A Heterojunction Structured WO2.9-WSe2 Nanoradiosensitizer Increases Local Tumor Ablation and Checkpoint Blockade Immunotherapy upon Low Radiation Dose.
Xinghua DongRan ChengShuang ZhuHuimin LiuRuyi ZhouChenyang ZhangKui ChenLinqiang MeiChengyan WangChunjian SuXiangfeng LiuZhanjun GuYuliang ZhaoPublished in: ACS nano (2020)
Radiotherapy (RT) in practical use often suffers from off-target side effects and ineffectiveness against hypoxic tumor microenvironment (TME) as well as remote metastases. With regard to these problems, herein, we provide semiconductor heterojunction structured WO2.9-WSe2-PEG nanoparticles to realize a synergistic RT/photothermal therapy (PTT)/checkpoint blockade immunotherapy (CBT) for enhanced antitumor and antimetastatic effect. Based on the heterojunction structured nanoparticle with high Z element, the nanosystem could realize non-oxygen-dependent reactive oxygen species generation by catalyzing highly expressed H2O2 in TME upon X-ray irradiation, which could further induce immunogenic cell death. Meanwhile, this nanosystem could also induce hyperthermia upon near-infrared irradiation to enhance RT outcome. With the addition of anti-PD-L1 antibody-based CBT, our results give potent evidence that local RT/PTT upon mild temperature and low radiation dose could efficiently ablate local tumors and inhibit tumor metastasis as well as prevent tumor rechallenge. Our study provides not only one kind of radiosensitizer based on semiconductor nanoparticles but also a versatile nanoplatform for simultaneous triple-combined therapy (RT/PTT/CBT) for treating both local and metastasis tumors.
Keyphrases
- cell death
- visible light
- reactive oxygen species
- dna damage
- cell cycle
- solar cells
- mental health
- early stage
- radiation induced
- room temperature
- radiation therapy
- high resolution
- magnetic resonance imaging
- perovskite solar cells
- stem cells
- magnetic resonance
- bone marrow
- oxidative stress
- atrial fibrillation
- signaling pathway
- electron microscopy