Evidence map›Paper›PMID 40531138›Full record

ReviewNanomedicine (London, England)2025

Cancer therapy with engineered nanozymes: from molecular design to tumour-responsive catalysis.

Austine Ofondu Chinomso Iroegbu, Moipone Linda Teffo, Emmanuel Rotimi Sadiku

Erratum issuedAbstract readReview
In one paragraph

Review in Nanomedicine (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Glucose coated FeO@FeScientific reports · 2026
    Article
  5. Review
  6. Review
  7. Targeted therapy and biomarker-guided applications of ecofriendly silver nanoparticles in precision oncology.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Austine Ofondu Chinomso IroegbuDepartment of Chemical, Metallurgical and Materials Engineering, Institute for Nano-Engineering Research (INER), Tshwane University of Technology, Pretoria, South Africa.ORCID 0000-0001-9235-6554
Moipone Linda TeffoDepartment of Chemical, Metallurgical and Materials Engineering, Institute for Nano-Engineering Research (INER), Tshwane University of Technology, Pretoria, South Africa.ORCID 0000-0003-0347-7034
Emmanuel Rotimi SadikuDepartment of Chemical, Metallurgical and Materials Engineering, Institute for Nano-Engineering Research (INER), Tshwane University of Technology, Pretoria, South Africa.ORCID 0000-0002-8504-1041

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanozymes, engineered nanomaterials that mimic natural enzyme activity, have emerged as powerful tools in precision cancer therapy due to their ability to generate reactive oxygen species (ROS), modulate the tumor microenvironment (TME), and facilitate cascade catalytic reactions. This review presents a comprehensive evaluation of recent innovations in nanozyme structural engineering aimed at improving catalytic performance, substrate specificity, and biocompatibility. Key design strategies, including dimensional tailoring, valence state tuning, and surface functionalisation, are discussed in the context of tumor-targeted therapies. Special focus is given to multifunctional and stimuli-responsive nanozymes that adapt to TME conditions or external triggers like light and pH. Despite significant progress, barriers such as biosafety, delivery efficiency, and lack of standardized catalytic performance metrics remain. This review critically addresses these challenges and highlights state-of-the-art nanozyme platforms, such as single-atom catalysts and cascade systems, which are leading the field toward clinical translation. Finally, it proposes strategic directions to bridge current knowledge gaps and advance nanozymes from bench to bedside, positioning them as next-generation catalytic platforms for personalized oncology.

Indexed as

NanostructuresNeoplasmsAnimalsAntineoplastic AgentsCatalysisHumansReactive Oxygen SpeciesTumor MicroenvironmentAntineoplastic AgentsReactive Oxygen SpeciesanticancercatalaseNanozymesoxidaseperoxidasesuperoxide dismutase

Identifiers

PMID40531138
PMCPMC12239811

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.