A Versatile Multidrug Coloaded Nanoplatform Integrating Photothermal-Differentiation-Chemotherapy for Breast Cancer Stemness Inhibition.
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 penetrat
APA
Pan X, Zhu S, et al. (2026). A Versatile Multidrug Coloaded Nanoplatform Integrating Photothermal-Differentiation-Chemotherapy for Breast Cancer Stemness Inhibition.. Biomacromolecules, 27(2), 1247-1259. https://doi.org/10.1021/acs.biomac.5c01675
MLA
Pan X, et al.. "A Versatile Multidrug Coloaded Nanoplatform Integrating Photothermal-Differentiation-Chemotherapy for Breast Cancer Stemness Inhibition.." Biomacromolecules, vol. 27, no. 2, 2026, pp. 1247-1259.
PMID
41510767
Abstract
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.
MeSH Terms
Humans; Doxorubicin; Neoplastic Stem Cells; Female; Breast Neoplasms; Animals; Hyaluronic Acid; Mice; Cell Differentiation; Photothermal Therapy; Indocyanine Green; Tretinoin; Cell Line, Tumor; Mice, Inbred BALB C; MCF-7 Cells; Mice, Nude; Hyaluronan Receptors; Nanoparticles; Drug Liberation; Antineoplastic Agents
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