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Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line

BACKGROUND: Breast cancer is the most common cancer in the Arab world and it ranked first among Saudi females. Doxorubicin (DOX), an anthracycline antibiotic is one of the most effective anticancer agents used to treat breast cancer. chronic cardiotoxicity is a major limiting factor of the use of do...

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Autores principales: Osman, Abdel-Moneim M, Bayoumi, Hadeel M, Al-Harthi, Sameer E, Damanhouri, Zoheir A, ElShal, Mohamed F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537590/
https://www.ncbi.nlm.nih.gov/pubmed/23153194
http://dx.doi.org/10.1186/1475-2867-12-47
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author Osman, Abdel-Moneim M
Bayoumi, Hadeel M
Al-Harthi, Sameer E
Damanhouri, Zoheir A
ElShal, Mohamed F
author_facet Osman, Abdel-Moneim M
Bayoumi, Hadeel M
Al-Harthi, Sameer E
Damanhouri, Zoheir A
ElShal, Mohamed F
author_sort Osman, Abdel-Moneim M
collection PubMed
description BACKGROUND: Breast cancer is the most common cancer in the Arab world and it ranked first among Saudi females. Doxorubicin (DOX), an anthracycline antibiotic is one of the most effective anticancer agents used to treat breast cancer. chronic cardiotoxicity is a major limiting factor of the use of doxorubicin. Therefore, our study was designed to assess the role of a natural product resveratrol (RSVL) on sensitization of human breast cancer cells (MCF-7) to the action of DOX in an attempt to minimize doxorubicin effective dose and thereby its side effects. METHODS: Human breast cancer cell line MCF-7, was used in this study. Cytotoxic activity of DOX was determined using (sulforhodamine) SRB method. Apoptotic cells were quantified after treatment by annexin V-FITC- propidium iodide (PI) double staining using flow-cytometer. Cell cycle disturbance and doxorubicin uptake were determined after RSVL or DOX treatment. RESULTS: Treatment of MCF-7 cells with 15 μg/ml RSVL either simultaneously or 24 h before DOX increased the cytotoxicity of DOX, with IC50 were 0.056 and 0.035 μg/ml, respectively compared to DOX alone IC50 (0.417 μg/ml). Moreover, flow cytometric analysis of the MCF-7 cells treated simultaneously with DOX (0.5 μg/ml) and RSVL showed enhanced arrest of the cells in G(0) (80%). On the other hand, when RSVL is given 24 h before DOX although there was more increased in the cytotoxic effect of DOX against the growth of the cells, however, there was decreased in percentage arrest of cells in G(0), less inhibition of DOX-induced apoptosis and reduced DOX cellular uptake into the cells. CONCLUSION: RSVL treatment increased the cytotoxic activity of DOX against the growth of human breast cancer cells when given either simultaneously or 24 h before DOX.
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spelling pubmed-35375902013-01-10 Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line Osman, Abdel-Moneim M Bayoumi, Hadeel M Al-Harthi, Sameer E Damanhouri, Zoheir A ElShal, Mohamed F Cancer Cell Int Primary Research BACKGROUND: Breast cancer is the most common cancer in the Arab world and it ranked first among Saudi females. Doxorubicin (DOX), an anthracycline antibiotic is one of the most effective anticancer agents used to treat breast cancer. chronic cardiotoxicity is a major limiting factor of the use of doxorubicin. Therefore, our study was designed to assess the role of a natural product resveratrol (RSVL) on sensitization of human breast cancer cells (MCF-7) to the action of DOX in an attempt to minimize doxorubicin effective dose and thereby its side effects. METHODS: Human breast cancer cell line MCF-7, was used in this study. Cytotoxic activity of DOX was determined using (sulforhodamine) SRB method. Apoptotic cells were quantified after treatment by annexin V-FITC- propidium iodide (PI) double staining using flow-cytometer. Cell cycle disturbance and doxorubicin uptake were determined after RSVL or DOX treatment. RESULTS: Treatment of MCF-7 cells with 15 μg/ml RSVL either simultaneously or 24 h before DOX increased the cytotoxicity of DOX, with IC50 were 0.056 and 0.035 μg/ml, respectively compared to DOX alone IC50 (0.417 μg/ml). Moreover, flow cytometric analysis of the MCF-7 cells treated simultaneously with DOX (0.5 μg/ml) and RSVL showed enhanced arrest of the cells in G(0) (80%). On the other hand, when RSVL is given 24 h before DOX although there was more increased in the cytotoxic effect of DOX against the growth of the cells, however, there was decreased in percentage arrest of cells in G(0), less inhibition of DOX-induced apoptosis and reduced DOX cellular uptake into the cells. CONCLUSION: RSVL treatment increased the cytotoxic activity of DOX against the growth of human breast cancer cells when given either simultaneously or 24 h before DOX. BioMed Central 2012-11-16 /pmc/articles/PMC3537590/ /pubmed/23153194 http://dx.doi.org/10.1186/1475-2867-12-47 Text en Copyright ©2012 Osman et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Primary Research
Osman, Abdel-Moneim M
Bayoumi, Hadeel M
Al-Harthi, Sameer E
Damanhouri, Zoheir A
ElShal, Mohamed F
Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line
title Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line
title_full Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line
title_fullStr Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line
title_full_unstemmed Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line
title_short Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line
title_sort modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537590/
https://www.ncbi.nlm.nih.gov/pubmed/23153194
http://dx.doi.org/10.1186/1475-2867-12-47
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