Angewandte Chemie International Edition · 2019 · 211 citations · 16 references
PharmacyCancer BiologyOncologyChemotherapyNanomaterialsTheranosticsCancer NanomedicineHypoxia AdaptationInorganic NanoparticlesNanomedicineNanoparticle DesignTheranostic NanoparticlesAnticancer ActivityAnticancer ChemotherapyCancer NanotherapyHypoxiaHypoxia-driven Therapy ResistanceHypoxia-mediated ResistanceSystemic Therapy ToxicityTumor Microenvironment Hypoxia
Abstract Tumor hypoxia, the “Achilles’ heel” of current cancer therapies, is indispensable to drug resistance and poor therapeutic outcomes especially for radiotherapy. Here we propose an in situ catalytic oxygenation strategy in tumor using porphyrinic metal‐organic framework (MOF)‐gold nanoparticles (AuNPs) nanohybrid as a therapeutic platform to achieve O 2 ‐evolving chemoradiotherapy. The AuNPs decorated on the surface of MOF effectively stabilize the nanocomposite and serve as radiosensitizers, whereas the MOF scaffold acts as a container to encapsulate chemotherapeutic drug doxorubicin. In vitro and in vivo studies verify that the catalase‐like nanohybrid significantly enhances the radiotherapy effect, alleviating tumor hypoxia and achieving synergistic anticancer efficacy. This hybrid nanomaterial remarkably suppresses the tumor growth with minimized systemic toxicity, opening new horizons for the next generation of theranostic nanomedicines.
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Production of large amounts of hydrogen peroxide by human tumor cells.
Ted P. Szatrowski, Carl Nathan · PubMed · 1991 · 2.5K citations
Qian Chen, Liangzhu Feng, Jingjing Liu et al. · Advanced Materials · 2016 · 1K citations
Pharmacy, Oncology, Pharmaceutics +17
Chunbai He, Kuangda Lu, Demin Liu et al. · Journal of the American Chemical Society · 2014 · 869 citations · Full text
Pharmacy, Oncology, Pharmacology +17