CD123-Targeted Nano-Curcumin Molecule Enhances Cytotoxic Efficacy in Leukemic Stem Cells
Acute myeloblastic leukemia (AML) is a disease with a high rate of relapse and drug resistance due to the remaining leukemic stem cells (LSCs). Therefore, LSCs are specific targets for the treatment of leukemia. CD123 is specifically expressed on LSCs and performs as a specific marker. Curcumin is t...
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2021
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oai:doaj.org-article:1060137960654519a4dd0b09051af9732021-11-25T18:31:21ZCD123-Targeted Nano-Curcumin Molecule Enhances Cytotoxic Efficacy in Leukemic Stem Cells10.3390/nano111129742079-4991https://doaj.org/article/1060137960654519a4dd0b09051af9732021-11-01T00:00:00Zhttps://www.mdpi.com/2079-4991/11/11/2974https://doaj.org/toc/2079-4991Acute myeloblastic leukemia (AML) is a disease with a high rate of relapse and drug resistance due to the remaining leukemic stem cells (LSCs). Therefore, LSCs are specific targets for the treatment of leukemia. CD123 is specifically expressed on LSCs and performs as a specific marker. Curcumin is the main active compound of a natural product with low toxicity for humans. It has been reported to inhibit leukemic cell growth. However, curcumin is practically insoluble in water and has low bioavailability. In this study, we aimed to formulate curcumin nanoparticles and conjugate with the anti-CD123 to overcome the low water solubility and improve the targeting of LSCs. The cytotoxicity of both curcumin-loaded PLGA/poloxamer nanoparticles (Cur-NPs) and anti-CD123-curcumin-loaded PLGA/poloxamer nanoparticles (anti-CD123-Cur-NPs) were examined in KG-1a cells. The results showed that Cur-NPs and Cur-NPs-CD123 exhibited cytotoxic effects on KG-1a cells with the IC<sub>50</sub> values of 74.20 ± 6.71 and 41.45 ± 5.49 µM, respectively. Moreover, anti-CD123-Cur-NPs induced higher apoptosis than Cur-NPs. The higher uptake of anti-CD123-Cur-NPs in KG-1a cells was confirmed by using flow cytometry. In conclusion, the anti-CD123-Cur-NPs formulation improved curcumin’s bioavailability and specific targeting of LSCs, suggesting that it is a promising drug delivery system for improving the therapeutic efficacy against AML.Wariya NirachonkulSiriporn OgonokiTarika ThumvijitSupanimit ChiampanichayakulPawaret PanyajaiSongyot AnuchapreedaSingkome TimaSawitree ChiampanichayakulMDPI AGarticleanti-CD123leukemic stem cellscurcuminacute myeloblastic leukemiananoparticlesChemistryQD1-999ENNanomaterials, Vol 11, Iss 2974, p 2974 (2021) |
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anti-CD123 leukemic stem cells curcumin acute myeloblastic leukemia nanoparticles Chemistry QD1-999 |
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anti-CD123 leukemic stem cells curcumin acute myeloblastic leukemia nanoparticles Chemistry QD1-999 Wariya Nirachonkul Siriporn Ogonoki Tarika Thumvijit Supanimit Chiampanichayakul Pawaret Panyajai Songyot Anuchapreeda Singkome Tima Sawitree Chiampanichayakul CD123-Targeted Nano-Curcumin Molecule Enhances Cytotoxic Efficacy in Leukemic Stem Cells |
description |
Acute myeloblastic leukemia (AML) is a disease with a high rate of relapse and drug resistance due to the remaining leukemic stem cells (LSCs). Therefore, LSCs are specific targets for the treatment of leukemia. CD123 is specifically expressed on LSCs and performs as a specific marker. Curcumin is the main active compound of a natural product with low toxicity for humans. It has been reported to inhibit leukemic cell growth. However, curcumin is practically insoluble in water and has low bioavailability. In this study, we aimed to formulate curcumin nanoparticles and conjugate with the anti-CD123 to overcome the low water solubility and improve the targeting of LSCs. The cytotoxicity of both curcumin-loaded PLGA/poloxamer nanoparticles (Cur-NPs) and anti-CD123-curcumin-loaded PLGA/poloxamer nanoparticles (anti-CD123-Cur-NPs) were examined in KG-1a cells. The results showed that Cur-NPs and Cur-NPs-CD123 exhibited cytotoxic effects on KG-1a cells with the IC<sub>50</sub> values of 74.20 ± 6.71 and 41.45 ± 5.49 µM, respectively. Moreover, anti-CD123-Cur-NPs induced higher apoptosis than Cur-NPs. The higher uptake of anti-CD123-Cur-NPs in KG-1a cells was confirmed by using flow cytometry. In conclusion, the anti-CD123-Cur-NPs formulation improved curcumin’s bioavailability and specific targeting of LSCs, suggesting that it is a promising drug delivery system for improving the therapeutic efficacy against AML. |
format |
article |
author |
Wariya Nirachonkul Siriporn Ogonoki Tarika Thumvijit Supanimit Chiampanichayakul Pawaret Panyajai Songyot Anuchapreeda Singkome Tima Sawitree Chiampanichayakul |
author_facet |
Wariya Nirachonkul Siriporn Ogonoki Tarika Thumvijit Supanimit Chiampanichayakul Pawaret Panyajai Songyot Anuchapreeda Singkome Tima Sawitree Chiampanichayakul |
author_sort |
Wariya Nirachonkul |
title |
CD123-Targeted Nano-Curcumin Molecule Enhances Cytotoxic Efficacy in Leukemic Stem Cells |
title_short |
CD123-Targeted Nano-Curcumin Molecule Enhances Cytotoxic Efficacy in Leukemic Stem Cells |
title_full |
CD123-Targeted Nano-Curcumin Molecule Enhances Cytotoxic Efficacy in Leukemic Stem Cells |
title_fullStr |
CD123-Targeted Nano-Curcumin Molecule Enhances Cytotoxic Efficacy in Leukemic Stem Cells |
title_full_unstemmed |
CD123-Targeted Nano-Curcumin Molecule Enhances Cytotoxic Efficacy in Leukemic Stem Cells |
title_sort |
cd123-targeted nano-curcumin molecule enhances cytotoxic efficacy in leukemic stem cells |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/1060137960654519a4dd0b09051af973 |
work_keys_str_mv |
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