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A Versatile Multidrug Coloaded Nanoplatform Integrating Photothermal-Differentiation-Chemotherapy for Breast Cancer Stemness Inhibition.

Biomacromolecules 2026 Vol.27(2) p. 1247-1259

Pan X, Zhu S, Cu W, Jin L, Chen J, Zhang X, Zhang W, Wang T

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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

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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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