ArticleMaterials today. Bio2026
Spermine oxidase-DOX conjugates reshape tumor microenvironment via carbonyl stress to potentiate bladder cancer chemotherapy.
Article in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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.
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15 authors.
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Abstract
The tumor's antioxidant defenses restrict the efficacy of standard therapies, resulting in compromised treatment responses and systemic tolerance. Conventional redox-disrupting strategies, designed to generate reactive oxygen species (ROS), are limited by both their reliance on single generation methods and the rapid clearance. Herein, we report an innovative strategy that employs spermine oxidase (SMOX) to catalyze the production of endogenous and highly cytotoxic acrolein, thereby creating a destructive carbonyl stress microenvironment to potentiate antineoplastic drug's efficacy. As an example, SMOX and doxorubicin (DOX) were conjugated and co-encapsulated within mesoporous silica nanoparticles to form an integrated delivery platform (PMD). Notably,
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