Authors
Gang Shu, Chenya Wang, Zhenxing Sun, Jinbin Pan, Cai Zhang, Jiaojiao Yu, Xiang Jing, Yan Zhou, Zhuang Liu, Shao-Kai Sun
Published in
Advanced healthcare materials. Nov 01, 2026. Epub Nov 01, 2026.
Abstract
Synergistic therapeutic nanoplatforms are of considerable interest in tumor therapy, but their translational potential is often limited by complex multicomponent designs and unknown in vivo degradation behavior. Herein, we show a degradable, single-component manganese nanoparticles (Mn NPs) using liquid-phase exfoliation of commercial bulk manganese powder for cancer therapy. In the acidic tumor environment, Mn NPs react with H+ to generate Mn2+ and H2 and raise the local pH. The released Mn2+ drives Fenton-like reactions to produce ROS, while H2 causes mitochondrial damage, which together lead to tumor cell death. In addition, Mn2+ activates cGAS-STING signaling and initiates antitumor immunity. Moreover, Mn NPs inhibit tumor growth in CT26, 4T1, and B16F10 mouse models and show better effects than Mn2+ alone. Transcriptomic analysis further reveals activation of multiple immune-related signaling pathways following Mn NP treatment. In a bilateral tumor model, unilateral injection of Mn NPs triggers a systemic antitumor immune response, leading to effective inhibition of distant, untreated tumor growth. Collectively, this study identifies Mn NPs as a simple, biodegradable, single-component nanoplatform that offers a promising new route for multimodal tumor therapy.
PMID:
42967870
Bibliographic data and abstract were imported from PubMed on 02 Nov 2026.
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