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Efficacy and Mechanism of a Biomimetic Nanosystem Carrying Doxorubicin and an IDO Inhibitor for Treatment of Advanced Triple-Negative Breast Cancer.
Hu, Chuling; Liu, Yan; Cao, Wei; Li, Na; Gao, Shen; Wang, Zhuo; Gu, Fenfen.
  • Hu C; Department of Pharmacy, Jiaxing Maternity and Child Health Care Hospital, Affiliated Women and Children's Hospital of Jiaxing University, Jiaxing, People's Republic of China.
  • Liu Y; Department of Clinical Pharmacy, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
  • Cao W; Department of Neurovascular Disease, Shanghai Fourth People's Hospital, School of Medicine, Tongji University, Shanghai, People's Republic of China.
  • Li N; Department of Pathology, Jiaxing Maternity and Child Health Care Hospital, Affiliated Women and Children's Hospital of Jiaxing University, Jiaxing, People's Republic of China.
  • Gao S; Department of Pharmacy, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
  • Wang Z; Department of Pharmacy, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
  • Gu F; Department of Clinical Pharmacy, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
Int J Nanomedicine ; 19: 507-526, 2024.
Article en En | MEDLINE | ID: mdl-38260240
ABSTRACT

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 1.56-fold 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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dioxigenasas / Inhibidores Enzimáticos / Neoplasias de la Mama Triple Negativas Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dioxigenasas / Inhibidores Enzimáticos / Neoplasias de la Mama Triple Negativas Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article