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Effect of interaction of magnetic nanoparticles of Fe(3)O(4) and artesunate on apoptosis of K562 cells

The present study evaluated whether the magnetic nanoparticles of Fe(3)O(4) (MNPs-Fe(3)O(4)) could enhance the activity of artesunate (ART), and to explore its potential mechanisms. Cytotoxicity of the copolymer of ART with MNPs-Fe(3)O(4) on K562 cells was detected by MTT assay and the apoptosis rat...

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Autores principales: Wang, Ying, Han, Yuxiang, Yang, Yingying, Yang, Jingci, Guo, Xiaonan, Zhang, Jingnan, Pan, Ling, Xia, Guohua, Chen, Baoan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148844/
https://www.ncbi.nlm.nih.gov/pubmed/21822380
http://dx.doi.org/10.2147/IJN.S19723
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author Wang, Ying
Han, Yuxiang
Yang, Yingying
Yang, Jingci
Guo, Xiaonan
Zhang, Jingnan
Pan, Ling
Xia, Guohua
Chen, Baoan
author_facet Wang, Ying
Han, Yuxiang
Yang, Yingying
Yang, Jingci
Guo, Xiaonan
Zhang, Jingnan
Pan, Ling
Xia, Guohua
Chen, Baoan
author_sort Wang, Ying
collection PubMed
description The present study evaluated whether the magnetic nanoparticles of Fe(3)O(4) (MNPs-Fe(3)O(4)) could enhance the activity of artesunate (ART), and to explore its potential mechanisms. Cytotoxicity of the copolymer of ART with MNPs-Fe(3)O(4) on K562 cells was detected by MTT assay and the apoptosis rate of K562 cells was measured by flow cytometry. Protein expression levels of bcl-2, bax, bcl-rambo, caspase-3, and survivin in K562 cells were measured by Western blot. After being incubated with the copolymer of ART with MNPs-Fe(3)O(4) for 48 hours, the growth inhibition rate of K562 cells was significantly increased compared with that of K562 cells treated with ART alone (P < 0.05), and the apoptosis rate of K562 cells was increased significantly compared with that of K562 cells treated with ART alone, suggesting that MNPs-Fe(3)O(4) can enhance the activity of ART. Interestingly, the copolymer-induced cell death was attenuated by caspase inhibitor Z-VAD-FMK. Our results also showed that treatment with the copolymer of MNPs-Fe(3)O(4) and ART increased the expression of bcl-2, bax, bcl-rambo, and caspase-3 proteins, and decreased the expression of survivin protein in K562 cells compared with ART treatment alone. These results suggest that MNPs-Fe(3)O(4) can enhance ART-induced apoptosis, which may be related to the upregulation of bcl-rambo and downregulation of survivin.
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spelling pubmed-31488442011-08-05 Effect of interaction of magnetic nanoparticles of Fe(3)O(4) and artesunate on apoptosis of K562 cells Wang, Ying Han, Yuxiang Yang, Yingying Yang, Jingci Guo, Xiaonan Zhang, Jingnan Pan, Ling Xia, Guohua Chen, Baoan Int J Nanomedicine Original Research The present study evaluated whether the magnetic nanoparticles of Fe(3)O(4) (MNPs-Fe(3)O(4)) could enhance the activity of artesunate (ART), and to explore its potential mechanisms. Cytotoxicity of the copolymer of ART with MNPs-Fe(3)O(4) on K562 cells was detected by MTT assay and the apoptosis rate of K562 cells was measured by flow cytometry. Protein expression levels of bcl-2, bax, bcl-rambo, caspase-3, and survivin in K562 cells were measured by Western blot. After being incubated with the copolymer of ART with MNPs-Fe(3)O(4) for 48 hours, the growth inhibition rate of K562 cells was significantly increased compared with that of K562 cells treated with ART alone (P < 0.05), and the apoptosis rate of K562 cells was increased significantly compared with that of K562 cells treated with ART alone, suggesting that MNPs-Fe(3)O(4) can enhance the activity of ART. Interestingly, the copolymer-induced cell death was attenuated by caspase inhibitor Z-VAD-FMK. Our results also showed that treatment with the copolymer of MNPs-Fe(3)O(4) and ART increased the expression of bcl-2, bax, bcl-rambo, and caspase-3 proteins, and decreased the expression of survivin protein in K562 cells compared with ART treatment alone. These results suggest that MNPs-Fe(3)O(4) can enhance ART-induced apoptosis, which may be related to the upregulation of bcl-rambo and downregulation of survivin. Dove Medical Press 2011 2011-06-09 /pmc/articles/PMC3148844/ /pubmed/21822380 http://dx.doi.org/10.2147/IJN.S19723 Text en © 2011 Wang et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Wang, Ying
Han, Yuxiang
Yang, Yingying
Yang, Jingci
Guo, Xiaonan
Zhang, Jingnan
Pan, Ling
Xia, Guohua
Chen, Baoan
Effect of interaction of magnetic nanoparticles of Fe(3)O(4) and artesunate on apoptosis of K562 cells
title Effect of interaction of magnetic nanoparticles of Fe(3)O(4) and artesunate on apoptosis of K562 cells
title_full Effect of interaction of magnetic nanoparticles of Fe(3)O(4) and artesunate on apoptosis of K562 cells
title_fullStr Effect of interaction of magnetic nanoparticles of Fe(3)O(4) and artesunate on apoptosis of K562 cells
title_full_unstemmed Effect of interaction of magnetic nanoparticles of Fe(3)O(4) and artesunate on apoptosis of K562 cells
title_short Effect of interaction of magnetic nanoparticles of Fe(3)O(4) and artesunate on apoptosis of K562 cells
title_sort effect of interaction of magnetic nanoparticles of fe(3)o(4) and artesunate on apoptosis of k562 cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148844/
https://www.ncbi.nlm.nih.gov/pubmed/21822380
http://dx.doi.org/10.2147/IJN.S19723
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