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Selectivity of Pinus sylvestris extract and essential oil to estrogen-insensitive breast cancer cells Pinus sylvestris against cancer cells

BACKGROUND: So far, the anticancer action of pine tree extracts has mainly been shown for the species distributed widely around the Asian countries. OBJECTIVE: Therefore, this study was performed to examine the potential cytotoxicity of Scots pine (Pinus sylvestris L.) native also to the European re...

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Autores principales: Hoai, Nguyen Thi, Duc, Ho Viet, Thao, Do Thi, Orav, Anne, Raal, Ain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4653339/
https://www.ncbi.nlm.nih.gov/pubmed/26664017
http://dx.doi.org/10.4103/0973-1296.166052
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author Hoai, Nguyen Thi
Duc, Ho Viet
Thao, Do Thi
Orav, Anne
Raal, Ain
author_facet Hoai, Nguyen Thi
Duc, Ho Viet
Thao, Do Thi
Orav, Anne
Raal, Ain
author_sort Hoai, Nguyen Thi
collection PubMed
description BACKGROUND: So far, the anticancer action of pine tree extracts has mainly been shown for the species distributed widely around the Asian countries. OBJECTIVE: Therefore, this study was performed to examine the potential cytotoxicity of Scots pine (Pinus sylvestris L.) native also to the European region and growing widely in Estonia. MATERIALS AND METHODS: The cytotoxic activity of methanol extract and essential oil of Scots pine needles was determined by sulforhodamine B assay in different human cancer cell lines. RESULTS: This needle extract was found to suppress the viability of several human cancer cell lines showing some selectivity to estrogen receptor negative breast cancer cells, MDA-MB-231(half maximal inhibitory concentration [IC(50)] 35 μg/ml) in comparison with estrogen receptor-positive breast cancer cells, MCF-7 (IC(50) 86 μg/ml). It is the strongest cytotoxic effect at all measured, thus far for the needles and leaves extracts derived from various pine species, and is also the first study comparing the anticancer effects of pine tree extracts on molecularly different human breast cancer cells. The essential oil showed the stronger cytotoxic effect to both negative and positive breast cancer cell lines (both IC(50) 29 μg/ml) than pine extract (IC(50) 42 and 80 μg/ml, respectively). CONCLUSION: The data from this report indicate that Scots pine needles extract and essential oil exhibits some potential as chemopreventive or chemotherapeutic agent for mammary tumors unresponsive to endocrine treatment.
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spelling pubmed-46533392015-12-09 Selectivity of Pinus sylvestris extract and essential oil to estrogen-insensitive breast cancer cells Pinus sylvestris against cancer cells Hoai, Nguyen Thi Duc, Ho Viet Thao, Do Thi Orav, Anne Raal, Ain Pharmacogn Mag Original Article BACKGROUND: So far, the anticancer action of pine tree extracts has mainly been shown for the species distributed widely around the Asian countries. OBJECTIVE: Therefore, this study was performed to examine the potential cytotoxicity of Scots pine (Pinus sylvestris L.) native also to the European region and growing widely in Estonia. MATERIALS AND METHODS: The cytotoxic activity of methanol extract and essential oil of Scots pine needles was determined by sulforhodamine B assay in different human cancer cell lines. RESULTS: This needle extract was found to suppress the viability of several human cancer cell lines showing some selectivity to estrogen receptor negative breast cancer cells, MDA-MB-231(half maximal inhibitory concentration [IC(50)] 35 μg/ml) in comparison with estrogen receptor-positive breast cancer cells, MCF-7 (IC(50) 86 μg/ml). It is the strongest cytotoxic effect at all measured, thus far for the needles and leaves extracts derived from various pine species, and is also the first study comparing the anticancer effects of pine tree extracts on molecularly different human breast cancer cells. The essential oil showed the stronger cytotoxic effect to both negative and positive breast cancer cell lines (both IC(50) 29 μg/ml) than pine extract (IC(50) 42 and 80 μg/ml, respectively). CONCLUSION: The data from this report indicate that Scots pine needles extract and essential oil exhibits some potential as chemopreventive or chemotherapeutic agent for mammary tumors unresponsive to endocrine treatment. Medknow Publications & Media Pvt Ltd 2015-10 /pmc/articles/PMC4653339/ /pubmed/26664017 http://dx.doi.org/10.4103/0973-1296.166052 Text en Copyright: © Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Hoai, Nguyen Thi
Duc, Ho Viet
Thao, Do Thi
Orav, Anne
Raal, Ain
Selectivity of Pinus sylvestris extract and essential oil to estrogen-insensitive breast cancer cells Pinus sylvestris against cancer cells
title Selectivity of Pinus sylvestris extract and essential oil to estrogen-insensitive breast cancer cells Pinus sylvestris against cancer cells
title_full Selectivity of Pinus sylvestris extract and essential oil to estrogen-insensitive breast cancer cells Pinus sylvestris against cancer cells
title_fullStr Selectivity of Pinus sylvestris extract and essential oil to estrogen-insensitive breast cancer cells Pinus sylvestris against cancer cells
title_full_unstemmed Selectivity of Pinus sylvestris extract and essential oil to estrogen-insensitive breast cancer cells Pinus sylvestris against cancer cells
title_short Selectivity of Pinus sylvestris extract and essential oil to estrogen-insensitive breast cancer cells Pinus sylvestris against cancer cells
title_sort selectivity of pinus sylvestris extract and essential oil to estrogen-insensitive breast cancer cells pinus sylvestris against cancer cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4653339/
https://www.ncbi.nlm.nih.gov/pubmed/26664017
http://dx.doi.org/10.4103/0973-1296.166052
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