Efficacy and Mechanism of a Biomimetic Nanosystem Carrying Doxorubicin and an IDO Inhibitor for Treatment of Advanced Triple-Negative Breast Cancer

被引:3
|
作者
Hu, Chuling [1 ]
Liu, Yan [2 ]
Cao, Wei [3 ]
Li, Na [4 ]
Gao, Shen [5 ]
Wang, Zhuo [5 ]
Gu, Fenfen [2 ]
机构
[1] Jiaxing Univ, Affiliated Women & Childrens Hosp, Jiaxing Matern & Child Hlth Care Hosp, Dept Pharm, Jiaxing, Peoples R China
[2] Shanghai Jiao Tong Univ, Xinhua Hosp, Sch Med, Dept Clin Pharm, Shanghai, Peoples R China
[3] Tongji Univ, Shanghai Peoples Hosp 4, Sch Med, Dept Neurovasc Dis, Shanghai, Peoples R China
[4] Jiaxing Univ, Jiaxing Matern & Child Hlth Care Hosp, Dept Pathol, Affiliated Women & Childrens Hosp, Jiaxing, Peoples R China
[5] Second Mil Med Univ, Changhai Hosp, Dept Pharm, Shanghai, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2024年 / 19卷
关键词
immunogenic cell death; doxorubicin; bionic nanoparticle; IDO1; inhibitor; triple-negative breast cancer; IMMUNOGENIC CELL-DEATH; IMMUNOTHERAPY; NANOPARTICLES; CHECKPOINT; TUMOR;
D O I
10.2147/IJN.S440332
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Introduction: Chemotherapy is still the treatment of choice for advanced triple-negative breast cancer. Chemotherapy combined with immunotherapy is being tried in patients with triple-negative breast cancer. As a kind of "cold tumor", triple-negative breast cancer has a bottleneck in immunotherapy. Indoleamine 2, 3-dioxygenase-1 inhibitors can reverse the immunosuppressive state and enhance the immune response.Methods: In this study, mesoporous silica nanoparticles were coated with the chemotherapeutic drug doxorubicin and indoleamine 2, 3-dioxygenase 1 inhibitor 1-Methyl-DL-tryptophan (1-MT), and then encapsulate the surfaces of a triple-negative breast cancer cell membrane to construct the tumor dual-targeted delivery system CDIMSN for chemotherapy and immunotherapy, and to investigate the immunogenic death effect of CDIMSN.Results and discussion: The CDIMSN could target the tumor microenvironment. Doxorubicin induced tumor immunogenic death, while 1-MT reversed immunosuppression. In vivo findings showed that the tumor size in the CDIMSN group was 2.66-fold and 1.56fold smaller than that in DOX and DIMSN groups, respectively. CDIMSN group was better than naked DIMSN in stimulating CD8+T cells, CD4+T cells and promoting Dendritic Cells(DC) maturation. In addition, blood analysis, biochemical analysis and Hematoxylin staining analysis of mice showed that the bionic nanoparticles had good biological safety.
引用
收藏
页码:507 / 526
页数:20
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