H<sub>2</sub>O<sub>2</sub>‐Generating Advanced Nanomaterials for Cancer Treatment

Abstract Tumor cells exploit abnormal redox homeostasis and the pro‐tumorigenic effect of reactive oxygen species (ROS) to enhance their survival and progression. However, excessively high levels of ROS can exceed the oxidative stress threshold of tumor cells, inducing cell death. This can occur by selectively elevating the concentration of H 2 O 2 in tumor cells through both endogenous and exogenous mechanisms. The generated H 2 O 2 serves as a precursor for toxic ROS, such as • OH and 1 O 2 , via chemodynamic and photodynamic therapy, respectively, leading to apoptosis, necrosis, and ferroptosis. Strategies to boost H 2 O 2 levels include direct delivery of exogenous H 2 O 2 and amplifying endogenous H 2 O 2 generation by inhibiting antioxidant enzymes, leveraging glucose oxidase, employing photocatalytic therapy (PCT), and utilizing metal peroxides. Among them, metal peroxides have displayed remarkable performance due to their excellent potential to elevate H 2 O 2 concentration within tumor cells while simultaneously normalizing the acidic and hypoxic conditions of the tumor microenvironment (TME). Moreover, these nanostructures enhance tumor sensitivity to complementary treatments, like chemotherapy. This review summarizes advanced perspectives in the design, synthesis, and comparative analysis of H 2 O 2 ‐generating nanoplatforms, emphasizing their capacity to treat various cancers.

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Publication Details

Journal
Advanced Functional Materials
Published
2025-02-21
DOI
https://doi.org/10.1002/adfm.202425866
Citations
36
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
24.27
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article

H2O2‐Generating Advanced Nanomaterials for Cancer Treatment

Vahideh Nosrati‐Siahmazgi, Bo Xiao, Kamal Dua, Samin Abbaszadeh et al.
36 citations
Advanced Functional Materials
Nanoplatforms for cancer theranostics
24.27
article

H2O2‐Generating Advanced Nanomaterials for Cancer Treatment

Vahideh Nosrati‐Siahmazgi, Bo Xiao, Kamal Dua, Samin Abbaszadeh, Mohammad‐Ali Shahbazi, Hélder A. Santos, Kiyan Musaie, Saman Rezaei, Kik Marais
article en
36 citations

Abstract

Abstract Tumor cells exploit abnormal redox homeostasis and the pro‐tumorigenic effect of reactive oxygen species (ROS) to enhance their survival and progression. However, excessively high levels of ROS can exceed the oxidative stress threshold of tumor cells, inducing cell death. This can occur by selectively elevating the concentration of H 2 O 2 in tumor cells through both endogenous and exogenous mechanisms. The generated H 2 O 2 serves as a precursor for toxic ROS, such as • OH and 1 O 2 , via chemodynamic and photodynamic therapy, respectively, leading to apoptosis, necrosis, and ferroptosis. Strategies to boost H 2 O 2 levels include direct delivery of exogenous H 2 O 2 and amplifying endogenous H 2 O 2 generation by inhibiting antioxidant enzymes, leveraging glucose oxidase, employing photocatalytic therapy (PCT), and utilizing metal peroxides. Among them, metal peroxides have displayed remarkable performance due to their excellent potential to elevate H 2 O 2 concentration within tumor cells while simultaneously normalizing the acidic and hypoxic conditions of the tumor microenvironment (TME). Moreover, these nanostructures enhance tumor sensitivity to complementary treatments, like chemotherapy. This review summarizes advanced perspectives in the design, synthesis, and comparative analysis of H 2 O 2 ‐generating nanoplatforms, emphasizing their capacity to treat various cancers.

Advanced Functional MaterialsVol. 35(28)
University of Technology Sydney (AU), Zanjan University of Medical Sciences (IR), University Medical Center Groningen (NL), University of Electronic Science and Technology of China (CN), University of Groningen (NL), Urmia University (IR), Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital (CN), Urmia University of Medical Sciences (IR)
Openalex Percentile: Top 0%
Nanoplatforms for cancer theranostics
24.27
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