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Potential Effect of Pseudevernia furfuracea (L.) Zopf Extract and Metabolite Physodic Acid on Tumour Microenvironment Modulation in MCF-10A Cells

Lichens comprise a number of unique secondary metabolites with remarkable biological activities and have become an interesting research topic for cancer therapy. However, only a few of these metabolites have been assessed for their effectiveness against various in vitro models. Therefore, the aim of...

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Autores principales: Petrova, Klaudia, Kello, Martin, Kuruc, Tomas, Backorova, Miriam, Petrovova, Eva, Vilkova, Maria, Goga, Michal, Rucova, Dajana, Backor, Martin, Mojzis, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000760/
https://www.ncbi.nlm.nih.gov/pubmed/33809098
http://dx.doi.org/10.3390/biom11030420
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author Petrova, Klaudia
Kello, Martin
Kuruc, Tomas
Backorova, Miriam
Petrovova, Eva
Vilkova, Maria
Goga, Michal
Rucova, Dajana
Backor, Martin
Mojzis, Jan
author_facet Petrova, Klaudia
Kello, Martin
Kuruc, Tomas
Backorova, Miriam
Petrovova, Eva
Vilkova, Maria
Goga, Michal
Rucova, Dajana
Backor, Martin
Mojzis, Jan
author_sort Petrova, Klaudia
collection PubMed
description Lichens comprise a number of unique secondary metabolites with remarkable biological activities and have become an interesting research topic for cancer therapy. However, only a few of these metabolites have been assessed for their effectiveness against various in vitro models. Therefore, the aim of the present study was to assess the effect of extract Pseudevernia furfuracea (L.) Zopf (PSE) and its metabolite physodic acid (Phy) on tumour microenvironment (TME) modulation, focusing on epithelial–mesenchymal transition (EMT), cancer-associated fibroblasts (CAFs) transformation and angiogenesis. Here, we demonstrate, by using flow cytometry, Western blot and immunofluorescence microscopy, that tested compounds inhibited the EMT process in MCF-10A breast cells through decreasing the level of different mesenchymal markers in a time- and dose-dependent manner. By the same mechanisms, PSE and Phy suppressed the function of Transforming growth factor beta (TGF-β)-stimulated fibroblasts. Moreover, PSE and Phy resulted in a decreasing level of the TGF-β canonical pathway Smad2/3, which is essential for tumour growth. Furthermore, PSE and Phy inhibited angiogenesis ex ovo in a quail embryo chorioallantoic model, which indicates their potential anti-angiogenic activity. These results also provided the first evidence of the modulation of TME by these substances.
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spelling pubmed-80007602021-03-28 Potential Effect of Pseudevernia furfuracea (L.) Zopf Extract and Metabolite Physodic Acid on Tumour Microenvironment Modulation in MCF-10A Cells Petrova, Klaudia Kello, Martin Kuruc, Tomas Backorova, Miriam Petrovova, Eva Vilkova, Maria Goga, Michal Rucova, Dajana Backor, Martin Mojzis, Jan Biomolecules Article Lichens comprise a number of unique secondary metabolites with remarkable biological activities and have become an interesting research topic for cancer therapy. However, only a few of these metabolites have been assessed for their effectiveness against various in vitro models. Therefore, the aim of the present study was to assess the effect of extract Pseudevernia furfuracea (L.) Zopf (PSE) and its metabolite physodic acid (Phy) on tumour microenvironment (TME) modulation, focusing on epithelial–mesenchymal transition (EMT), cancer-associated fibroblasts (CAFs) transformation and angiogenesis. Here, we demonstrate, by using flow cytometry, Western blot and immunofluorescence microscopy, that tested compounds inhibited the EMT process in MCF-10A breast cells through decreasing the level of different mesenchymal markers in a time- and dose-dependent manner. By the same mechanisms, PSE and Phy suppressed the function of Transforming growth factor beta (TGF-β)-stimulated fibroblasts. Moreover, PSE and Phy resulted in a decreasing level of the TGF-β canonical pathway Smad2/3, which is essential for tumour growth. Furthermore, PSE and Phy inhibited angiogenesis ex ovo in a quail embryo chorioallantoic model, which indicates their potential anti-angiogenic activity. These results also provided the first evidence of the modulation of TME by these substances. MDPI 2021-03-12 /pmc/articles/PMC8000760/ /pubmed/33809098 http://dx.doi.org/10.3390/biom11030420 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Petrova, Klaudia
Kello, Martin
Kuruc, Tomas
Backorova, Miriam
Petrovova, Eva
Vilkova, Maria
Goga, Michal
Rucova, Dajana
Backor, Martin
Mojzis, Jan
Potential Effect of Pseudevernia furfuracea (L.) Zopf Extract and Metabolite Physodic Acid on Tumour Microenvironment Modulation in MCF-10A Cells
title Potential Effect of Pseudevernia furfuracea (L.) Zopf Extract and Metabolite Physodic Acid on Tumour Microenvironment Modulation in MCF-10A Cells
title_full Potential Effect of Pseudevernia furfuracea (L.) Zopf Extract and Metabolite Physodic Acid on Tumour Microenvironment Modulation in MCF-10A Cells
title_fullStr Potential Effect of Pseudevernia furfuracea (L.) Zopf Extract and Metabolite Physodic Acid on Tumour Microenvironment Modulation in MCF-10A Cells
title_full_unstemmed Potential Effect of Pseudevernia furfuracea (L.) Zopf Extract and Metabolite Physodic Acid on Tumour Microenvironment Modulation in MCF-10A Cells
title_short Potential Effect of Pseudevernia furfuracea (L.) Zopf Extract and Metabolite Physodic Acid on Tumour Microenvironment Modulation in MCF-10A Cells
title_sort potential effect of pseudevernia furfuracea (l.) zopf extract and metabolite physodic acid on tumour microenvironment modulation in mcf-10a cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000760/
https://www.ncbi.nlm.nih.gov/pubmed/33809098
http://dx.doi.org/10.3390/biom11030420
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