Chemoimmunological Cascade Cancer Therapy Using Fluorine Assembly Nanomedicine.
Qingyan ZhangPengkai WuJicheng WuHao ShouXinliang MingShuqi WangBeng WangPublished in: ACS nano (2023)
Classical chemotherapeutic drugs may cause immunogenic cell death (ICD), followed by activating CD8 + T cells to promote cell-mediated antitumor immune responses. However, CD8 + T cells become exhausted due to tumor antigens' continuous stimulation, creating a major obstacle to effectively suppressing tumor growth and metastasis. Here, we develop an approach of chemo-gene combinational nanomedicine to bridge and reprogram chemotherapy and immunotherapy. The dually loaded nanomedicine induces ICD in tumor cells through doxorubicin and reverses the antitumor effects of exhausted CD8 + T cells through the small interfering RNA. The synergistic chemo-gene and fluorine assembly nanomedicine enriched in reactive oxygen species and acid-sensitive bonds results in enhanced cancer immunotherapy to inhibit tumor growth and the lung metastasis of breast cancer in a mouse model of breast cancer and melanoma. This study provides an efficient strategy and insights into chemoimmunological cascade therapy for combating malignant metastatic tumors.
Keyphrases
- cancer therapy
- drug delivery
- cell death
- reactive oxygen species
- mouse model
- immune response
- positron emission tomography
- signaling pathway
- copy number
- genome wide
- small cell lung cancer
- pet imaging
- dendritic cells
- genome wide identification
- single cell
- stem cells
- computed tomography
- dna methylation
- gene expression
- mesenchymal stem cells
- cell proliferation
- cell therapy
- cell cycle arrest
- radiation therapy
- toll like receptor
- skin cancer