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Anticancer potentiality of lignan rich fraction of six Flaxseed cultivars

The objective of our study is to highlight the therapeutic effect and mechanism of action by which purified Flaxseed hydrolysate (PFH) which is a lignan rich fraction exerts its anticancer activity on a human breast cancer cell line (T47D) and in mice bearing tumor. HPLC analysis of PFH of six flaxs...

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Autores principales: Ezzat, Shahira M., Shouman, Samia A., Elkhoely, Abeer, Attia, Yasmin M., Elsesy, Mohamed S., El Senousy, Amira S., Choucry, Mouchira A., El Gayed, Sabah H., El Sayed, Abeer A., Sattar, Essam Abdel, El Tanbouly, Nebal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764973/
https://www.ncbi.nlm.nih.gov/pubmed/29323210
http://dx.doi.org/10.1038/s41598-017-18944-0
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author Ezzat, Shahira M.
Shouman, Samia A.
Elkhoely, Abeer
Attia, Yasmin M.
Elsesy, Mohamed S.
El Senousy, Amira S.
Choucry, Mouchira A.
El Gayed, Sabah H.
El Sayed, Abeer A.
Sattar, Essam Abdel
El Tanbouly, Nebal
author_facet Ezzat, Shahira M.
Shouman, Samia A.
Elkhoely, Abeer
Attia, Yasmin M.
Elsesy, Mohamed S.
El Senousy, Amira S.
Choucry, Mouchira A.
El Gayed, Sabah H.
El Sayed, Abeer A.
Sattar, Essam Abdel
El Tanbouly, Nebal
author_sort Ezzat, Shahira M.
collection PubMed
description The objective of our study is to highlight the therapeutic effect and mechanism of action by which purified Flaxseed hydrolysate (PFH) which is a lignan rich fraction exerts its anticancer activity on a human breast cancer cell line (T47D) and in mice bearing tumor. HPLC analysis of PFH of six flaxseed cultivars had shown that PFH of the cultivar Giza 9 (PFH-G9) contains the highest concentration of SDG (81.64 mg/g). The in vitro cytotoxic potentiality of PFH’s of six flaxseed cultivars was screened against a panel of human cancer cell lines. PFH -G9 showed the most significant cytotoxic activity against ER-receptor positive breast cell lines MCF7 and T47D with IC(50) 13.8 and 15.8 µg/ml, respectively. Moreover, PFH-G9 reduced the expression of the metastasis marker, 1-α, metalloproteinases and vascular endothelial growth factor (VEGF), one of the most potent stimulators of angiogenesis, while it increased the caspase-3 dependent apoptosis. Our study also showed that dietary intake of 10% of Giza 9 Flaxseeds (FS), fixed oil (FSO) or Flax meal (FSM) twice daily for 3 weeks in mice-bearing solid Ehrlich ascites carcinoma (EAC) resulted in reducing the tumor volume, the expression of estrogen, insulin growth factor, progesterone, VEGF and MMP-2, but enhanced expression of caspase-3.
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spelling pubmed-57649732018-01-17 Anticancer potentiality of lignan rich fraction of six Flaxseed cultivars Ezzat, Shahira M. Shouman, Samia A. Elkhoely, Abeer Attia, Yasmin M. Elsesy, Mohamed S. El Senousy, Amira S. Choucry, Mouchira A. El Gayed, Sabah H. El Sayed, Abeer A. Sattar, Essam Abdel El Tanbouly, Nebal Sci Rep Article The objective of our study is to highlight the therapeutic effect and mechanism of action by which purified Flaxseed hydrolysate (PFH) which is a lignan rich fraction exerts its anticancer activity on a human breast cancer cell line (T47D) and in mice bearing tumor. HPLC analysis of PFH of six flaxseed cultivars had shown that PFH of the cultivar Giza 9 (PFH-G9) contains the highest concentration of SDG (81.64 mg/g). The in vitro cytotoxic potentiality of PFH’s of six flaxseed cultivars was screened against a panel of human cancer cell lines. PFH -G9 showed the most significant cytotoxic activity against ER-receptor positive breast cell lines MCF7 and T47D with IC(50) 13.8 and 15.8 µg/ml, respectively. Moreover, PFH-G9 reduced the expression of the metastasis marker, 1-α, metalloproteinases and vascular endothelial growth factor (VEGF), one of the most potent stimulators of angiogenesis, while it increased the caspase-3 dependent apoptosis. Our study also showed that dietary intake of 10% of Giza 9 Flaxseeds (FS), fixed oil (FSO) or Flax meal (FSM) twice daily for 3 weeks in mice-bearing solid Ehrlich ascites carcinoma (EAC) resulted in reducing the tumor volume, the expression of estrogen, insulin growth factor, progesterone, VEGF and MMP-2, but enhanced expression of caspase-3. Nature Publishing Group UK 2018-01-11 /pmc/articles/PMC5764973/ /pubmed/29323210 http://dx.doi.org/10.1038/s41598-017-18944-0 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ezzat, Shahira M.
Shouman, Samia A.
Elkhoely, Abeer
Attia, Yasmin M.
Elsesy, Mohamed S.
El Senousy, Amira S.
Choucry, Mouchira A.
El Gayed, Sabah H.
El Sayed, Abeer A.
Sattar, Essam Abdel
El Tanbouly, Nebal
Anticancer potentiality of lignan rich fraction of six Flaxseed cultivars
title Anticancer potentiality of lignan rich fraction of six Flaxseed cultivars
title_full Anticancer potentiality of lignan rich fraction of six Flaxseed cultivars
title_fullStr Anticancer potentiality of lignan rich fraction of six Flaxseed cultivars
title_full_unstemmed Anticancer potentiality of lignan rich fraction of six Flaxseed cultivars
title_short Anticancer potentiality of lignan rich fraction of six Flaxseed cultivars
title_sort anticancer potentiality of lignan rich fraction of six flaxseed cultivars
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764973/
https://www.ncbi.nlm.nih.gov/pubmed/29323210
http://dx.doi.org/10.1038/s41598-017-18944-0
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