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Magnetic nanoparticles of Fe(3)O(4) enhance docetaxel-induced prostate cancer cell death
Docetaxel (DTX) is one of the most important anticancer drugs; however, the severity of its adverse effects detracts from its practical use in the clinic. Magnetic nanoparticles of Fe(3)O(4) (MgNPs-Fe(3)O(4)) can enhance the delivery and efficacy of anticancer drugs. We investigated the effects of M...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753150/ https://www.ncbi.nlm.nih.gov/pubmed/23990723 http://dx.doi.org/10.2147/IJN.S40766 |
Sumario: | Docetaxel (DTX) is one of the most important anticancer drugs; however, the severity of its adverse effects detracts from its practical use in the clinic. Magnetic nanoparticles of Fe(3)O(4) (MgNPs-Fe(3)O(4)) can enhance the delivery and efficacy of anticancer drugs. We investigated the effects of MgNPs-Fe(3)O(4) or DTX alone, and in combination with prostate cancer cell growth in vitro, as well as with the mechanism underlying the cytotoxic effects. MgNPs-Fe(3)O(4) caused dose-dependent increases in reactive oxygen species levels in DU145, PC-3, and LNCaP cells; 8-hydroxydeoxyguanosine levels were also elevated. MgNPs-Fe(3)O(4) alone reduced the viability of LNCaP and PC-3 cells; however, MgNPs-Fe(3)O(4) enhanced the cytotoxic effect of a low dose of DTX in all three cell lines. MgNPs-Fe(3)O(4) also augmented the percentage of DU145 cells undergoing apoptosis following treatment with low dose DTX. Expression of nuclear transcription factor κB in DU145 was not affected by MgNPs-Fe(3)O(4) or DTX alone; however, combined treatment suppressed nuclear transcription factor κB expression. These findings offer the possibility that MgNPs-Fe(3)O(4)–low dose DTX combination therapy may be effective in treating prostate cancer with limited adverse effects. |
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