Gummosin, a sesquiterpene coumarin from Ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell lines
<strong><span style="font-size: medium;">Objective:</span></strong><span style="font-size: medium;"> The present study was conducted to find cytotoxic compounds from oleo-gum-resin of <em>Ferula assa-foetida</em></span><span styl...
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Mashhad University of Medical Sciences
2019-08-01
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doaj-0c77d038e1264f499e7afdd37b91cda32020-11-25T00:46:14ZengMashhad University of Medical SciencesAvicenna Journal of Phytomedicine2228-79302228-79492019-08-019544645310.22038/ajp.2019.1259812598Gummosin, a sesquiterpene coumarin from Ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell linesMilad Iranshahi0Faegheh Farhadi1Babak Paknejad2Parvin Zareian3Mehrdad Iranshahi4Masoumeh Karami5Seyed Reza Abtahi6Department of Pharmacology and Toxicology, Faculty of Medicine, AJA University of Medical Sciences, Tehran, Iran.|AJA Cancer Epidemiology Research and Treatment Center (AJA- CERTC), AJA University of Medical Sciences, Tehran, Iran.Department of Pharmacognosy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.Department of Pharmacology and Toxicology, Faculty of Medicine, AJA University of Medical Sciences, Tehran, IranDepartment of Physiology, School of Medicine, AJA University of Medical Sciences, Tehran, IranBiotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.Biochemistry Department, Faculty of Medicine, AJA University of Medical Sciences, Tehran, Iran.Department of Pharmacology and Toxicology, Faculty of Medicine, AJA University of Medical Sciences, Tehran, Iran.<strong><span style="font-size: medium;">Objective:</span></strong><span style="font-size: medium;"> The present study was conducted to find cytotoxic compounds from oleo-gum-resin of <em>Ferula assa-foetida</em></span><span style="font-size: medium;"> (asafoetida).</span><br /> <strong><span style="font-size: medium;">Materials and Methods:</span></strong><span style="font-size: medium;"> A dichloromethane extract of asafoetida was subjected to different chromatography analyses (including column chromatography, preparative thin layer chromatography and high performance liquid chromatography) to isolate its bioactive sesquiterpene coumarins. The structures of isolated compounds were elucidated through </span><sup><span style="font-size: small;">1</span></sup><span style="font-size: medium;">H-NMR spectra interpretation and comparison with those reported in the literature. To measure the cytotoxic activity of pure compounds, a non-fluorescent substrate called resazurin (alamarBlue</span><sup><span style="font-size: small;">®</span></sup><span style="font-size: medium;">)</span><span style="font-size: medium;">was used in this study. Human breast and prostate cancer cell lines (MCF-7 and PC-3, respectively) and a normal human embryonic stem cell (NIH) were treated with different concentrations (50, 25, 12.5 and 6.25 µg/mL) of pure compounds.</span><br /> <strong><span style="font-size: medium;">Results:</span></strong><span style="font-size: medium;"> In this study, 10 sesquiterpene coumarins were isolated from oleo-gum-resin of <em>F. assa-foetida</em></span><span style="font-size: medium;"> and cytotoxic activity of 6 compounds was tested against MCF-7 and PC-3 cell lines and NIH cells. Badrakemin acetate (7), ferukrinone (8) and deacetyl kellerin (10) were found for the first time in the oleo-gum-resin of </span><em><span style="font-size: medium;">F. assa-foetida</span></em><span style="font-size: medium;">. Gummosin (4) showed moderate cytotoxic activity with IC</span><sub><span style="font-size: small;">50</span></sub><span style="font-size: medium;"> values of 30 and 32.1 µg/mL against PC-3 and MCF-7 cell lines, respectively. None of the isolated compounds showed toxicity against NIH as a normal human cell line. </span><br /> <span style="font-size: medium;"><strong>Conclusion:</strong> The preferential cytotoxic activity of gummosin against cancer cell lines is reported for the first time in this study.</span>http://ajp.mums.ac.ir/article_12598_71632e9abbd2635c696c52a60bf6a6de.pdfFerula assa-foetidaApiaceaeGummosinCytotoxicityMCF-7PC-3 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Milad Iranshahi Faegheh Farhadi Babak Paknejad Parvin Zareian Mehrdad Iranshahi Masoumeh Karami Seyed Reza Abtahi |
