Maximizing arsenic trioxide's anticancer potential: Targeted nanocarriers for solid tumor therapy

被引:2
作者
Yang, Shiqi [1 ]
Raza, Faisal [1 ]
Li, Kunwei [1 ]
Qiu, Yujiao [2 ,3 ]
Su, Jing [1 ]
Qiu, Mingfeng [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200240, Peoples R China
[2] Univ Penn, Wharton Sch, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Nursing, Philadelphia, PA 19104 USA
基金
中国国家自然科学基金;
关键词
Arsenic trioxide; Nanocarriers; Targeted drug delivery; Anticancer mechanisms; Combination therapy; ACUTE PROMYELOCYTIC LEUKEMIA; CANCER STEM-CELLS; LUNG-CANCER; RETINOIC ACID; SILICA NANOPARTICLES; DELIVERY SYSTEM; UP-REGULATION; HIGH-RISK; IN-VITRO; DRUG;
D O I
10.1016/j.colsurfb.2024.114014
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Arsenic trioxide (ATO) has gained significant attention due to its promising therapeutic effects in treating different diseases, particularly acute promyelocytic leukemia (APL). Its potent anticancer mechanisms have been extensively studied. Despite the great efficacy ATO shows in fighting cancers, drawbacks in the clinical use are obvious, especially for solid tumors, which include rapid renal clearance and short half-life, severe adverse effects, and high toxicity to normal cells. Recently, the emergence of nanomedicine offers a potential solution to these limitations. The enhanced biocompatibility, excellent targeting capability, and desirable effectiveness have attracted much interest. Therefore, we summarized various nanocarriers for targeted delivery of ATO to solid tumors. We also provided detailed anticancer mechanisms of ATO in treating cancers, its clinical trials and shortcomings as well as the combination therapy of ATO and other chemotherapeutic agents for reduced drug resistance and synergistic effects. Finally, the future study direction and prospects were also presented.
引用
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页数:16
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