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Anti‐angiogenic effects of the blue‐green alga Arthrospira platensis on pancreatic cancer

Arthrospira platensis, a blue‐green alga, is a popular nutraceutical substance having potent antioxidant properties with potential anti‐carcinogenic activities. The aim of our study was to assess the possible anti‐angiogenic effects of A platensis in an experimental model of pancreatic cancer. The e...

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Autores principales: Marková, Ivana, Koníčková, Renata, Vaňková, Kateřina, Leníček, Martin, Kolář, Michal, Strnad, Hynek, Hradilová, Miluše, Šáchová, Jana, Rasl, Jan, Klímová, Zuzana, Vomastek, Tomáš, Němečková, Ivana, Nachtigal, Petr, Vítek, Libor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028863/
https://www.ncbi.nlm.nih.gov/pubmed/31957261
http://dx.doi.org/10.1111/jcmm.14922
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author Marková, Ivana
Koníčková, Renata
Vaňková, Kateřina
Leníček, Martin
Kolář, Michal
Strnad, Hynek
Hradilová, Miluše
Šáchová, Jana
Rasl, Jan
Klímová, Zuzana
Vomastek, Tomáš
Němečková, Ivana
Nachtigal, Petr
Vítek, Libor
author_facet Marková, Ivana
Koníčková, Renata
Vaňková, Kateřina
Leníček, Martin
Kolář, Michal
Strnad, Hynek
Hradilová, Miluše
Šáchová, Jana
Rasl, Jan
Klímová, Zuzana
Vomastek, Tomáš
Němečková, Ivana
Nachtigal, Petr
Vítek, Libor
author_sort Marková, Ivana
collection PubMed
description Arthrospira platensis, a blue‐green alga, is a popular nutraceutical substance having potent antioxidant properties with potential anti‐carcinogenic activities. The aim of our study was to assess the possible anti‐angiogenic effects of A platensis in an experimental model of pancreatic cancer. The effects of an A platensis extract were investigated on human pancreatic cancer cells (PA‐TU‐8902) and immortalized endothelial‐like cells (Ea.hy926). PA‐TU‐8902 pancreatic tumours xenografted to athymic mice were also examined. In vitro migration and invasiveness assays were performed on the tested cells. Multiple angiogenic factors and signalling pathways were analysed in the epithelial, endothelial and cancer cells, and tumour tissue. The A platensis extract exerted inhibitory effects on both migration and invasion of pancreatic cancer as well as endothelial‐like cells. Tumours of mice treated with A platensis exhibited much lesser degrees of vascularization as measured by CD31 immunostaining (P = .004). Surprisingly, the VEGF‐A mRNA and protein expressions were up‐regulated in pancreatic cancer cells. A platensis inhibited ERK activation upstream of Raf and suppressed the expression of ERK‐regulated proteins. Treatment of pancreatic cancer with A platensis was associated with suppressive effects on migration and invasiveness with various anti‐angiogenic features, which might account for the anticancer effects of this blue‐green alga.
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spelling pubmed-70288632020-02-19 Anti‐angiogenic effects of the blue‐green alga Arthrospira platensis on pancreatic cancer Marková, Ivana Koníčková, Renata Vaňková, Kateřina Leníček, Martin Kolář, Michal Strnad, Hynek Hradilová, Miluše Šáchová, Jana Rasl, Jan Klímová, Zuzana Vomastek, Tomáš Němečková, Ivana Nachtigal, Petr Vítek, Libor J Cell Mol Med Original Articles Arthrospira platensis, a blue‐green alga, is a popular nutraceutical substance having potent antioxidant properties with potential anti‐carcinogenic activities. The aim of our study was to assess the possible anti‐angiogenic effects of A platensis in an experimental model of pancreatic cancer. The effects of an A platensis extract were investigated on human pancreatic cancer cells (PA‐TU‐8902) and immortalized endothelial‐like cells (Ea.hy926). PA‐TU‐8902 pancreatic tumours xenografted to athymic mice were also examined. In vitro migration and invasiveness assays were performed on the tested cells. Multiple angiogenic factors and signalling pathways were analysed in the epithelial, endothelial and cancer cells, and tumour tissue. The A platensis extract exerted inhibitory effects on both migration and invasion of pancreatic cancer as well as endothelial‐like cells. Tumours of mice treated with A platensis exhibited much lesser degrees of vascularization as measured by CD31 immunostaining (P = .004). Surprisingly, the VEGF‐A mRNA and protein expressions were up‐regulated in pancreatic cancer cells. A platensis inhibited ERK activation upstream of Raf and suppressed the expression of ERK‐regulated proteins. Treatment of pancreatic cancer with A platensis was associated with suppressive effects on migration and invasiveness with various anti‐angiogenic features, which might account for the anticancer effects of this blue‐green alga. John Wiley and Sons Inc. 2020-01-19 2020-02 /pmc/articles/PMC7028863/ /pubmed/31957261 http://dx.doi.org/10.1111/jcmm.14922 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Marková, Ivana
Koníčková, Renata
Vaňková, Kateřina
Leníček, Martin
Kolář, Michal
Strnad, Hynek
Hradilová, Miluše
Šáchová, Jana
Rasl, Jan
Klímová, Zuzana
Vomastek, Tomáš
Němečková, Ivana
Nachtigal, Petr
Vítek, Libor
Anti‐angiogenic effects of the blue‐green alga Arthrospira platensis on pancreatic cancer
title Anti‐angiogenic effects of the blue‐green alga Arthrospira platensis on pancreatic cancer
title_full Anti‐angiogenic effects of the blue‐green alga Arthrospira platensis on pancreatic cancer
title_fullStr Anti‐angiogenic effects of the blue‐green alga Arthrospira platensis on pancreatic cancer
title_full_unstemmed Anti‐angiogenic effects of the blue‐green alga Arthrospira platensis on pancreatic cancer
title_short Anti‐angiogenic effects of the blue‐green alga Arthrospira platensis on pancreatic cancer
title_sort anti‐angiogenic effects of the blue‐green alga arthrospira platensis on pancreatic cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028863/
https://www.ncbi.nlm.nih.gov/pubmed/31957261
http://dx.doi.org/10.1111/jcmm.14922
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