Efficient tailoring of platinum nanoparticles supported on multiwalled carbon nanotubes for cancer therapy
Therapeutically targeting cancer stem cells (CSCs), which play a role in tumor initiation and relapse, remains challenging. Novel-formulated platinum nanoparticles (Pt-NPs) supported on polybenzimidazole (PBI)-functionalized polymers and multiwalled carbon nanotubes (MWCNT) were prepared and their e...
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Veröffentlicht in: | Nanomedicine (London, England) England), 2020-04, Vol.15 (8), p.793-808 |
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Zusammenfassung: | Therapeutically targeting cancer stem cells (CSCs), which play a role in tumor initiation and relapse, remains challenging.
Novel-formulated platinum nanoparticles (Pt-NPs) supported on polybenzimidazole (PBI)-functionalized polymers and multiwalled carbon nanotubes (MWCNT) were prepared and their effect on CSCs was evaluated.
Pt-NPs showed homogenous distribution on the surface of MWCNT/PBI composites, with very narrow particle size. MWCNT/PBI/Pt-NPs resulted in a dramatic decrease in the proliferation rate of CSCs but not bone marrow mesenchymal stem cells (BM-MSCs). Quantitative gene expression analysis revealed that MWCNT/PBI/Pt had a significant inhibitory effect on the epithelial-mesenchymal transition and cell cycle markers of CSCs.
MWCNT/PBI/Pt exhibited a specific cytotoxic effect on breast CSCs but not on adult stem cells.
An
study on the anticancer effect of novel-formulated platinum nanoparticles (Pt-NPs) supported on polybenzimidazole (PBI)-functionalized MWCNT (MWCNT/PBI/Pt-NPs) on human breast cancer stem cells (CSCs). We have demonstrated that the anticancer effect of MWCNT/PBI/Pt on CSCs may have different molecular pathway compared with cisplatin. MWCNT/PBI/Pt could induce cell cycle arrest, reduce drug resistance and inhibit DNA repair properties of breast CSCs. |
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ISSN: | 1743-5889 1748-6963 |
DOI: | 10.2217/nnm-2019-0445 |