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Candida albicans Beta-Glucan Induce Anti- Cancer Activity of Mesenchymal Stem Cells against Lung Cancer Cell Line: An In-Vitro Experimental Study

OBJECTIVE: β-glucan, glucopyranosyl polymers of fungi cell wall, represent an immune stimulating effects with potential anti-cancer activity. Mesenchymal stem cells (MSC) have immunomodulating properties in cancer microenvironment. The aim of this study was to investigate the anti-cancer effect of C...

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Autores principales: Peymaeei, Fatemeh, Sadeghi, Fatemeh, Safari, Elahe, Khorrami, Samaneh, Falahati, Mehraban, Roudbar Mohammadi, Shahla, Roudbary, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437339/
https://www.ncbi.nlm.nih.gov/pubmed/32212815
http://dx.doi.org/10.31557/APJCP.2020.21.3.837
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author Peymaeei, Fatemeh
Sadeghi, Fatemeh
Safari, Elahe
Khorrami, Samaneh
Falahati, Mehraban
Roudbar Mohammadi, Shahla
Roudbary, Maryam
author_facet Peymaeei, Fatemeh
Sadeghi, Fatemeh
Safari, Elahe
Khorrami, Samaneh
Falahati, Mehraban
Roudbar Mohammadi, Shahla
Roudbary, Maryam
author_sort Peymaeei, Fatemeh
collection PubMed
description OBJECTIVE: β-glucan, glucopyranosyl polymers of fungi cell wall, represent an immune stimulating effects with potential anti-cancer activity. Mesenchymal stem cells (MSC) have immunomodulating properties in cancer microenvironment. The aim of this study was to investigate the anti-cancer effect of Candida albicans (C. albicans) beta-glucan on MSCs supernatant for apoptosis assay of lung cancer cells in vitro. METHODS: Beta-glucan was extracted from cell wall of C.albicans. MSC isolated from adipose tissue of patients and confirmed using specific surface markers expression which examined by flow cytometry. MSCs treated with various concentrations of β-glucans for 48 hours. Cytotoxic effect of β-glucans was evaluated using MTT assay. MSC and lung cancer line cocultured and treated with β-glucans and apoptosis assay was done by flow cytometry. RESULTS: Cytotoxicity findings showed a significant decrease in MSC viability during 48h, however it was dose-dependent (P<0.05). According to the obtained findings, supernatant of mesenchymal stem cells treated with β-glucans increased cancer cells apoptosis (P<0.05). CONCLUSION: Beta glucan may highlight a potential and novel promising candidate in future strategies to cause apoptosis of cancer cells and consider as therapeutic agent against tumor growth as well. Definitely, more in vitro and in vivo studies are required to understand its functions.
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spelling pubmed-74373392020-09-02 Candida albicans Beta-Glucan Induce Anti- Cancer Activity of Mesenchymal Stem Cells against Lung Cancer Cell Line: An In-Vitro Experimental Study Peymaeei, Fatemeh Sadeghi, Fatemeh Safari, Elahe Khorrami, Samaneh Falahati, Mehraban Roudbar Mohammadi, Shahla Roudbary, Maryam Asian Pac J Cancer Prev Research Article OBJECTIVE: β-glucan, glucopyranosyl polymers of fungi cell wall, represent an immune stimulating effects with potential anti-cancer activity. Mesenchymal stem cells (MSC) have immunomodulating properties in cancer microenvironment. The aim of this study was to investigate the anti-cancer effect of Candida albicans (C. albicans) beta-glucan on MSCs supernatant for apoptosis assay of lung cancer cells in vitro. METHODS: Beta-glucan was extracted from cell wall of C.albicans. MSC isolated from adipose tissue of patients and confirmed using specific surface markers expression which examined by flow cytometry. MSCs treated with various concentrations of β-glucans for 48 hours. Cytotoxic effect of β-glucans was evaluated using MTT assay. MSC and lung cancer line cocultured and treated with β-glucans and apoptosis assay was done by flow cytometry. RESULTS: Cytotoxicity findings showed a significant decrease in MSC viability during 48h, however it was dose-dependent (P<0.05). According to the obtained findings, supernatant of mesenchymal stem cells treated with β-glucans increased cancer cells apoptosis (P<0.05). CONCLUSION: Beta glucan may highlight a potential and novel promising candidate in future strategies to cause apoptosis of cancer cells and consider as therapeutic agent against tumor growth as well. Definitely, more in vitro and in vivo studies are required to understand its functions. West Asia Organization for Cancer Prevention 2020-03 /pmc/articles/PMC7437339/ /pubmed/32212815 http://dx.doi.org/10.31557/APJCP.2020.21.3.837 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Peymaeei, Fatemeh
Sadeghi, Fatemeh
Safari, Elahe
Khorrami, Samaneh
Falahati, Mehraban
Roudbar Mohammadi, Shahla
Roudbary, Maryam
Candida albicans Beta-Glucan Induce Anti- Cancer Activity of Mesenchymal Stem Cells against Lung Cancer Cell Line: An In-Vitro Experimental Study
title Candida albicans Beta-Glucan Induce Anti- Cancer Activity of Mesenchymal Stem Cells against Lung Cancer Cell Line: An In-Vitro Experimental Study
title_full Candida albicans Beta-Glucan Induce Anti- Cancer Activity of Mesenchymal Stem Cells against Lung Cancer Cell Line: An In-Vitro Experimental Study
title_fullStr Candida albicans Beta-Glucan Induce Anti- Cancer Activity of Mesenchymal Stem Cells against Lung Cancer Cell Line: An In-Vitro Experimental Study
title_full_unstemmed Candida albicans Beta-Glucan Induce Anti- Cancer Activity of Mesenchymal Stem Cells against Lung Cancer Cell Line: An In-Vitro Experimental Study
title_short Candida albicans Beta-Glucan Induce Anti- Cancer Activity of Mesenchymal Stem Cells against Lung Cancer Cell Line: An In-Vitro Experimental Study
title_sort candida albicans beta-glucan induce anti- cancer activity of mesenchymal stem cells against lung cancer cell line: an in-vitro experimental study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437339/
https://www.ncbi.nlm.nih.gov/pubmed/32212815
http://dx.doi.org/10.31557/APJCP.2020.21.3.837
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