spellingShingle |
Milad Iranshahi Faegheh Farhadi Babak Paknejad Parvin Zareian Mehrdad Iranshahi Masoumeh Karami Seyed Reza Abtahi Gummosin, a sesquiterpene coumarin from Ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell lines Avicenna Journal of Phytomedicine Ferula assa-foetida Apiaceae Gummosin Cytotoxicity MCF-7 PC-3 |
author_facet |
Milad Iranshahi Faegheh Farhadi Babak Paknejad Parvin Zareian Mehrdad Iranshahi Masoumeh Karami Seyed Reza Abtahi |
author_sort |
Milad Iranshahi |
title |
Gummosin, a sesquiterpene coumarin from Ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell lines |
title_short |
Gummosin, a sesquiterpene coumarin from Ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell lines |
title_full |
Gummosin, a sesquiterpene coumarin from Ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell lines |
title_fullStr |
Gummosin, a sesquiterpene coumarin from Ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell lines |
title_full_unstemmed |
Gummosin, a sesquiterpene coumarin from Ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell lines |
title_sort |
gummosin, a sesquiterpene coumarin from ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell lines |
publisher |
Mashhad University of Medical Sciences |
series |
Avicenna Journal of Phytomedicine |
issn |
2228-7930 2228-7949 |
publishDate |
2019-08-01 |
description |
<strong><span style="font-size: medium;">Objective:</span></strong><span style="font-size: medium;"> The present study was conducted to find cytotoxic compounds from oleo-gum-resin of <em>Ferula assa-foetida</em></span><span style="font-size: medium;"> (asafoetida).</span><br /> <strong><span style="font-size: medium;">Materials and Methods:</span></strong><span style="font-size: medium;"> A dichloromethane extract of asafoetida was subjected to different chromatography analyses (including column chromatography, preparative thin layer chromatography and high performance liquid chromatography) to isolate its bioactive sesquiterpene coumarins. The structures of isolated compounds were elucidated through </span><sup><span style="font-size: small;">1</span></sup><span style="font-size: medium;">H-NMR spectra interpretation and comparison with those reported in the literature. To measure the cytotoxic activity of pure compounds, a non-fluorescent substrate called resazurin (alamarBlue</span><sup><span style="font-size: small;">®</span></sup><span style="font-size: medium;">)</span><span style="font-size: medium;">was used in this study. Human breast and prostate cancer cell lines (MCF-7 and PC-3, respectively) and a normal human embryonic stem cell (NIH) were treated with different concentrations (50, 25, 12.5 and 6.25 µg/mL) of pure compounds.</span><br /> <strong><span style="font-size: medium;">Results:</span></strong><span style="font-size: medium;"> In this study, 10 sesquiterpene coumarins were isolated from oleo-gum-resin of <em>F. assa-foetida</em></span><span style="font-size: medium;"> and cytotoxic activity of 6 compounds was tested against MCF-7 and PC-3 cell lines and NIH cells. Badrakemin acetate (7), ferukrinone (8) and deacetyl kellerin (10) were found for the first time in the oleo-gum-resin of </span><em><span style="font-size: medium;">F. assa-foetida</span></em><span style="font-size: medium;">. Gummosin (4) showed moderate cytotoxic activity with IC</span><sub><span style="font-size: small;">50</span></sub><span style="font-size: medium;"> values of 30 and 32.1 µg/mL against PC-3 and MCF-7 cell lines, respectively. None of the isolated compounds showed toxicity against NIH as a normal human cell line. </span><br /> <span style="font-size: medium;"><strong>Conclusion:</strong> The preferential cytotoxic activity of gummosin against cancer cell lines is reported for the first time in this study.</span> |
topic |
Ferula assa-foetida Apiaceae Gummosin Cytotoxicity MCF-7 PC-3 |
url |
http://ajp.mums.ac.ir/article_12598_71632e9abbd2635c696c52a60bf6a6de.pdf |
work_keys_str_mv |
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