Metal-organic framework-based photodynamic combined immunotherapy against the distant development of triple-negative breast cancer

被引:8
作者
Liang, Xiaoyan [1 ,2 ]
Mu, Min [1 ,2 ]
Chen, Bo [1 ,2 ]
Fan, Rangrang [3 ]
Chen, Haifeng [3 ]
Zou, Bingwen [1 ,2 ]
Han, Bo [4 ,5 ]
Guo, Gang [1 ,2 ]
机构
[1] Sichuan Univ, Canc Ctr, Dept Biotherapy, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Neurosurg, Chengdu 610041, Peoples R China
[4] Shihezi Univ, Sch Pharm, Shihezi 832003, Peoples R China
[5] Shihezi Univ, Key Lab Xinjiang Phytomed Resource & Utilizat, Minist Educ, Shihezi 832002, Peoples R China
关键词
Triple-negative breast cancer; Metal-organic frameworks; Immunogenic cell death; Photodynamic therapy; Immunotherapy; METABOLISM;
D O I
10.1186/s40824-023-00447-x
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
BackgroundTriple-negative breast cancer (TNBC) is an aggressive, metastatic and apparently drug-resistant subtype of breast cancer with a higher immune response compared to other types of breast cancer. Photodynamic therapy (PDT) has been gaining popularity for its non-invasive nature, minimal side effects, and spatiotemporally controlled benifits. The use of metal-organic frameworks (MOFs) loaded with programmed death-ligand 1 inhibitors (iPD-L1) offers the possibility of combining PDT with immunotherapy.MethodHere, we construct PCN-224, a MOFs with good biocompatibility and biodegradability for the delivery of the PD-L1 small molecule inhibitor BMS-202 to achieve a synergistic anti-tumor strategy of PDT and immunotherapy. Hyaluronic acid (HA) modified PEG (HA-PEG) was synthesized for the outer layer modification of the nanocomplex, which prolongs its systemic circulation time.ResultsIn vitro cellular experiments show that the nanocomplexes irradiated by 660 nm laser has a strong ability to produce singlet oxygen, which effectively induce PDT. PDT with strong immunogenicity leads to tumor necrosis and apoptosis, and induces immunogenic cell death, which causes tumor cells to release danger associated molecular patterns. In combination with iPD-L1, the combination therapy stimulates dendritic cell maturation, promotes T-cell activation and intratumoral infiltration, and reshapes the tumor immune microenvironment to achieve tumor growth inhibition and anti-distant tumor progression.ConclusionsMOFs-based nano-systems as a platform for combination therapy offer a potentially effective strategy for the treatment of TNBC with high metastatic rates.
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页数:18
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