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The effect of piperlongumine on endothelial and lung adenocarcinoma cells with regulated expression of profilin-1
PURPOSE: The aim of the study was to evaluate the effect of piperlongumine (2 and 4 µM) on endothelial EA.hy926 and lung adenocarcinoma A549 cells with regulated expression of profilin-1 (PFN1). MATERIAL AND METHODS: The cytotoxicity of alkaloid was evaluated by MTT assay, while cell death was asses...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255113/ https://www.ncbi.nlm.nih.gov/pubmed/30538497 http://dx.doi.org/10.2147/OTT.S183191 |
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author | Gagat, Maciej Hałas-Wiśniewska, Marta Zielińska, Wioletta Izdebska, Magdalena Grzanka, Dariusz Grzanka, Alina |
author_facet | Gagat, Maciej Hałas-Wiśniewska, Marta Zielińska, Wioletta Izdebska, Magdalena Grzanka, Dariusz Grzanka, Alina |
author_sort | Gagat, Maciej |
collection | PubMed |
description | PURPOSE: The aim of the study was to evaluate the effect of piperlongumine (2 and 4 µM) on endothelial EA.hy926 and lung adenocarcinoma A549 cells with regulated expression of profilin-1 (PFN1). MATERIAL AND METHODS: The cytotoxicity of alkaloid was evaluated by MTT assay, while cell death was assessed using double staining with annexin V and propidium iodide. Subsequently, the level of PFN1 1) upregulation in EA.hy926 endothelial cells and 2) downregulation in A549 lung adenocarcinoma cells. The next step was the analysis of the effect of PFN1 manipulation on cytoskeletal proteins. RESULTS: The results showed that piperlongumine may inhibit proliferation of EA.hy926 and A549 cell lines and also induce cell death in a dose-dependent manner. Furthermore, endothelial cells with PFN1 overexpression showed lower sensitivity to alkaloid and strengthening of cell–cell interactions. In the case of A549 cells, loss of PFN1 expression resulted in a lower percentage of early apoptotic cells, reorganization of F-actin and vimentin network, and reduction of migratory potential. CONCLUSION: We suggest that upregulation of PFN1 in endothelial cell line may stabilize the cell junctions. In turn, PFN1 downregulation in A549 cells probably suppresses cell migration and sensitizes cells to anticancer agents. |
format | Online Article Text |
id | pubmed-6255113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62551132018-12-11 The effect of piperlongumine on endothelial and lung adenocarcinoma cells with regulated expression of profilin-1 Gagat, Maciej Hałas-Wiśniewska, Marta Zielińska, Wioletta Izdebska, Magdalena Grzanka, Dariusz Grzanka, Alina Onco Targets Ther Original Research PURPOSE: The aim of the study was to evaluate the effect of piperlongumine (2 and 4 µM) on endothelial EA.hy926 and lung adenocarcinoma A549 cells with regulated expression of profilin-1 (PFN1). MATERIAL AND METHODS: The cytotoxicity of alkaloid was evaluated by MTT assay, while cell death was assessed using double staining with annexin V and propidium iodide. Subsequently, the level of PFN1 1) upregulation in EA.hy926 endothelial cells and 2) downregulation in A549 lung adenocarcinoma cells. The next step was the analysis of the effect of PFN1 manipulation on cytoskeletal proteins. RESULTS: The results showed that piperlongumine may inhibit proliferation of EA.hy926 and A549 cell lines and also induce cell death in a dose-dependent manner. Furthermore, endothelial cells with PFN1 overexpression showed lower sensitivity to alkaloid and strengthening of cell–cell interactions. In the case of A549 cells, loss of PFN1 expression resulted in a lower percentage of early apoptotic cells, reorganization of F-actin and vimentin network, and reduction of migratory potential. CONCLUSION: We suggest that upregulation of PFN1 in endothelial cell line may stabilize the cell junctions. In turn, PFN1 downregulation in A549 cells probably suppresses cell migration and sensitizes cells to anticancer agents. Dove Medical Press 2018-11-22 /pmc/articles/PMC6255113/ /pubmed/30538497 http://dx.doi.org/10.2147/OTT.S183191 Text en © 2018 Gagat et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Gagat, Maciej Hałas-Wiśniewska, Marta Zielińska, Wioletta Izdebska, Magdalena Grzanka, Dariusz Grzanka, Alina The effect of piperlongumine on endothelial and lung adenocarcinoma cells with regulated expression of profilin-1 |
title | The effect of piperlongumine on endothelial and lung adenocarcinoma cells with regulated expression of profilin-1 |
title_full | The effect of piperlongumine on endothelial and lung adenocarcinoma cells with regulated expression of profilin-1 |
title_fullStr | The effect of piperlongumine on endothelial and lung adenocarcinoma cells with regulated expression of profilin-1 |
title_full_unstemmed | The effect of piperlongumine on endothelial and lung adenocarcinoma cells with regulated expression of profilin-1 |
title_short | The effect of piperlongumine on endothelial and lung adenocarcinoma cells with regulated expression of profilin-1 |
title_sort | effect of piperlongumine on endothelial and lung adenocarcinoma cells with regulated expression of profilin-1 |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255113/ https://www.ncbi.nlm.nih.gov/pubmed/30538497 http://dx.doi.org/10.2147/OTT.S183191 |
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