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Synergistic Enhancement of Cancer Therapy Using a Combination of Ceramide and Docetaxel
Ceramide (CE)-based combination therapy (CE combination) as a novel therapeutic strategy has attracted great attention in the field of anti-cancer therapy. The principal purposes of this study were to investigate the synergistic effect of CE in combination with docetaxel (DTX) (CE + DTX) and to expl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975392/ https://www.ncbi.nlm.nih.gov/pubmed/24619193 http://dx.doi.org/10.3390/ijms15034201 |
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author | Feng, Li-Xia Li, Min Liu, Yong-Jun Yang, Shao-Mei Zhang, Na |
author_facet | Feng, Li-Xia Li, Min Liu, Yong-Jun Yang, Shao-Mei Zhang, Na |
author_sort | Feng, Li-Xia |
collection | PubMed |
description | Ceramide (CE)-based combination therapy (CE combination) as a novel therapeutic strategy has attracted great attention in the field of anti-cancer therapy. The principal purposes of this study were to investigate the synergistic effect of CE in combination with docetaxel (DTX) (CE + DTX) and to explore the synergy mechanisms of CE + DTX. The 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and combination index (CI) assay showed that simultaneous administration of CE and DTX with a molar ratio of 0.5:1 could generate the optimal synergistic effect on murine malignant melanoma cell (B16, CI = 0.31) and human breast carcinoma cell (MCF-7, CI = 0.48). The apoptosis, cell cycle, and cytoskeleton destruction study demonstrated that CE could target and destruct the microfilament actin, subsequently activate Caspase-3 and induce apoptosis. Meanwhile, DTX could target and disrupt the microtubules cytoskeleton, leading to a high proportion of cancer cells in G2/M-phase arrest. Moreover, CE plus DTX could cause a synergistic destruction of cytoskeleton, which resulted in a significantly higher apoptosis and a significantly higher arrest in G2/M arrest comparing with either agent alone (p < 0.01). The in vivo antitumor study evaluated in B16 tumor-bearing mice also validated the synergistic effects. All these results suggested that CE could enhance the antitumor activity of DTX in a synergistic manner, which suggest promising application prospects of CE + DTX combination treatment. |
format | Online Article Text |
id | pubmed-3975392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-39753922014-04-04 Synergistic Enhancement of Cancer Therapy Using a Combination of Ceramide and Docetaxel Feng, Li-Xia Li, Min Liu, Yong-Jun Yang, Shao-Mei Zhang, Na Int J Mol Sci Article Ceramide (CE)-based combination therapy (CE combination) as a novel therapeutic strategy has attracted great attention in the field of anti-cancer therapy. The principal purposes of this study were to investigate the synergistic effect of CE in combination with docetaxel (DTX) (CE + DTX) and to explore the synergy mechanisms of CE + DTX. The 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and combination index (CI) assay showed that simultaneous administration of CE and DTX with a molar ratio of 0.5:1 could generate the optimal synergistic effect on murine malignant melanoma cell (B16, CI = 0.31) and human breast carcinoma cell (MCF-7, CI = 0.48). The apoptosis, cell cycle, and cytoskeleton destruction study demonstrated that CE could target and destruct the microfilament actin, subsequently activate Caspase-3 and induce apoptosis. Meanwhile, DTX could target and disrupt the microtubules cytoskeleton, leading to a high proportion of cancer cells in G2/M-phase arrest. Moreover, CE plus DTX could cause a synergistic destruction of cytoskeleton, which resulted in a significantly higher apoptosis and a significantly higher arrest in G2/M arrest comparing with either agent alone (p < 0.01). The in vivo antitumor study evaluated in B16 tumor-bearing mice also validated the synergistic effects. All these results suggested that CE could enhance the antitumor activity of DTX in a synergistic manner, which suggest promising application prospects of CE + DTX combination treatment. Molecular Diversity Preservation International (MDPI) 2014-03-10 /pmc/articles/PMC3975392/ /pubmed/24619193 http://dx.doi.org/10.3390/ijms15034201 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Feng, Li-Xia Li, Min Liu, Yong-Jun Yang, Shao-Mei Zhang, Na Synergistic Enhancement of Cancer Therapy Using a Combination of Ceramide and Docetaxel |
title | Synergistic Enhancement of Cancer Therapy Using a Combination of Ceramide and Docetaxel |
title_full | Synergistic Enhancement of Cancer Therapy Using a Combination of Ceramide and Docetaxel |
title_fullStr | Synergistic Enhancement of Cancer Therapy Using a Combination of Ceramide and Docetaxel |
title_full_unstemmed | Synergistic Enhancement of Cancer Therapy Using a Combination of Ceramide and Docetaxel |
title_short | Synergistic Enhancement of Cancer Therapy Using a Combination of Ceramide and Docetaxel |
title_sort | synergistic enhancement of cancer therapy using a combination of ceramide and docetaxel |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975392/ https://www.ncbi.nlm.nih.gov/pubmed/24619193 http://dx.doi.org/10.3390/ijms15034201 |
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