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Anticancer potential of myricetin bulk and nano forms in vitro in lymphocytes from myeloma patients
Evading apoptosis and chemo-resistance are considered as very important factors which help tumour progression and metastasis. Hence, to overcome chemo-resistance, there is an urgent requirement for emergence of more effective treatment options. Myricetin, a naturally occurring flavonoid, is present...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811500/ https://www.ncbi.nlm.nih.gov/pubmed/33128380 http://dx.doi.org/10.1007/s00204-020-02938-5 |
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author | Akhtar, Shabana Najafzadeh, Mojgan Isreb, Mohammad Newton, Lisa Gopalan, Rajendran C. Anderson, Diana |
author_facet | Akhtar, Shabana Najafzadeh, Mojgan Isreb, Mohammad Newton, Lisa Gopalan, Rajendran C. Anderson, Diana |
author_sort | Akhtar, Shabana |
collection | PubMed |
description | Evading apoptosis and chemo-resistance are considered as very important factors which help tumour progression and metastasis. Hence, to overcome chemo-resistance, there is an urgent requirement for emergence of more effective treatment options. Myricetin, a naturally occurring flavonoid, is present in various plant-derived foods and shows antitumour potential in different cancers. In the present in vitro study, results from the comet assay demonstrated that myricetin bulk (10 µM) and nano (20 µM) forms exhibited a non-significant level of genotoxicity in lymphocytes from multiple myeloma patients when compared to those from healthy individuals. Western blot results showed a decrease in Bcl-2/Bax ratio and an increase in P53 protein levels in lymphocytes from myeloma patients, but not in lymphocytes from healthy individuals. A significant increase in intracellular reactive oxygen species level was also observed, suggesting that regulation of apoptotic proteins triggered by myricetin exposure in lymphocytes from myeloma patients occurred through P53 and oxidative stress-dependent pathways. The potency of myricetin against lymphocytes from myeloma patients marks it a potential candidate to be considered as an alternative to overcome chemo-resistance in cancer therapies. |
format | Online Article Text |
id | pubmed-7811500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-78115002021-01-25 Anticancer potential of myricetin bulk and nano forms in vitro in lymphocytes from myeloma patients Akhtar, Shabana Najafzadeh, Mojgan Isreb, Mohammad Newton, Lisa Gopalan, Rajendran C. Anderson, Diana Arch Toxicol Genotoxicity and Carcinogenicity Evading apoptosis and chemo-resistance are considered as very important factors which help tumour progression and metastasis. Hence, to overcome chemo-resistance, there is an urgent requirement for emergence of more effective treatment options. Myricetin, a naturally occurring flavonoid, is present in various plant-derived foods and shows antitumour potential in different cancers. In the present in vitro study, results from the comet assay demonstrated that myricetin bulk (10 µM) and nano (20 µM) forms exhibited a non-significant level of genotoxicity in lymphocytes from multiple myeloma patients when compared to those from healthy individuals. Western blot results showed a decrease in Bcl-2/Bax ratio and an increase in P53 protein levels in lymphocytes from myeloma patients, but not in lymphocytes from healthy individuals. A significant increase in intracellular reactive oxygen species level was also observed, suggesting that regulation of apoptotic proteins triggered by myricetin exposure in lymphocytes from myeloma patients occurred through P53 and oxidative stress-dependent pathways. The potency of myricetin against lymphocytes from myeloma patients marks it a potential candidate to be considered as an alternative to overcome chemo-resistance in cancer therapies. Springer Berlin Heidelberg 2020-10-30 2021 /pmc/articles/PMC7811500/ /pubmed/33128380 http://dx.doi.org/10.1007/s00204-020-02938-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Genotoxicity and Carcinogenicity Akhtar, Shabana Najafzadeh, Mojgan Isreb, Mohammad Newton, Lisa Gopalan, Rajendran C. Anderson, Diana Anticancer potential of myricetin bulk and nano forms in vitro in lymphocytes from myeloma patients |
title | Anticancer potential of myricetin bulk and nano forms in vitro in lymphocytes from myeloma patients |
title_full | Anticancer potential of myricetin bulk and nano forms in vitro in lymphocytes from myeloma patients |
title_fullStr | Anticancer potential of myricetin bulk and nano forms in vitro in lymphocytes from myeloma patients |
title_full_unstemmed | Anticancer potential of myricetin bulk and nano forms in vitro in lymphocytes from myeloma patients |
title_short | Anticancer potential of myricetin bulk and nano forms in vitro in lymphocytes from myeloma patients |
title_sort | anticancer potential of myricetin bulk and nano forms in vitro in lymphocytes from myeloma patients |
topic | Genotoxicity and Carcinogenicity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811500/ https://www.ncbi.nlm.nih.gov/pubmed/33128380 http://dx.doi.org/10.1007/s00204-020-02938-5 |
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