三阴性乳腺癌
材料科学
寡核苷酸
纳米器件
四面体
化学免疫疗法
癌症研究
DNA
乳腺癌
CpG站点
癌症
纳米技术
结晶学
医学
生物
免疫疗法
遗传学
内科学
基因
DNA甲基化
化学
基因表达
作者
Qipeng Long,Lin Yang,Jiaqi Zhang,Hengchang Zang,Yan Lü,Yu-Fei Wang,Shulong Jiang
标识
DOI:10.1021/acsami.5c07915
摘要
DNA tetrahedron (DT) nanostructures have shown broad application prospects in disease diagnosis and treatment due to their structural programmability, nontoxicity, and efficient cellular uptake. Recently, their potential as ideal nanocarriers for synergistic anticancer drug delivery has been increasingly recognized. In this study, the first use of a DT nanostructure to co-deliver shikonin (SK) and CpG oligonucleotide to achieve chemoimmunotherapy of triple-negative breast cancer (TNBC) is reported. In this nanoplatform, SK serves as both a cytotoxic agent and an immunogenic cell death (ICD) inducer, while CpG-modified DT (CpG-DT) has dual functions of drug carrier and immune adjuvant, which can significantly enhance the ICD effect. CpG-DT/SK exhibits an enhanced water solubility and tumor-specific accumulation. The synergistic combination of SK and CpG further facilitated the maturation of dendritic cells and the subsequent infiltration of CD8+ and CD4+ T cells, thereby achieving effective inhibition of 4T1 tumor growth. This DT-based co-delivery nanoplatform provides a promising strategy for TNBC treatment with great potential for clinical translation.
科研通智能强力驱动
Strongly Powered by AbleSci AI