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Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy
Hematological malignancies are important diseases that need more powerful therapeutics. Even with current targeting therapies, such as rituximab and other chemotherapeutic agents, there is a need to develop new treatment strategies. Combination therapy seems the best option to target the tumor cells...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996254/ https://www.ncbi.nlm.nih.gov/pubmed/27579294 http://dx.doi.org/10.2147/OV.S95250 |
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author | Al-Shammari, Ahmed Majeed Rameez, Huda Al-Taee, Maha F |
author_facet | Al-Shammari, Ahmed Majeed Rameez, Huda Al-Taee, Maha F |
author_sort | Al-Shammari, Ahmed Majeed |
collection | PubMed |
description | Hematological malignancies are important diseases that need more powerful therapeutics. Even with current targeting therapies, such as rituximab and other chemotherapeutic agents, there is a need to develop new treatment strategies. Combination therapy seems the best option to target the tumor cells by different mechanisms. Virotherapy is a very promising treatment modality, as it is selective, safe, and causes cancer destruction. The Iraqi strain of Newcastle disease virus (NDV) has proved to be effective both in vitro and in vivo. In the current work, we tested its ability on anti-hematological tumors and enhanced current treatments with combination therapy, and studied this combination using Chou–Talalay analysis. p53 concentration was measured to evaluate the mechanism of this proposed synergism. The results showed that NDV was synergistic with doxorubicin in low doses on plasmacytoma cells, with no involvement of p53 pathways, but involved p53 when the combination was used on non-Hodgkin lymphoma cells. NDV in combination with rituximab showed enhanced cytotoxicity that was p53-independent. In conclusion, this work proposes a novel combination modality for treatment of some hematological malignancies. |
format | Online Article Text |
id | pubmed-4996254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49962542016-08-30 Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy Al-Shammari, Ahmed Majeed Rameez, Huda Al-Taee, Maha F Oncolytic Virother Original Research Hematological malignancies are important diseases that need more powerful therapeutics. Even with current targeting therapies, such as rituximab and other chemotherapeutic agents, there is a need to develop new treatment strategies. Combination therapy seems the best option to target the tumor cells by different mechanisms. Virotherapy is a very promising treatment modality, as it is selective, safe, and causes cancer destruction. The Iraqi strain of Newcastle disease virus (NDV) has proved to be effective both in vitro and in vivo. In the current work, we tested its ability on anti-hematological tumors and enhanced current treatments with combination therapy, and studied this combination using Chou–Talalay analysis. p53 concentration was measured to evaluate the mechanism of this proposed synergism. The results showed that NDV was synergistic with doxorubicin in low doses on plasmacytoma cells, with no involvement of p53 pathways, but involved p53 when the combination was used on non-Hodgkin lymphoma cells. NDV in combination with rituximab showed enhanced cytotoxicity that was p53-independent. In conclusion, this work proposes a novel combination modality for treatment of some hematological malignancies. Dove Medical Press 2016-04-20 /pmc/articles/PMC4996254/ /pubmed/27579294 http://dx.doi.org/10.2147/OV.S95250 Text en © 2016 Al-Shammari et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Al-Shammari, Ahmed Majeed Rameez, Huda Al-Taee, Maha F Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy |
title | Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy |
title_full | Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy |
title_fullStr | Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy |
title_full_unstemmed | Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy |
title_short | Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy |
title_sort | newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996254/ https://www.ncbi.nlm.nih.gov/pubmed/27579294 http://dx.doi.org/10.2147/OV.S95250 |
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