肿瘤微环境
癌症研究
抑制器
转移
化学
免疫系统
癌细胞
癌症
免疫疗法
共价键
渗透(HVAC)
肿瘤细胞
肿瘤进展
免疫检查点
癌症免疫疗法
胶质母细胞瘤
癌症治疗
癌症治疗
PD-L1
癌症干细胞
共价结合
祖细胞
纳米技术
癌症复发
黑色素瘤
炎症
作者
An Song,Qing Wang,Ben Liu,Qi‐Chao Yang,Zi-Yan Hu,Heng-Tao Lei,Xiao-Long Zhang,Fang-Ling Gao,Wu-Yin Wang,Meng-Jie Zhang,Shuo Wang,Tian-Fu Wu,Liang Zhang,Zhi‐Jun Sun
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-02-02
卷期号:26 (5): 1662-1672
被引量:2
标识
DOI:10.1021/acs.nanolett.5c05157
摘要
Chemoresistance remains a major barrier to effective cancer treatment, leading to tumor recurrence and high mortality. Developing strategies to combat chemoresistant tumors is therefore an urgent challenge. Here, we report a covalent organic framework (COF) nanomedicine, 3N-DPQ-COF, designed to target chemoresistant cancers. Mechanistic studies reveal that 3N-DPQ-COF accumulates efficiently in resistant tumor cells and suppresses cancer stemness in 4T1 and CT26 models, outperforming doxorubicin. Moreover, 3N-DPQ-COF promotes CD8 + T-cell infiltration and reduces the number of immunosuppressive erythroid progenitor cells and myeloid-derived suppressor cells, thereby remodeling the tumor microenvironment (TME) and inducing GSDME-dependent pyroptosis. Remarkably, even without checkpoint blockade, 3N-DPQ-COF suppresses metastasis and recurrence in chemoresistant 4T1 tumors, achieving >90% tumor inhibition and cure rates exceeding 80%. This study highlights the potential of AIEgen-based COF nanomedicines for overcoming chemoresistance through concurrent modulation of tumor stemness, pyroptosis, and immune activation.
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