Advanced Materials · 2017 · 174 citations · 28 references
MedicineOncologyPharmacologyApoptosisChemotherapyMolecular OncologyApoptosis In CancerCancer MetabolismCancer NanomedicineMalignant NeoplasmsMitochondrial Redox BiologyReactive Oxygen SpeciesCancer NanotherapyChemotherapy-induced ApoptosisMitochondrial Biogenesis In CancerOxidative Stress In CancerOxidative Stress InjuryPhotocatalytic NanomaterialsPhotocatalytic OxidationRedox Metabolism In Cancer
Abstract Continuous exposure to carbon monoxide (CO) can sensitize cancer cells to chemotherapy while protect normal cells from apoptosis. The Janus face of CO thus provides an ideal strategy for cancer therapy. Here, a photocatalytic nanomaterial (HisAgCCN) is introduced to transform endogenous CO 2 to CO for improving cancer therapy in vivo. The CO production rate of HisAgCCN reaches to 65 µmol h −1 g mat −1 , which can significantly increase the cytotoxicity of anticancer drug (doxorubicin, DOX) by 70%. Interestingly, this study finds that HisAgCCN can enhance mitochondria biogenesis and aggravate oxidative stress in cancer cells, whereas protect normal cells from chemotherapy‐induced apoptosis as well. Proteomics and metabolomics studies reveal that HisAgCCN can enhance mitochondria biogenesis and aggravate oxidative stress in cancer cells specifically. In vivo studies indicate that HisAgCCN/DOX combination therapy presents a synergetic tumor inhibition, which might provide a new direction for clinical cancer therapy.
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