
AU - Ren, Lanfang
AU - Yu, Xin
AU - Yuan, Chunyang
AU - Zhu, Fang
AU - Zhou, Haohan
AU - Chen, Qianqian
AU - Lv, Jia
AU - Mei, Zhoufang
AU - Cheng, Yiyun
AU - Sun, Zhengwang
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2026/3
Y1 - 2026/3
N2 - Multi-enzymatic cascade reactions play fundamental roles in biosynthesis, energetic metabolism, cell signaling, proliferation and apoptosis in living cells. Such reactions have been proposed for cancer therapy via overproducing reactive oxygen species, depleting nutrients for tumor starvation, or remodeling immunosuppressive microenvironment, however, co-delivery of multiple enzymes with optimal cascade catalytic activity remains challenging. Here, we propose a polymer nanoparticle loaded with glucose oxidase (GOx), lactate oxidase (LOx), and chloroperoxidase (CPO) for synergistic cancer catalytic therapy. The enzymes were complexed with O-nitrobenzyl-modified ε-polylysine via ionic and hydrophobic interactions, followed by light-activated crosslinking to prepare serum-stable and pH-responsive protein nanoparticles. The GOx and LOx in the nanoparticle efficiently deplete glucose and lactate, generating excessive hydrogen peroxide, while CPO further catalyze hydrogen peroxide in the presence of chloride ions to produce singlet oxygen (1O2), promoting both apoptosis and ferroptosis in cancer cells. The triple-enzyme polymer nanoparticles efficiently inhibit tumor growth in an osteosarcoma model without causing obvious adverse effects. This multi-enzyme delivery system provides a promising tool for the treatment of diseases via multi-enzymatic cascade reactions.
AB - Multi-enzymatic cascade reactions play fundamental roles in biosynthesis, energetic metabolism, cell signaling, proliferation and apoptosis in living cells. Such reactions have been proposed for cancer therapy via overproducing reactive oxygen species, depleting nutrients for tumor starvation, or remodeling immunosuppressive microenvironment, however, co-delivery of multiple enzymes with optimal cascade catalytic activity remains challenging. Here, we propose a polymer nanoparticle loaded with glucose oxidase (GOx), lactate oxidase (LOx), and chloroperoxidase (CPO) for synergistic cancer catalytic therapy. The enzymes were complexed with O-nitrobenzyl-modified ε-polylysine via ionic and hydrophobic interactions, followed by light-activated crosslinking to prepare serum-stable and pH-responsive protein nanoparticles. The GOx and LOx in the nanoparticle efficiently deplete glucose and lactate, generating excessive hydrogen peroxide, while CPO further catalyze hydrogen peroxide in the presence of chloride ions to produce singlet oxygen (1O2), promoting both apoptosis and ferroptosis in cancer cells. The triple-enzyme polymer nanoparticles efficiently inhibit tumor growth in an osteosarcoma model without causing obvious adverse effects. This multi-enzyme delivery system provides a promising tool for the treatment of diseases via multi-enzymatic cascade reactions.
KW - Cascade enzyme reactions
KW - Catalytic cancer therapy
KW - Intracellular protein delivery
KW - Polymer
KW - Protein nanoparticles
UR - https://www.scopus.com/pages/publications/105020915505
U2 - 10.1016/j.bioactmat.2025.10.042
DO - 10.1016/j.bioactmat.2025.10.042
M3 - 文章
AN - SCOPUS:105020915505
SN - 2452-199X
VL - 57
SP - 93
EP - 104
JO - Bioactive Materials
JF - Bioactive Materials
ER -