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Synergistic Effects of Melittin and Plasma Treatment: A Promising Approach for Cancer Therapy
Melittin (MEL), a small peptide component of bee venom, has been reported to exhibit anti-cancer effects in vitro and in vivo. However, its clinical applicability is disputed because of its non-specific cytotoxicity and haemolytic activity in high treatment doses. Plasma-treated phosphate buffered s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721819/ https://www.ncbi.nlm.nih.gov/pubmed/31382579 http://dx.doi.org/10.3390/cancers11081109 |
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author | Shaw, Priyanka Kumar, Naresh Hammerschmid, Dietmar Privat-Maldonado, Angela Dewilde, Sylvia Bogaerts, Annemie |
author_facet | Shaw, Priyanka Kumar, Naresh Hammerschmid, Dietmar Privat-Maldonado, Angela Dewilde, Sylvia Bogaerts, Annemie |
author_sort | Shaw, Priyanka |
collection | PubMed |
description | Melittin (MEL), a small peptide component of bee venom, has been reported to exhibit anti-cancer effects in vitro and in vivo. However, its clinical applicability is disputed because of its non-specific cytotoxicity and haemolytic activity in high treatment doses. Plasma-treated phosphate buffered saline solution (PT-PBS), a solution rich in reactive oxygen and nitrogen species (RONS) can disrupt the cell membrane integrity and induce cancer cell death through oxidative stress-mediated pathways. Thus, PT-PBS could be used in combination with MEL to facilitate its access into cancer cells and to reduce the required therapeutic dose. The aim of our study is to determine the reduction of the effective dose of MEL required to eliminate cancer cells by its combination with PT-PBS. For this purpose, we have optimised the MEL threshold concentration and tested the combined treatment of MEL and PT-PBS on A375 melanoma and MCF7 breast cancer cells, using in vitro, in ovo and in silico approaches. We investigated the cytotoxic effect of MEL and PT-PBS alone and in combination to reveal their synergistic cytological effects. To support the in vitro and in ovo experiments, we showed by computer simulations that plasma-induced oxidation of the phospholipid bilayer leads to a decrease of the free energy barrier for translocation of MEL in comparison with the non-oxidized bilayer, which also suggests a synergistic effect of MEL with plasma induced oxidation. Overall, our findings suggest that MEL in combination with PT-PBS can be a promising combinational therapy to circumvent the non-specific toxicity of MEL, which may help for clinical applicability in the future. |
format | Online Article Text |
id | pubmed-6721819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67218192019-09-10 Synergistic Effects of Melittin and Plasma Treatment: A Promising Approach for Cancer Therapy Shaw, Priyanka Kumar, Naresh Hammerschmid, Dietmar Privat-Maldonado, Angela Dewilde, Sylvia Bogaerts, Annemie Cancers (Basel) Article Melittin (MEL), a small peptide component of bee venom, has been reported to exhibit anti-cancer effects in vitro and in vivo. However, its clinical applicability is disputed because of its non-specific cytotoxicity and haemolytic activity in high treatment doses. Plasma-treated phosphate buffered saline solution (PT-PBS), a solution rich in reactive oxygen and nitrogen species (RONS) can disrupt the cell membrane integrity and induce cancer cell death through oxidative stress-mediated pathways. Thus, PT-PBS could be used in combination with MEL to facilitate its access into cancer cells and to reduce the required therapeutic dose. The aim of our study is to determine the reduction of the effective dose of MEL required to eliminate cancer cells by its combination with PT-PBS. For this purpose, we have optimised the MEL threshold concentration and tested the combined treatment of MEL and PT-PBS on A375 melanoma and MCF7 breast cancer cells, using in vitro, in ovo and in silico approaches. We investigated the cytotoxic effect of MEL and PT-PBS alone and in combination to reveal their synergistic cytological effects. To support the in vitro and in ovo experiments, we showed by computer simulations that plasma-induced oxidation of the phospholipid bilayer leads to a decrease of the free energy barrier for translocation of MEL in comparison with the non-oxidized bilayer, which also suggests a synergistic effect of MEL with plasma induced oxidation. Overall, our findings suggest that MEL in combination with PT-PBS can be a promising combinational therapy to circumvent the non-specific toxicity of MEL, which may help for clinical applicability in the future. MDPI 2019-08-03 /pmc/articles/PMC6721819/ /pubmed/31382579 http://dx.doi.org/10.3390/cancers11081109 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shaw, Priyanka Kumar, Naresh Hammerschmid, Dietmar Privat-Maldonado, Angela Dewilde, Sylvia Bogaerts, Annemie Synergistic Effects of Melittin and Plasma Treatment: A Promising Approach for Cancer Therapy |
title | Synergistic Effects of Melittin and Plasma Treatment: A Promising Approach for Cancer Therapy |
title_full | Synergistic Effects of Melittin and Plasma Treatment: A Promising Approach for Cancer Therapy |
title_fullStr | Synergistic Effects of Melittin and Plasma Treatment: A Promising Approach for Cancer Therapy |
title_full_unstemmed | Synergistic Effects of Melittin and Plasma Treatment: A Promising Approach for Cancer Therapy |
title_short | Synergistic Effects of Melittin and Plasma Treatment: A Promising Approach for Cancer Therapy |
title_sort | synergistic effects of melittin and plasma treatment: a promising approach for cancer therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721819/ https://www.ncbi.nlm.nih.gov/pubmed/31382579 http://dx.doi.org/10.3390/cancers11081109 |
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