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Antifungal and Cytotoxic Activity of Diterpenes and Bisnorsesquiterpenoides from the Latex of Euphorbia resinifera Berg.
Ourhzif, El-Mahdi; Ricelli, Alessandra; Stagni, Venturina; Cirigliano, Angela; Rinaldi, Teresa; Bouissane, Latifa; Saso, Luciano; Chalard, Pierre; Troin, Yves; Khouili, Mostafa; Akssira, Mohamed.
Afiliación
  • Ourhzif EM; Institut de Chimie de Clermont-Ferrand (ICCF), Dep. Chimie Organique et Medicinale, Université Clermont Auvergne CNRS SIGMA, F-63000 Clermont-Ferrand, France.
  • Ricelli A; Laboratoire de Chimie Physique et Biotechnologie des Biomolécules et des Matériaux, Faculté des Sciences et Techniques, Université Hassan II Casablanca, BP 146, Mohammedia 28800, Morocco.
  • Stagni V; Laboratoire de Chimie Moléculaire, Matériaux et Catalyse (LCMMC), Faculté des Sciences et Techniques, Université Sultan Moulay Slimane, BP 523, Beni-Mellal 23000, Morocco.
  • Cirigliano A; Institute of Molecular Biology and Pathology-CNR, P.le Aldo Moro, 5, 00185 Rome, Italy.
  • Rinaldi T; Institute of Molecular Biology and Pathology-CNR, P.le Aldo Moro, 5, 00185 Rome, Italy.
  • Bouissane L; Institute of Molecular Biology and Pathology-CNR, P.le Aldo Moro, 5, 00185 Rome, Italy.
  • Saso L; Department of Biology and Biotechnology, "Charles Darwin" Sapienza University, P.le Aldo Moro, 5, 00185 Rome, Italy.
  • Chalard P; Laboratoire de Chimie Moléculaire, Matériaux et Catalyse (LCMMC), Faculté des Sciences et Techniques, Université Sultan Moulay Slimane, BP 523, Beni-Mellal 23000, Morocco.
  • Troin Y; Department of Physiology and Pharmacology, "Vittorio Erspamer" Sapienza University, P.le Aldo Moro, 5, 00185 Rome, Italy.
  • Khouili M; Institut de Chimie de Clermont-Ferrand (ICCF), Dep. Chimie Organique et Medicinale, Université Clermont Auvergne CNRS SIGMA, F-63000 Clermont-Ferrand, France.
  • Akssira M; Institut de Chimie de Clermont-Ferrand (ICCF), Dep. Chimie Organique et Medicinale, Université Clermont Auvergne CNRS SIGMA, F-63000 Clermont-Ferrand, France.
Molecules ; 27(16)2022 Aug 16.
Article en En | MEDLINE | ID: mdl-36014466
ABSTRACT
Euphorbia resinifera latex has been extensively utilized in traditional medicine due to its range of bioactivities. Chromatographic separations on silica gel of ethanol extract of E. resinifera latex led to the development of a new procedure for isolating resiniferatoxin (4) via dried E. resinifera latex and the identification of nine compounds. Among these, catechol (7), protocatechuic acid (8) and 3,4-dihydroxyphenylacetic acid (9), known phenolic compounds, were identified for the first time in E. resinifera latex. Herein we investigated the effects of major compounds of the latex of E. resinifera on the yeast Saccharomyces cerevisiae, on the growth of Aspergillus carbonarius, a widespread fungal contaminant, and on the breast cancer cell line MCF7 as well as on MCF10A normal breast cells. 12-deoxyphorbol-13-isobutyrate-20-acetate (2) had an inhibiting effect on the growth of A. carbonarius, and 7-p-metoxyphenylacetate-3,8,12-triacetate ingol (3) showed a negative effect on yeast cell growth and also a cytotoxic effect on breast cancer cell line MCF7, but not on MCF10A cells. Deglucosyl euphorbioside A (5) and euphorbioside A (6) showed a discoloration effect that was possibly related to mitochondrial functionality in yeast, and also cytotoxicity only on the cancer cell line that was tested. Interestingly, treatment of MCF7 cells with 7-p-metoxyphenylacetate-3,8,12-triacetate ingol (3) and deglucosyl euphorbioside A (5) not only led to a specific cytotoxic effect but also to the increase in the level of intracellular ROS.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Euphorbia / Diterpenos / Antineoplásicos Límite: Female / Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Euphorbia / Diterpenos / Antineoplásicos Límite: Female / Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Francia
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