Light-inducible nanodrug-mediated photodynamic and anti-apoptotic synergy for enhanced immunotherapy in triple-negative breast cancer

被引:3
作者
Huang, Jing [1 ,2 ,3 ]
Liu, Xingliang [1 ,2 ,3 ]
Lin, Minzhao [2 ]
Xiao, Zecong [1 ]
Shuai, Xintao [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 3, Nanomed Res Ctr, Guangzhou 510630, Peoples R China
[2] Sun Yat Sen Univ, Sch Mat Sci & Engn, PCFM Lab, Minist Educ, Guangzhou 510275, Peoples R China
[3] Westlake Univ, Sch Engn, Hangzhou 310030, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
CHEMOTHERAPY; BCL-2; CELLS;
D O I
10.1039/d4bm00083h
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Triple negative breast cancer (TNBC) exhibits limited responsiveness to immunotherapy owing to its immunosuppressive tumor microenvironment (TME). Here, a reactive oxygen species (ROS)-labile nanodrug encapsulating the photosensitizer Ce6 and Bcl-2 inhibitor ABT-737 was developed to provoke a robust immune response via the synergistic effect of photodynamic therapy (PDT) and the reversal of apoptosis resistance. Upon exposure to first-wave near-infrared laser irradiation, the generated ROS triggers PEG cleavage, facilitating the accumulation of the nanodrug at tumor region and endocytosis by tumor cells. Further irradiation leads to the substantial generation of cytotoxic ROS, initiating an immunogenic cell death (ICD) cascade, which prompts the maturation of dendritic cells (DCs) as well as the infiltration of T cells into the tumor site. Meanwhile, Bcl-2 inhibition counteracts apoptosis resistance, thereby amplifying PDT-induced ICD and bolstering antitumor immunity. As a result, the ROS-sensitive nanodrug demonstrates a potent inhibitory effect on tumor growth.
引用
收藏
页码:2639 / 2647
页数:9
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