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Antiproliferative activity of spinasterol isolated of Stegnosperma halimifolium (Benth, 1844)

Cancer is the major cause of death in the world, representing a significant public health problem. Plants have been shown as a great source of secondary metabolites with anticancer activity. The aim of this work was evaluated the antiproliferative activity of the methanolic extracts, chemical fracti...

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Autores principales: Meneses-Sagrero, Salvador Enrique, Navarro-Navarro, Moisés, Ruiz-Bustos, Eduardo, Del-Toro-Sánchez, Carmen Lizette, Jiménez-Estrada, Manuel, Robles-Zepeda, Ramón Enrique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6111116/
https://www.ncbi.nlm.nih.gov/pubmed/30166901
http://dx.doi.org/10.1016/j.jsps.2017.07.001
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author Meneses-Sagrero, Salvador Enrique
Navarro-Navarro, Moisés
Ruiz-Bustos, Eduardo
Del-Toro-Sánchez, Carmen Lizette
Jiménez-Estrada, Manuel
Robles-Zepeda, Ramón Enrique
author_facet Meneses-Sagrero, Salvador Enrique
Navarro-Navarro, Moisés
Ruiz-Bustos, Eduardo
Del-Toro-Sánchez, Carmen Lizette
Jiménez-Estrada, Manuel
Robles-Zepeda, Ramón Enrique
author_sort Meneses-Sagrero, Salvador Enrique
collection PubMed
description Cancer is the major cause of death in the world, representing a significant public health problem. Plants have been shown as a great source of secondary metabolites with anticancer activity. The aim of this work was evaluated the antiproliferative activity of the methanolic extracts, chemical fractions and the compound spinasterol isolated of medicinal plant Stegnosperma halimifolium. The methanolic extracts of stem, leaf and stem/leaf was obtained by maceration. The methanolic extract of stem was purified by successive extractions with solvents as n-hexane, ethyl acetate and ethanol. The n-hexane fraction was separated by column chromatographic and monitored by thin layer chromatographic. The compound spinasterol was characterized by (1)H NMR, (13)C NMR and Mass Spectrometry. Methanolic extracts, chemical, chromatographic fractions and spinasterol was evaluated against RAW 264.7, M12.C3.F6, PC-3, LS-180, A549 and HeLa cancer cell lines by the standardized method MTT for determinate the antiproliferative activity. Methanolic extract of stem shown the better antiproliferative activity against the murine macrophage cancer cell line RAW 264.7. n-Hexane chemical fraction shown antiproliferative activity against human alveolar cancer cell line A549 and RAW 264.7. Was isolated and characterized a compound by NMR (1)H and (13)C, revealing the presence of sterol spinasterol. Spinasterol shown to have antiproliferative activity against cervical cancer cell line HeLa and RAW 264.7, indicating that spinasterol can be a responsible compound of antiproliferative activity found in the methanolic extract of Stegnosperma halimifolium.
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spelling pubmed-61111162018-08-30 Antiproliferative activity of spinasterol isolated of Stegnosperma halimifolium (Benth, 1844) Meneses-Sagrero, Salvador Enrique Navarro-Navarro, Moisés Ruiz-Bustos, Eduardo Del-Toro-Sánchez, Carmen Lizette Jiménez-Estrada, Manuel Robles-Zepeda, Ramón Enrique Saudi Pharm J Article Cancer is the major cause of death in the world, representing a significant public health problem. Plants have been shown as a great source of secondary metabolites with anticancer activity. The aim of this work was evaluated the antiproliferative activity of the methanolic extracts, chemical fractions and the compound spinasterol isolated of medicinal plant Stegnosperma halimifolium. The methanolic extracts of stem, leaf and stem/leaf was obtained by maceration. The methanolic extract of stem was purified by successive extractions with solvents as n-hexane, ethyl acetate and ethanol. The n-hexane fraction was separated by column chromatographic and monitored by thin layer chromatographic. The compound spinasterol was characterized by (1)H NMR, (13)C NMR and Mass Spectrometry. Methanolic extracts, chemical, chromatographic fractions and spinasterol was evaluated against RAW 264.7, M12.C3.F6, PC-3, LS-180, A549 and HeLa cancer cell lines by the standardized method MTT for determinate the antiproliferative activity. Methanolic extract of stem shown the better antiproliferative activity against the murine macrophage cancer cell line RAW 264.7. n-Hexane chemical fraction shown antiproliferative activity against human alveolar cancer cell line A549 and RAW 264.7. Was isolated and characterized a compound by NMR (1)H and (13)C, revealing the presence of sterol spinasterol. Spinasterol shown to have antiproliferative activity against cervical cancer cell line HeLa and RAW 264.7, indicating that spinasterol can be a responsible compound of antiproliferative activity found in the methanolic extract of Stegnosperma halimifolium. Elsevier 2017-12 2017-07-11 /pmc/articles/PMC6111116/ /pubmed/30166901 http://dx.doi.org/10.1016/j.jsps.2017.07.001 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Meneses-Sagrero, Salvador Enrique
Navarro-Navarro, Moisés
Ruiz-Bustos, Eduardo
Del-Toro-Sánchez, Carmen Lizette
Jiménez-Estrada, Manuel
Robles-Zepeda, Ramón Enrique
Antiproliferative activity of spinasterol isolated of Stegnosperma halimifolium (Benth, 1844)
title Antiproliferative activity of spinasterol isolated of Stegnosperma halimifolium (Benth, 1844)
title_full Antiproliferative activity of spinasterol isolated of Stegnosperma halimifolium (Benth, 1844)
title_fullStr Antiproliferative activity of spinasterol isolated of Stegnosperma halimifolium (Benth, 1844)
title_full_unstemmed Antiproliferative activity of spinasterol isolated of Stegnosperma halimifolium (Benth, 1844)
title_short Antiproliferative activity of spinasterol isolated of Stegnosperma halimifolium (Benth, 1844)
title_sort antiproliferative activity of spinasterol isolated of stegnosperma halimifolium (benth, 1844)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6111116/
https://www.ncbi.nlm.nih.gov/pubmed/30166901
http://dx.doi.org/10.1016/j.jsps.2017.07.001
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