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Interferon-γ liposome: a new system to improve drug delivery in the treatment of lung cancer
Lung cancer is one of the main causes of death worldwide. Published data show the use of interferons (IFNs) in treating lung tumours. IFNs also have potential for their antiproliferative, antiangiogenic, immunoregulatory and proapoptotic effects. IFN-γ functions as an anticancer agent against variou...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381253/ https://www.ncbi.nlm.nih.gov/pubmed/34435034 http://dx.doi.org/10.1183/23120541.00555-2020 |
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author | Alhawmdeh, Maysa Isreb, Mohammad Aziz, Abid Jacob, Badie K. Anderson, Diana Najafzadeh, Mojgan |
author_facet | Alhawmdeh, Maysa Isreb, Mohammad Aziz, Abid Jacob, Badie K. Anderson, Diana Najafzadeh, Mojgan |
author_sort | Alhawmdeh, Maysa |
collection | PubMed |
description | Lung cancer is one of the main causes of death worldwide. Published data show the use of interferons (IFNs) in treating lung tumours. IFNs also have potential for their antiproliferative, antiangiogenic, immunoregulatory and proapoptotic effects. IFN-γ functions as an anticancer agent against various forms of cancer. This study aimed to investigate the effect of IFN-γ liposome (nano) on peripheral lymphocytes from 20 individuals in each group: lung cancer patients compared to healthy individuals. The effectiveness of IFN-γ liposome against oxidative stress was also evaluated in this study. A concentration of 100 U·mL(−1) of IFN-γ liposome was used to treat the lymphocytes in the Comet and micronucleus assays based on the preliminary test for the optimal dose. The lymphocytes from lung cancer patients presented with higher DNA damage levels than those of healthy individuals. In healthy individuals, IFN-γ liposome did not cause any DNA damage in the lymphocytes. Also, it caused a significant reduction in DNA damage in the lymphocytes from lung cancer patients in both the Comet and micronucleus assays. The 100 U·mL(−1) of IFN-γ liposome significantly reduced the oxidative stress caused by H(2)O(2) and appeared to be effective in both groups using the Comet and micronucleus assays. Results from both Comet and micronucleus assays were consistent. The data obtained indicated that IFN-γ in both forms (IFN-γ bulk and IFN-γ nanoliposome) may potentially be effective for the treatment of lung cancer and showed the ability of IFN-γ liposome to reduce DNA damage more than the bulk form. |
format | Online Article Text |
id | pubmed-8381253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | European Respiratory Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83812532021-08-24 Interferon-γ liposome: a new system to improve drug delivery in the treatment of lung cancer Alhawmdeh, Maysa Isreb, Mohammad Aziz, Abid Jacob, Badie K. Anderson, Diana Najafzadeh, Mojgan ERJ Open Res Original Research Articles Lung cancer is one of the main causes of death worldwide. Published data show the use of interferons (IFNs) in treating lung tumours. IFNs also have potential for their antiproliferative, antiangiogenic, immunoregulatory and proapoptotic effects. IFN-γ functions as an anticancer agent against various forms of cancer. This study aimed to investigate the effect of IFN-γ liposome (nano) on peripheral lymphocytes from 20 individuals in each group: lung cancer patients compared to healthy individuals. The effectiveness of IFN-γ liposome against oxidative stress was also evaluated in this study. A concentration of 100 U·mL(−1) of IFN-γ liposome was used to treat the lymphocytes in the Comet and micronucleus assays based on the preliminary test for the optimal dose. The lymphocytes from lung cancer patients presented with higher DNA damage levels than those of healthy individuals. In healthy individuals, IFN-γ liposome did not cause any DNA damage in the lymphocytes. Also, it caused a significant reduction in DNA damage in the lymphocytes from lung cancer patients in both the Comet and micronucleus assays. The 100 U·mL(−1) of IFN-γ liposome significantly reduced the oxidative stress caused by H(2)O(2) and appeared to be effective in both groups using the Comet and micronucleus assays. Results from both Comet and micronucleus assays were consistent. The data obtained indicated that IFN-γ in both forms (IFN-γ bulk and IFN-γ nanoliposome) may potentially be effective for the treatment of lung cancer and showed the ability of IFN-γ liposome to reduce DNA damage more than the bulk form. European Respiratory Society 2021-08-23 /pmc/articles/PMC8381253/ /pubmed/34435034 http://dx.doi.org/10.1183/23120541.00555-2020 Text en Copyright ©The authors 2021 https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org) |
spellingShingle | Original Research Articles Alhawmdeh, Maysa Isreb, Mohammad Aziz, Abid Jacob, Badie K. Anderson, Diana Najafzadeh, Mojgan Interferon-γ liposome: a new system to improve drug delivery in the treatment of lung cancer |
title | Interferon-γ liposome: a new system to improve drug delivery in the treatment of lung cancer |
title_full | Interferon-γ liposome: a new system to improve drug delivery in the treatment of lung cancer |
title_fullStr | Interferon-γ liposome: a new system to improve drug delivery in the treatment of lung cancer |
title_full_unstemmed | Interferon-γ liposome: a new system to improve drug delivery in the treatment of lung cancer |
title_short | Interferon-γ liposome: a new system to improve drug delivery in the treatment of lung cancer |
title_sort | interferon-γ liposome: a new system to improve drug delivery in the treatment of lung cancer |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381253/ https://www.ncbi.nlm.nih.gov/pubmed/34435034 http://dx.doi.org/10.1183/23120541.00555-2020 |
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