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Extracts from Pulsatilla patens target cancer-related signaling pathways in HeLa cells
The purpose of this study was to determine if a methanolic extract of the Pulsatilla patens (L.) Mill. can inhibit the progression of cancer through the modulation of cancer-related metabolic signaling pathways. We analyzed a panel of 13 inducible luciferase reporter gene vectors which expression is...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138020/ https://www.ncbi.nlm.nih.gov/pubmed/34017038 http://dx.doi.org/10.1038/s41598-021-90136-3 |
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author | Łaska, Grażyna Maciejewska-Turska, Magdalena Sieniawska, Elwira Świątek, Łukasz Pasco, David S. Balachandran, Premalatha |
author_facet | Łaska, Grażyna Maciejewska-Turska, Magdalena Sieniawska, Elwira Świątek, Łukasz Pasco, David S. Balachandran, Premalatha |
author_sort | Łaska, Grażyna |
collection | PubMed |
description | The purpose of this study was to determine if a methanolic extract of the Pulsatilla patens (L.) Mill. can inhibit the progression of cancer through the modulation of cancer-related metabolic signaling pathways. We analyzed a panel of 13 inducible luciferase reporter gene vectors which expression is driven by enhancer elements that bind to specific transcription factors for the evaluation of the activity of cancer signaling pathways. The root extract of P. patens exhibited strong inhibition of several signaling pathways in HeLa cells, a cervical cancer cell line, and was found to be the most potent in inhibiting the activation of Stat3, Smad, AP-1, NF-κB, MYC, Ets, Wnt and Hdghog, at a concentration of 40 µg/mL. The methanolic extracts of P. patens enhanced apoptotic death, deregulated cellular proliferation, differentiation, and progression towards the neoplastic phenotype by altering key signaling molecules required for cell cycle progression. This is the first study to report the influence of Pulsatilla species on cancer signaling pathways. Further, our detailed phytochemical analysis of the methanolic extracts of the P. patens allowed to deduce that compounds, which strongly suppressed the growth and proliferation of HeLa cancer cells were mainly triterpenoid saponins accompanied by phenolic acids. |
format | Online Article Text |
id | pubmed-8138020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81380202021-05-25 Extracts from Pulsatilla patens target cancer-related signaling pathways in HeLa cells Łaska, Grażyna Maciejewska-Turska, Magdalena Sieniawska, Elwira Świątek, Łukasz Pasco, David S. Balachandran, Premalatha Sci Rep Article The purpose of this study was to determine if a methanolic extract of the Pulsatilla patens (L.) Mill. can inhibit the progression of cancer through the modulation of cancer-related metabolic signaling pathways. We analyzed a panel of 13 inducible luciferase reporter gene vectors which expression is driven by enhancer elements that bind to specific transcription factors for the evaluation of the activity of cancer signaling pathways. The root extract of P. patens exhibited strong inhibition of several signaling pathways in HeLa cells, a cervical cancer cell line, and was found to be the most potent in inhibiting the activation of Stat3, Smad, AP-1, NF-κB, MYC, Ets, Wnt and Hdghog, at a concentration of 40 µg/mL. The methanolic extracts of P. patens enhanced apoptotic death, deregulated cellular proliferation, differentiation, and progression towards the neoplastic phenotype by altering key signaling molecules required for cell cycle progression. This is the first study to report the influence of Pulsatilla species on cancer signaling pathways. Further, our detailed phytochemical analysis of the methanolic extracts of the P. patens allowed to deduce that compounds, which strongly suppressed the growth and proliferation of HeLa cancer cells were mainly triterpenoid saponins accompanied by phenolic acids. Nature Publishing Group UK 2021-05-20 /pmc/articles/PMC8138020/ /pubmed/34017038 http://dx.doi.org/10.1038/s41598-021-90136-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Łaska, Grażyna Maciejewska-Turska, Magdalena Sieniawska, Elwira Świątek, Łukasz Pasco, David S. Balachandran, Premalatha Extracts from Pulsatilla patens target cancer-related signaling pathways in HeLa cells |
title | Extracts from Pulsatilla patens target cancer-related signaling pathways in HeLa cells |
title_full | Extracts from Pulsatilla patens target cancer-related signaling pathways in HeLa cells |
title_fullStr | Extracts from Pulsatilla patens target cancer-related signaling pathways in HeLa cells |
title_full_unstemmed | Extracts from Pulsatilla patens target cancer-related signaling pathways in HeLa cells |
title_short | Extracts from Pulsatilla patens target cancer-related signaling pathways in HeLa cells |
title_sort | extracts from pulsatilla patens target cancer-related signaling pathways in hela cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138020/ https://www.ncbi.nlm.nih.gov/pubmed/34017038 http://dx.doi.org/10.1038/s41598-021-90136-3 |
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