» Articles » PMID: 38102651

A Polymeric Nanocarrier That Eradicates Breast Cancer Stem Cells and Delivers Chemotherapeutic Drugs

Overview
Journal Biomater Res
Date 2023 Dec 16
PMID 38102651
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Drug nanocarriers can markedly reduce the toxicities and side effects of encapsulated chemotherapeutic drugs in the clinic. However, these drug nanocarriers have little effect on eradicating breast cancer stem cells (BCSCs). Although compounds that can inhibit BCSCs have been reported, these compounds are difficult to use as carriers for the widespread delivery of conventional chemotherapeutic drugs.

Methods: Herein, we synthesize a polymeric nanocarrier, hyaluronic acid-block-poly (curcumin-dithiodipropionic acid) (HA-b-PCDA), and explore the use of HA-b-PCDA to simultaneously deliver chemotherapeutic drugs and eradicate BCSCs.

Results: Based on molecular docking and molecular dynamics studies, HA-b-PCDA delivers 35 clinical chemotherapeutic drugs. To further verify the drug deliver ability of HA-b-PCDA, doxorubicin, paclitaxel, docetaxel, gemcitabine and camptothecin are employed as model drugs to prepare nanoparticles. These drug-loaded HA-b-PCDA nanoparticles significantly inhibit the proliferation and stemness of BCSC-enriched 4T1 mammospheres. Moreover, doxorubicin-loaded HA-b-PCDA nanoparticles efficiently inhibit tumor growth and eradicate approximately 95% of BCSCs fraction in vivo. Finally, HA-b-PCDA eradicates BCSCs by activating Hippo and inhibiting the JAK2/STAT3 pathway.

Conclusion: HA-b-PCDA is a polymeric nanocarrier that eradicates BCSCs and potentially delivers numerous clinical chemotherapeutic drugs.

Citing Articles

Targeted multimodal synergistic therapy of drug-resistant HER2-positive breast cancer by pyrotinib-ICG self-assembled nanoparticles.

Xuhong J, Wu N, Shi Q, Tian H, Peng Z, Jiang J Am J Cancer Res. 2024; 14(8):3976-3993.

PMID: 39267659 PMC: 11387853. DOI: 10.62347/JZRN6919.


The complex interplay of tumor-infiltrating cells in driving therapeutic resistance pathways.

Li D, Shao F, Yu Q, Wu R, Tuo Z, Wang J Cell Commun Signal. 2024; 22(1):405.

PMID: 39160622 PMC: 11331645. DOI: 10.1186/s12964-024-01776-7.


Epigenetic clocks and gliomas: unveiling the molecular interactions between aging and tumor development.

Chen S, Jiang Y, Wang C, Tong S, He Y, Lu W Front Mol Biosci. 2024; 11:1446428.

PMID: 39130373 PMC: 11310061. DOI: 10.3389/fmolb.2024.1446428.

References
1.
Liu Y, Zhu C, Tang L, Chen Q, Guan N, Xu K . MYC dysfunction modulates stemness and tumorigenesis in breast cancer. Int J Biol Sci. 2021; 17(1):178-187. PMC: 7757029. DOI: 10.7150/ijbs.51458. View

2.
Du W, Yang X, He S, Wang J, Guo Y, Kou B . Novel hyaluronic acid oligosaccharide-loaded and CD44v6-targeting oxaliplatin nanoparticles for the treatment of colorectal cancer. Drug Deliv. 2021; 28(1):920-929. PMC: 8118506. DOI: 10.1080/10717544.2021.1914777. View

3.
Lv L, Shi Y, Wu J, Li G . Nanosized Drug Delivery Systems for Breast Cancer Stem Cell Targeting. Int J Nanomedicine. 2021; 16:1487-1508. PMC: 7914063. DOI: 10.2147/IJN.S282110. View

4.
Zou H, Luo J, Guo Y, Liu Y, Wang Y, Deng L . RNA-binding protein complex LIN28/MSI2 enhances cancer stem cell-like properties by modulating Hippo-YAP1 signaling and independently of Let-7. Oncogene. 2022; 41(11):1657-1672. PMC: 8913359. DOI: 10.1038/s41388-022-02198-w. View

5.
Sardao V, Oliveira P, Holy J, Oliveira C, Wallace K . Morphological alterations induced by doxorubicin on H9c2 myoblasts: nuclear, mitochondrial, and cytoskeletal targets. Cell Biol Toxicol. 2008; 25(3):227-43. DOI: 10.1007/s10565-008-9070-1. View