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Novel drug-free cascaded nanoparticles induce tumor-specific ROS storms via multimodal synergistic anticancer therapy
Mingsen Wen1, Hongwei Chen2, Song Xu1
1Guangxi Key Laboratory of Special Biomedicine, School of Medicine, Guangxi University, Nanning, 530004, Guangxi, China.
Abstract:
Reactive oxygen species (ROS), generated by sonosensitizers, play a pivotal role in tumor cell apoptosis during sonodynamic therapy (SDT), particularly for tumors located deep within tissues. Nevertheless, conventional sonosensitizers present limitations including inadequate ROS generation, insufficient tumor-specific accumulation, and associated adverse effects, significantly restricting their clinical applicability. To address these limitations, novel drug-free multifunctional nanoparticles (designated HGMP NPs) were synthesized. These NPs consist of mesoporous polydopamine (MPDA)-loaded protoporphyrin IX (PpIX), further surface-modified with glucose oxidase (GOx) and hyaluronic acid (HA), to achieve integrated photothermal, sonodynamic, and starvation-based tumor therapy. Upon exposure to near-infrared (NIR) irradiation (808 nm) combined with ultrasound (US), HGMP NPs exhibited pronounced synergistic anticancer effects. Specifically, the photothermal effect triggered by NIR irradiation effectively enhanced local oxygen supply within tumor sites, thus significantly augmenting ROS production and improving the therapeutic outcomes of SDT. Concurrently, GOx-mediated glucose depletion induced tumor starvation and produced hydrogen peroxide (H2O2), further exacerbating oxidative stress within the tumor microenvironment. Transcriptomic analysis revealed that ROS and TNF signaling pathways represented key mechanisms underlying tumor elimination by this multimodal synergistic strategy. Real-time PCR analysis and ELISA assays further validated activation of the TNF signaling pathway. Importantly, this study first confirmed the high biocompatibility and biosafety of HGMP NPs via serum metabolomics, demonstrating no detectable systemic metabolic perturbations. Collectively, the prepared HGMP NPs provide a rational paradigm for synergistic anticancer therapy. These findings highlight the potential of HGMP NPs as an exceptionally safe and effective nanoplatform for cancer treatment, offering valuable insights into future developments in cancer nanomedicine.
Insights
Novel nanoparticles enhance sonodynamic therapy by increasing oxygen and starving tumors, showing promise for safe and effective cancer treatment.
Area of Science:
- Biomedical Engineering
- Nanomedicine
- Cancer Therapy
Background:
- Sonodynamic therapy (SDT) uses reactive oxygen species (ROS) for tumor apoptosis, but conventional agents have limitations.
- Challenges include poor ROS generation, limited tumor accumulation, and side effects, hindering clinical use.
Purpose of the Study:
- To develop novel, drug-free multifunctional nanoparticles (HGMP NPs) for integrated photothermal, sonodynamic, and starvation therapy.
- To overcome limitations of conventional sonosensitizers for deep-seated tumors.
Main Methods:
- Synthesized mesoporous polydopamine (MPDA)-loaded protoporphyrin IX (PpIX) nanoparticles, surface-modified with glucose oxidase (GOx) and hyaluronic acid (HA).
- Investigated synergistic anticancer effects using near-infrared (NIR) irradiation and ultrasound (US).
- Analyzed tumor elimination mechanisms via transcriptomics, real-time PCR, and ELISA; assessed biosafety using serum metabolomics.
Main Results:
- HGMP NPs combined with NIR and US demonstrated significant synergistic anticancer effects.
- NIR irradiation enhanced local oxygen, boosting ROS production and SDT efficacy.
- GOx-mediated glucose depletion induced tumor starvation and H2O2 production, increasing oxidative stress.
- Transcriptomic analysis identified ROS and TNF signaling pathways as key mechanisms.
- Serum metabolomics confirmed high biocompatibility and biosafety of HGMP NPs without systemic metabolic disruption.
Conclusions:
- The developed HGMP NPs offer a rational platform for synergistic anticancer therapy.
- These nanoparticles show potential as a safe and effective nanoplatform for cancer treatment.
- Findings provide insights for future developments in cancer nanomedicine.
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