Tetrahedron DNA nanostructure/iron-based nanomaterials for combined tumor therapy

被引:2
|
作者
Xu, Jiangshan [1 ,2 ]
Zhang, Weifei [3 ]
Cai, Zhengwen [2 ]
Li, Yong [4 ]
Bai, Long [4 ]
Gao, Shaojingya [2 ]
Sun, Qiang [2 ,5 ]
Lin, Yunfeng [1 ,2 ,5 ]
机构
[1] Sichuan Univ, Coll Biomed Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, West China Hosp Stomatol, Natl Clin Res Ctr Oral Dis, State Key Lab Oral Dis,Natl Ctr Stomatol, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, Orthoped Res Inst, Dept Orthoped, Chengdu 610041, Peoples R China
[4] Southwest Med Univ, Affiliated Stomatol Hosp, Dept Oral Implantol, Luzhou 646000, Peoples R China
[5] Sichuan Prov Engn Res Ctr Oral Biomat, Chengdu 610041, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Tetrahedron DNA nanostructure; Ferroptosis; Doxorubicin; Breast cancer; Combined cancer therapy; TRANSFERRIN RECEPTOR; TARGETED THERAPY; CELL-DEATH; FERROPTOSIS; CANCER; DOXORUBICIN;
D O I
10.1016/j.cclet.2024.109620
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Triple-negative breast cancer, due to its aggressive nature and lack of targeted treatment, faces serious challenges in breast cancer treatment. Conventional therapies, such as chemotherapy, are encumbered by a range of limitations, and there is an urgent need for more effective treatment strategies. Ferroptosis, as an iron-dependent form of cell death, has exhibited promising potential in cancer treatment. Combining ferroptosis with other cancer therapies offers new avenues for treatment. Tetrahedral DNA nanostructure (TDN), a novel DNA-based three-dimensional (3D) nanomaterial, is promising drug delivery vehicle and can be utilized for functionalizing inorganic nanomaterials. In this work, we have demonstrated the preparation of Fe3 O4 -PEI@TDN-DOX nanocomposites and elucidated their antitumor mechanism. The TDN facilitated the enhanced cellular uptake of polyetherimide (PEI)-modified Fe3 O4 , and the delivery of the chemotherapeutic drug doxorubicin (DOX) further augmented their anti-tumor effect. This novel strategy can destroy the tumor redox homeostasis and produce overwhelming lipid peroxides, consequently sensitizing the tumor to ferroptosis. The integration of ferroptosis with other cancer therapies opens up new possibilities for treatment. This research provides valuable mechanistic insights and practical strategies for leveraging nanotechnology to induce ferroptosis and amplify its impact on tumor cells. (c) 2024 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页数:7
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