癌症研究
透明质酸
光热治疗
多重耐药
体外
化学
癌症干细胞
阿霉素
药品
化疗
乳腺癌
抗药性
干细胞
癌症
癌细胞
药理学
药物输送
肿瘤微环境
体内
靶向给药
治疗指标
癌症治疗
常用化疗药物
癌症治疗
细胞毒性
治疗效果
肿瘤细胞
毒品携带者
医学
作者
Xiangmei Pan,Shan Zhu,Weiwei Cu,Jun Ma,Jianrong Chen,Xiaoyu Zhang,Wei Zhang,Tie Zheng Wang
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2026-01-09
卷期号:27 (2): 1247-1259
标识
DOI:10.1021/acs.biomac.5c01675
摘要
Cancer stem cells (CSCs) are a subpopulation of tumor cells with strong tumorigenic ability and high resistance to conventional therapeutic strategies due to the protected niche and poor drug penetration. While self-assembled nanosystems based on small-molecule self-assembly show therapeutic promise, limitations such as low targeting and unstable drug release still constrain their applications. In this study, we developed CD44-targeted RHID (ICG-DOX@RA-HA-DOX) nanocomplexes with a shell of hyaluronic acid-retinoic acid-doxorubicin (RA-HA-DOX) conjugates and a core of DOX-indocyanine green (ICG), which exhibited sustained and pH-responsive release properties. The released DOX and ICG could synergistically eliminate bulk tumors via chemotherapy and photothermal therapy. Concurrently, the released RA could promote CSC differentiation, further reducing stemness, self-renewal, and mammosphere formation, thereby enhancing the therapeutic sensitivity of CSCs to combined therapy. This integrated photothermal-differentiation-chemotherapy approach demonstrated strong antitumor efficacy both in vitro and in vivo, providing a promising nanotherapeutic strategy against CSC-driven malignancies.
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