Sorafenib delivered by cancer cell membrane remodels tumor microenvironment to enhances the immunotherapy of mitoxantrone in breast cancer

被引:1
作者
Chen, Jing [1 ,2 ]
Huang, Jian [1 ,3 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Breast Surg, Hangzhou 310009, Zhejiang, Peoples R China
[2] Univ Chinese Acad Sci, Zhejiang Canc Hosp, Canc Hosp, Dept Radiat Oncol, Hangzhou 310022, Zhejiang, Peoples R China
[3] Key Lab Tumor Microenvironm & Immune Therapy Zhej, Hangzhou 310009, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
biomedical; biomaterial; biomimetic (assembly); PHOTOTHERMAL THERAPY; NANOPARTICLES; CHEMOTHERAPY; DOXORUBICIN; HYPOXIA; SYSTEMS; DNA;
D O I
10.1557/jmr.2020.321
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The negative regulation effect of tumor microenvironment (TME) greatly compromised the efficacy of various cancer treatments, especially cancer immunotherapy. As a result, it is generally recognized that remodeling of TME along with the treatment is a promising way to realize satisfactory cancer therapy. Here, in our study, a drug delivery system (DDS) composed cancer cell membrane (CCM) vehicle loaded mitoxantrone (Mit) and sorafenib (Sfn) was proposed with the aim to combine TME regulation and chemotherapy-induced immunotherapy in one platform. Our results confirmed that after treating with this DDS, the Mit induced immunogenic cell death (ICD) could be augmented by Sfn-based TME regulation to realize effective cancer immunotherapy. The Sfn was shown to downregulate of the regulatory T cells (Treg) level while activating the effector T cells of TME. The synergetic TME regulation along with cancer immunotherapy might be a promising way for advanced cancer treatment.
引用
收藏
页码:3296 / 3303
页数:8
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