Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy

被引:122
|
作者
Zhan, Qi [1 ]
Yi, Kaikai [2 ]
Qi, Hongzhao [3 ]
Li, Sidi [1 ]
Li, Xueping [1 ]
Wang, Qixue [2 ]
Wang, Yunfei [2 ]
Liu, Chaoyong [2 ]
Qiu, Mingzhe [2 ]
Yuan, Xubo [1 ]
Zhao, Jin [1 ]
Hou, Xin [1 ]
Kang, Chunsheng [2 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin Key Lab Composite & Funct Mat, Tianjin 300072, Peoples R China
[2] Tianjin Med Univ, Key Lab Postneurotrauma Neurorepair & Regenerat C, Minist Educ & Tianjin City,Gen Hosp, Dept Neurosurg,Tianjin Neurol Inst,Lab Neurooncol, Tianjin 300052, Peoples R China
[3] Qingdao Univ, Inst Translat Med, Qingdao 266021, Peoples R China
来源
THERANOSTICS | 2020年 / 10卷 / 17期
基金
中国国家自然科学基金;
关键词
exosome; co-loading; tumor targeting; efficient transfection; combination therapy; EXTRACELLULAR VESICLES; CANCER; DELIVERY; NANOMATERIALS; NANOMEDICINE; MICRORNA-21; BARRIERS; RELEASE; POLYMER; SIRNA;
D O I
10.7150/thno.45028
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Rationale: Developing an effective nanoplatform to realize 'multi-in-one' is essential to broaden the therapeutic potential of combination therapy. Exosomes are ideal candidates since their intrinsic abilities of integrating multiple contents and functions. However, only limited efforts have been devoted to engineering exosomes to integrate the needed properties, also considering the safety and yield, for tumor-targeted and efficient gene/chemo combination therapy. Methods: Herein, by manipulating the exosome membrane, blood exosomes with high abundance and safety are engineered as a versatile combinatorial delivery system, where the doxorubicin (Dox) and cholesterol-modified miRNA21 inhibitor (miR-21i) are co-embedded into the lipid bilayer of exosomes, and the magnetic molecules and endosomolytic peptides L17E are bind to the exosome membrane through ligand-receptor coupling and electrostatic interactions, respectively. Results: It is proved that such engineering strategy not only preserves their intrinsic features, but also readily integrates multiple properties of tumor targeting, efficient transfection and gene/chemo combination therapy into blood exosomes. The lipid bilayer structure of exosomes allows them to co-load Dox and miR-21i with high-payloads. Moreover, profiting from the integration of magnetic molecules and L17E peptides, the engineered exosomes exhibit an enhanced tumor accumulation and an improved endosome escape ability, thereby specifically and efficiently delivering encapsulated cargos to tumor cells. As a result, a remarkable inhibition of tumor growth is observed in the tumor-bearing mice, and without noticeable side effects. Conclusions: This study demonstrates the potential of engineered blood exosomes as feasible co-delivery nanosystem for tumor-targeted and efficient combination therapy. Further development by replacing the drugs combined regimens can potentially make this engineered exosome become a general platform for the design of safe and effective combination therapy modality.
引用
收藏
页码:7889 / 7905
页数:17
相关论文
共 50 条
  • [1] Long circulation and tumor-targeting biomimetic nanoparticles for efficient chemo/photothermal synergistic therapy
    Zhang, Yifan
    Yue, Xuanyu
    Yang, Shengchao
    Li, Xianglong
    Cui, Lin
    Cui, Xiaobin
    Shi, Yue
    Liu, Zhiyong
    Guo, Xuhong
    Li, Yongsheng
    JOURNAL OF MATERIALS CHEMISTRY B, 2022, 10 (26) : 5035 - 5044
  • [2] Designer exosomes enabling tumor targeted efficient chemo/gene/ photothermal therapy
    Wang, Jie
    Chen, Peng
    Dong, Yue
    Xie, Han
    Wang, Yachao
    Soto, Fernando
    Ma, Peng
    Feng, Xiaojun
    Du, Wei
    Liu, Bi-Feng
    BIOMATERIALS, 2021, 276
  • [3] Engineering a HEK-293T exosome-based delivery platform for efficient tumor-targeting chemotherapy/internal irradiation combination therapy
    Congcong Wang
    Ning Li
    Yutian Li
    Shasha Hou
    Wenxin Zhang
    Zhaowei Meng
    Shen Wang
    Qiang Jia
    Jian Tan
    Renfei Wang
    Ruiguo Zhang
    Journal of Nanobiotechnology, 20
  • [4] Engineering a HEK-293T exosome-based delivery platform for efficient tumor-targeting chemotherapy/internal irradiation combination therapy
    Wang, Congcong
    Li, Ning
    Li, Yutian
    Hou, Shasha
    Zhang, Wenxin
    Meng, Zhaowei
    Wang, Shen
    Jia, Qiang
    Tan, Jian
    Wang, Renfei
    Zhang, Ruiguo
    JOURNAL OF NANOBIOTECHNOLOGY, 2022, 20 (01)
  • [5] Glucosylated polyethylenimine as a tumor-targeting gene carrier
    In -Kyu Park
    Seung -Eun Cook
    You -Kyoung Kim
    Hyun -Woo Kim
    Myung -Haing Cho
    Hwan -Jeong Jeong
    Eun -Mi Kim
    Jae -Woon Nah
    Hee -Seung Born
    Chong -Su Cho
    Archives of Pharmacal Research, 2005, 28 : 1302 - 1310
  • [6] Glucosylated polyethylenimine as a tumor-targeting gene carrier
    Park, IK
    Cook, SE
    Kim, YK
    Kim, HW
    Cho, MH
    Jeong, HJ
    Kim, EM
    Nah, JW
    Bom, HS
    Cho, CS
    ARCHIVES OF PHARMACAL RESEARCH, 2005, 28 (11) : 1302 - 1310
  • [7] Tumor-Targeting and Microenvironment-Responsive Smart Nanoparticles for Combination Therapy of Antiangiogenesis and Apoptosis
    Huang, Shixian
    Shao, Kun
    Liu, Yang
    Kuang, Yuyang
    Li, Jianfeng
    An, Sal
    Guo, Yubo
    Ma, Haojun
    Jiang, Chen
    ACS NANO, 2013, 7 (03) : 2860 - 2871
  • [8] CANCER THERAPY Selective Tumor-Targeting with Prodrugs
    Oltmanns, Doerte
    CHEMIE IN UNSERER ZEIT, 2015, 49 (02) : 93 - 93
  • [9] Remodeling of Tumor Microenvironment by Tumor-Targeting Nanozymes Enhances Immune Activation of CAR T Cells for Combination Therapy
    Zhu, Lipeng
    Liu, Jie
    Zhou, Guangyu
    Liu, Tzu-Ming
    Dai, Yunlu
    Nie, Guangjun
    Zhao, Qi
    SMALL, 2021, 17 (43)
  • [10] A tumor-targeting black phosphorus-based nanoplatform for controlled chemo-photothermal therapy of breast cancer
    Yang, Lin
    Zhang, Ying
    Liu, Jing
    Wang, Xiaofen
    Zhang, Li
    Wan, Hao
    MATERIALS TODAY BIO, 2025, 31