Cited by 172Nanoparticle-Based Drug DeliveryCancer Cells and MetastasisNanoplatforms for cancer theranostics

Co-delivery of all-trans-retinoic acid and doxorubicin for cancer therapy with synergistic inhibition of cancer stem cells

Sun, Rong, Liu, Yang, Li, Shi-Yong, Shen, Song, Du, Xiao-Jiao, Xu, Cong-Fei, Cao, Zhi-Ting, Bao, Yan +4 more·2015·Biomaterials

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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Crossref · 10.1016/j.biomaterials.2014.10.018

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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.”

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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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