Co-delivery of all-trans-retinoic acid and doxorubicin for cancer therapy with synergistic inhibition of cancer stem cells
Abstract
Combination treatment through simultaneous delivery of two or more drugs with nanoparticles has been demonstrated to be an elegant and efficient approach for cancer therapy. Herein, we employ a combination therapy for eliminating both the bulk tumor cells and the rare cancer stem cells (CSCs) that have a high self-renewal capacity and play a critical role in cancer treatment failure. All-trans-retinoic acid (ATRA), a powerful differentiation agent of cancer stem cells and the clinically widely used chemotherapy agent doxorubicin (DOX) are simultaneously encapsulated in the same nanoparticle by a single emulsion method. It is demonstrated that ATRA and DOX simultaneous delivery-based therapy can efficiently deliver the drugs to both non-CSCs and CSCs to differentiate and kill the cancer cells. Differentiation of CSCs into non-CSCs can reduce their self-renewal capacity and increase their sensitivity to chemotherapy; with the combined therapy, a significantly improved anti-cancer effect is demonstrated. Administration of this combinational drug delivery system can markedly augment the enrichment of drugs both in tumor tissues and cancer stem cells, prodigiously enhancing the suppression of tumor growth while reduce the incidence of CSC in a synergistic manner.
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ATRA liposomes and nanoparticles encapsulating simultaneously ATRA and doxorubicin have been used successfully to arrest the proliferation of breast cancer-initiating cells and to differentiate them.
“ATRA liposomes and nanoparticles encapsulating simultaneously ATRA and doxorubicin have been used successfully to arrest the proliferation of breast cancer-initiating cells and to differentiate them113,114.”
From Advances and challenges in retinoid delivery systems in regenerative and therapeutic medicine (2020) · cites this paper as [114]
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References 57 · Cited by 172
- Authors
- Sun, R., Liu, Y., Li, S.-Y., Shen, S., Du, X.-J., Xu, C.-F., Cao, Z.-T., Bao, Y., Zhu, Y.-H., Li, Y.-P., Yang, X.-Z., & Wang, J.
- Affiliations
- University of Science and Technology of China (CN)
- Corresponding author
- Wang, Jun
- Venue
- Biomaterials
- Publisher
- Elsevier BV
- Published
- 2015-01
- Volume
- 37
- Pages
- 405-414
- ISSN
- 0142-9612 (ISSN-L)
- OpenAlex
- W1981599964
- Cited by
- 172
- References
- 57
- Citations by year
- 2026: 5 · 2025: 10 · 2024: 14 · 2023: 14 · 2022: 13 · 2021: 16 · 2020: 22 · 2019: 22 · 2018: 18 · 2017: 21 · 2016: 8 · 2015: 9
- FWCI
- 4.79
- Type
- journal article
- Language
- en
- Update notices
- erratum (2020-12-01)
- Open access
- closed
- Locations
- Biomaterials (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Basic Research Program of China (2010CB934001, 2013CB933900, 2012CB932500)
- National Natural Science Foundation of China (31470965, 51125012, 51390482)
- State Key Laboratory of Supramolecular Structure and Materials (sklssm201413)
- Topics
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Physical Sciences › Engineering › Biomedical Engineering › Nanoplatforms for cancer theranostics
- Keywords
- all-trans retinoic acid, doxorubicin, cancer stem cells, combination drug delivery, nanoparticle drug delivery, co-delivery, tumor cell differentiation, self-renewal, tumor growth inhibition, synergistic cancer therapy
- MeSH terms
- Animals, Breast Neoplasms, Cell Differentiation, Doxorubicin, Drug Synergism, Female, Humans, Injections, Intravenous, Neoplasms, Particle Size, Tretinoin, Neoplastic Stem Cells, Gene Expression Regulation, Neoplastic, Drug Delivery Systems, Mice, SCID, Mice, Inbred NOD, Proliferating Cell Nuclear Antigen, Cell Line, Tumor, Cell Proliferation, Nanoparticles, Static Electricity
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