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Antiausterity Activity of Secondary Metabolites from the Roots of Ferula hezarlalehzarica against the PANC-1 Human Pancreatic Cancer Cell Line
[Image: see text] Human pancreatic cancer is one of the most aggressive types of cancer, with a high mortality rate. Due to the high tolerance of such cancer cells to nutrient starvation conditions, they can survive in a hypovascular tumor microenvironment. In this study, the dichloromethane extract...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society and American
Society of Pharmacognosy
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307951/ https://www.ncbi.nlm.nih.gov/pubmed/32163286 http://dx.doi.org/10.1021/acs.jnatprod.9b01109 |
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author | Alilou, Mostafa Dibwe, Dya Fita Schwaiger, Stefan Khodami, Mojtaba Troppmair, Jakob Awale, Suresh Stuppner, Hermann |
author_facet | Alilou, Mostafa Dibwe, Dya Fita Schwaiger, Stefan Khodami, Mojtaba Troppmair, Jakob Awale, Suresh Stuppner, Hermann |
author_sort | Alilou, Mostafa |
collection | PubMed |
description | [Image: see text] Human pancreatic cancer is one of the most aggressive types of cancer, with a high mortality rate. Due to the high tolerance of such cancer cells to nutrient starvation conditions, they can survive in a hypovascular tumor microenvironment. In this study, the dichloromethane extract of the roots of Ferula hezarlalehzarica showed potent preferential cytotoxic activity with a PC(50) value of 0.78 μg/mL. Phytochemical investigation of this extract led to the isolation of 18 compounds, including one new sesquiterpenoid (6) and one new monoterpenoid (18). All isolated compounds were evaluated for their preferential cytotoxicity against PANC-1 human pancreatic cancer cells by employing an antiausterity strategy. Among them, ferutinin (2) was identified as the most active compound, with a PC(50) value of 0.72 μM. In addition, the real-time effect of ferutinin (2) and compound 6 against PANC-1 cells, exposed to a nutrient-deprived medium (NDM), showed cell shrinkage, leading to cancer cell death within a short period of exposure. Compounds 2 and 6 also inhibited colony formation of PANC-1 cells. The present study indicates that the dichloromethane extract of the roots of F. hezarlalehzarica is a rich source of bioactive compounds for targeting PANC-1 cells. |
format | Online Article Text |
id | pubmed-7307951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society and American
Society of Pharmacognosy |
record_format | MEDLINE/PubMed |
spelling | pubmed-73079512020-06-23 Antiausterity Activity of Secondary Metabolites from the Roots of Ferula hezarlalehzarica against the PANC-1 Human Pancreatic Cancer Cell Line Alilou, Mostafa Dibwe, Dya Fita Schwaiger, Stefan Khodami, Mojtaba Troppmair, Jakob Awale, Suresh Stuppner, Hermann J Nat Prod [Image: see text] Human pancreatic cancer is one of the most aggressive types of cancer, with a high mortality rate. Due to the high tolerance of such cancer cells to nutrient starvation conditions, they can survive in a hypovascular tumor microenvironment. In this study, the dichloromethane extract of the roots of Ferula hezarlalehzarica showed potent preferential cytotoxic activity with a PC(50) value of 0.78 μg/mL. Phytochemical investigation of this extract led to the isolation of 18 compounds, including one new sesquiterpenoid (6) and one new monoterpenoid (18). All isolated compounds were evaluated for their preferential cytotoxicity against PANC-1 human pancreatic cancer cells by employing an antiausterity strategy. Among them, ferutinin (2) was identified as the most active compound, with a PC(50) value of 0.72 μM. In addition, the real-time effect of ferutinin (2) and compound 6 against PANC-1 cells, exposed to a nutrient-deprived medium (NDM), showed cell shrinkage, leading to cancer cell death within a short period of exposure. Compounds 2 and 6 also inhibited colony formation of PANC-1 cells. The present study indicates that the dichloromethane extract of the roots of F. hezarlalehzarica is a rich source of bioactive compounds for targeting PANC-1 cells. American Chemical Society and American Society of Pharmacognosy 2020-03-12 2020-04-24 /pmc/articles/PMC7307951/ /pubmed/32163286 http://dx.doi.org/10.1021/acs.jnatprod.9b01109 Text en Copyright © 2020 American Chemical Society and American Society of Pharmacognosy This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Alilou, Mostafa Dibwe, Dya Fita Schwaiger, Stefan Khodami, Mojtaba Troppmair, Jakob Awale, Suresh Stuppner, Hermann Antiausterity Activity of Secondary Metabolites from the Roots of Ferula hezarlalehzarica against the PANC-1 Human Pancreatic Cancer Cell Line |
title | Antiausterity Activity of Secondary Metabolites from
the Roots of Ferula hezarlalehzarica against the
PANC-1 Human Pancreatic Cancer Cell Line |
title_full | Antiausterity Activity of Secondary Metabolites from
the Roots of Ferula hezarlalehzarica against the
PANC-1 Human Pancreatic Cancer Cell Line |
title_fullStr | Antiausterity Activity of Secondary Metabolites from
the Roots of Ferula hezarlalehzarica against the
PANC-1 Human Pancreatic Cancer Cell Line |
title_full_unstemmed | Antiausterity Activity of Secondary Metabolites from
the Roots of Ferula hezarlalehzarica against the
PANC-1 Human Pancreatic Cancer Cell Line |
title_short | Antiausterity Activity of Secondary Metabolites from
the Roots of Ferula hezarlalehzarica against the
PANC-1 Human Pancreatic Cancer Cell Line |
title_sort | antiausterity activity of secondary metabolites from
the roots of ferula hezarlalehzarica against the
panc-1 human pancreatic cancer cell line |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307951/ https://www.ncbi.nlm.nih.gov/pubmed/32163286 http://dx.doi.org/10.1021/acs.jnatprod.9b01109 |
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