A CaCO3-based nanoplatform with sonodynamic and tumor microenvironment activated for combined in vitro cancer therapy

被引:2
|
作者
Cai, Jiale [1 ]
Hu, Guiping [1 ]
Hu, Lihua [2 ]
Chen, Junge [1 ]
Chen, Dan [1 ]
Liu, Dan [1 ]
Wang, Xiaolei [1 ]
Hu, Boxian [1 ]
Li, Cheng [1 ]
机构
[1] Beihang Univ, Beijing Adv Innovat Ctr Biomed Engn, Beijing Adv Innovat Ctr Big Data Based Precis Med, Sch Engn Med Beijing, Beijing 100191, Peoples R China
[2] Peking Univ First Hosp, Dept Cardiol, Beijing 100034, Peoples R China
来源
TRANSLATIONAL ONCOLOGY | 2023年 / 38卷
基金
中国国家自然科学基金;
关键词
Sonodynamic therapy; Nitric oxide; CaCO3; Tumor microenvironment; RNA-seq; NITRIC-OXIDE; PHOTODYNAMIC THERAPY; DRUG-DELIVERY; NANOPARTICLES; RESPIRATION; HEALTH; PH;
D O I
10.1016/j.tranon.2023.101771
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Sonodynamic therapy (SDT) has potential clinical applications for cancer therapy, and is yet restricted by complex tumor microenvironmental (TME) factors. Thus, the research problem of TME modulation as well as efficient tumor treatment still needs to be clarified. Method: In this study, a calcium carbonate (CaCO3) nanoplatform was designed for ultrasound (US) and TME response-triggered, which encapsulated Ag2S and loaded with L-Arg, and further wrapped with RBC/Platelet membrane, named as QD@Ca/ML-Arg. Results: Non-invasive US-triggered SDT by Ag2S and acidic environment-responsive drug release were achieved. In vitro experiments validated the efficacy of SDT, Ca-ion interference and nitric oxide (NO) gas therapy as combined therapy for cancer treatment. By means of RNA sequencing, the cancer therapeutic mechanism of SDT in redox-related pathways was elucidated. The immunosuppressive TME was simulated with a M2-macrophage/ cancer cell co-culture system to confirm the immune activating effect of immunogenic cell death (ICD). Conclusion: Accordingly, the potential of QD@Ca/ML-Arg-was demonstrated for in vitro TME modulation, cancer therapeutic efficacy and clinical translation.
引用
收藏
页数:12
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