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The antiangiogenic activities of ethanolic crude extracts of four Salvia species

BACKGROUND: Angiogenesis is one of cancer hallmarks that are required for both cancer progression and metastasis. In this study we examined the antiangiogenic properties of the ethanolic crude extracts of four Salvia species grown in Jordan. METHODS: The direct antiangiogenic activity was evaluated...

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Autores principales: Zihlif, Malek, Afifi, Fatma, Abu-Dahab, Rana, Abdul Majid, Amin Malik Shah, Somrain, Hamza, Saleh, Mohanad M, Nassar, Zeyad D, Naffa, Randa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878736/
https://www.ncbi.nlm.nih.gov/pubmed/24330494
http://dx.doi.org/10.1186/1472-6882-13-358
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author Zihlif, Malek
Afifi, Fatma
Abu-Dahab, Rana
Abdul Majid, Amin Malik Shah
Somrain, Hamza
Saleh, Mohanad M
Nassar, Zeyad D
Naffa, Randa
author_facet Zihlif, Malek
Afifi, Fatma
Abu-Dahab, Rana
Abdul Majid, Amin Malik Shah
Somrain, Hamza
Saleh, Mohanad M
Nassar, Zeyad D
Naffa, Randa
author_sort Zihlif, Malek
collection PubMed
description BACKGROUND: Angiogenesis is one of cancer hallmarks that are required for both cancer progression and metastasis. In this study we examined the antiangiogenic properties of the ethanolic crude extracts of four Salvia species grown in Jordan. METHODS: The direct antiangiogenic activity was evaluated using various models: ex vivo rat aortic ring assay, in vitro assessment of HUVEC proliferation and migration, and in vivo CAM assay, while we used the changes in the expression of HIF-1α and VEGF in breast cancer cells (MCF 7) as an indicative for the indirect antiangiogenic activity. RESULTS: All four crude extracts showed a potential antiangiogenic activity in the rat aortic assay, however two species were found to be cytotoxic against Fibroblast cell line (PLF); the finding that caused the exclusion of these two extracts from further studies. Of the two remaining extracts, S. triloba showed very promising direct and indirect antiangiogenic activities. S. triloba inhibited the HUVEC proliferation with an IC(50) of 90 μg/mL and HUVEC migration by 82% at 150 μg/mL. Furthermore, the in vivo CAM assay also illustrated the high impact of S. triloba against the newly formed vessel in the chicken embryonic membrane. Interestingly, the S. triloba inhibited the expression of VEGF at the mRNA and protein and the HIF-1α mRNA in the MCF 7 breast cancer cells under both normoxic and hypoxic conditions. CONCLUSIONS: Taken together, all these findings of the direct and indirect angiogenic investigations nominated S. triloba as a highly potent antiangiogenic plant that may have chemotherapeutic and/or chemoprevention potentials.
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spelling pubmed-38787362014-01-03 The antiangiogenic activities of ethanolic crude extracts of four Salvia species Zihlif, Malek Afifi, Fatma Abu-Dahab, Rana Abdul Majid, Amin Malik Shah Somrain, Hamza Saleh, Mohanad M Nassar, Zeyad D Naffa, Randa BMC Complement Altern Med Research Article BACKGROUND: Angiogenesis is one of cancer hallmarks that are required for both cancer progression and metastasis. In this study we examined the antiangiogenic properties of the ethanolic crude extracts of four Salvia species grown in Jordan. METHODS: The direct antiangiogenic activity was evaluated using various models: ex vivo rat aortic ring assay, in vitro assessment of HUVEC proliferation and migration, and in vivo CAM assay, while we used the changes in the expression of HIF-1α and VEGF in breast cancer cells (MCF 7) as an indicative for the indirect antiangiogenic activity. RESULTS: All four crude extracts showed a potential antiangiogenic activity in the rat aortic assay, however two species were found to be cytotoxic against Fibroblast cell line (PLF); the finding that caused the exclusion of these two extracts from further studies. Of the two remaining extracts, S. triloba showed very promising direct and indirect antiangiogenic activities. S. triloba inhibited the HUVEC proliferation with an IC(50) of 90 μg/mL and HUVEC migration by 82% at 150 μg/mL. Furthermore, the in vivo CAM assay also illustrated the high impact of S. triloba against the newly formed vessel in the chicken embryonic membrane. Interestingly, the S. triloba inhibited the expression of VEGF at the mRNA and protein and the HIF-1α mRNA in the MCF 7 breast cancer cells under both normoxic and hypoxic conditions. CONCLUSIONS: Taken together, all these findings of the direct and indirect angiogenic investigations nominated S. triloba as a highly potent antiangiogenic plant that may have chemotherapeutic and/or chemoprevention potentials. BioMed Central 2013-12-13 /pmc/articles/PMC3878736/ /pubmed/24330494 http://dx.doi.org/10.1186/1472-6882-13-358 Text en Copyright © 2013 Zihlif et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zihlif, Malek
Afifi, Fatma
Abu-Dahab, Rana
Abdul Majid, Amin Malik Shah
Somrain, Hamza
Saleh, Mohanad M
Nassar, Zeyad D
Naffa, Randa
The antiangiogenic activities of ethanolic crude extracts of four Salvia species
title The antiangiogenic activities of ethanolic crude extracts of four Salvia species
title_full The antiangiogenic activities of ethanolic crude extracts of four Salvia species
title_fullStr The antiangiogenic activities of ethanolic crude extracts of four Salvia species
title_full_unstemmed The antiangiogenic activities of ethanolic crude extracts of four Salvia species
title_short The antiangiogenic activities of ethanolic crude extracts of four Salvia species
title_sort antiangiogenic activities of ethanolic crude extracts of four salvia species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878736/
https://www.ncbi.nlm.nih.gov/pubmed/24330494
http://dx.doi.org/10.1186/1472-6882-13-358
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