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Ingol and Ingenol-Type Diterpenes from Euphorbia trigona Miller with Keratinocyte Inhibitory Activity

Ingenol mebutate, isolated from Euphorbia peplus, is an ingenane-type diterpenoid, primarily used for the topical treatment of actinic keratosis, a premalignant skin condition. The aim of our work was to investigate other Euphorbia species to find structurally similar diterpenes that can be used as...

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Autores principales: Hammadi, Reham, Kúsz, Norbert, Dávid, Csilla Zsuzsanna, Behány, Zoltán, Papp, László, Kemény, Lajos, Hohmann, Judit, Lakatos, Lóránt, Vasas, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231945/
https://www.ncbi.nlm.nih.gov/pubmed/34198524
http://dx.doi.org/10.3390/plants10061206
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author Hammadi, Reham
Kúsz, Norbert
Dávid, Csilla Zsuzsanna
Behány, Zoltán
Papp, László
Kemény, Lajos
Hohmann, Judit
Lakatos, Lóránt
Vasas, Andrea
author_facet Hammadi, Reham
Kúsz, Norbert
Dávid, Csilla Zsuzsanna
Behány, Zoltán
Papp, László
Kemény, Lajos
Hohmann, Judit
Lakatos, Lóránt
Vasas, Andrea
author_sort Hammadi, Reham
collection PubMed
description Ingenol mebutate, isolated from Euphorbia peplus, is an ingenane-type diterpenoid, primarily used for the topical treatment of actinic keratosis, a premalignant skin condition. The aim of our work was to investigate other Euphorbia species to find structurally similar diterpenes that can be used as alternatives to ingenol mebutate. Pharmacological investigation of Euphorbia candelabrum, Euphorbia cotinifolia, Euphorbia ramipressa, and Euphorbia trigona revealed the potent keratinocyte (HPV-Ker cell line) inhibitory activity of these spurge species. From the methanolic extract of the aerial parts of Euphorbia trigona Miller, the most active species, five ingol (1–5) and four ingenane-type diterpenoids (6–9) were isolated by various chromatographic separation techniques, including open column chromatography, vacuum liquid chromatography, thin-layer chromatography, and high-performance liquid chromatography. The structures of the compounds were determined by NMR spectroscopic analysis and by comparison of the assignations with the literature data. The cytotoxic activity of the compounds against keratinocytes was tested in vitro by using ingenol mebutate as a positive control. Among the isolated compounds, two ingenane derivatives (6 and 7) exhibited remarkably stronger cytotoxic activity (IC(50) values 0.39 μM and 0.32 μM, respectively) on keratinocytes than ingenol mebutate (IC(50) value 0.84 μM). These compounds could serve as starting materials for further investigations to find alternatives to Picato(®) (with active substance ingenol mebutate), which was withdrawn from marketing authorization in the European Union.
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spelling pubmed-82319452021-06-26 Ingol and Ingenol-Type Diterpenes from Euphorbia trigona Miller with Keratinocyte Inhibitory Activity Hammadi, Reham Kúsz, Norbert Dávid, Csilla Zsuzsanna Behány, Zoltán Papp, László Kemény, Lajos Hohmann, Judit Lakatos, Lóránt Vasas, Andrea Plants (Basel) Article Ingenol mebutate, isolated from Euphorbia peplus, is an ingenane-type diterpenoid, primarily used for the topical treatment of actinic keratosis, a premalignant skin condition. The aim of our work was to investigate other Euphorbia species to find structurally similar diterpenes that can be used as alternatives to ingenol mebutate. Pharmacological investigation of Euphorbia candelabrum, Euphorbia cotinifolia, Euphorbia ramipressa, and Euphorbia trigona revealed the potent keratinocyte (HPV-Ker cell line) inhibitory activity of these spurge species. From the methanolic extract of the aerial parts of Euphorbia trigona Miller, the most active species, five ingol (1–5) and four ingenane-type diterpenoids (6–9) were isolated by various chromatographic separation techniques, including open column chromatography, vacuum liquid chromatography, thin-layer chromatography, and high-performance liquid chromatography. The structures of the compounds were determined by NMR spectroscopic analysis and by comparison of the assignations with the literature data. The cytotoxic activity of the compounds against keratinocytes was tested in vitro by using ingenol mebutate as a positive control. Among the isolated compounds, two ingenane derivatives (6 and 7) exhibited remarkably stronger cytotoxic activity (IC(50) values 0.39 μM and 0.32 μM, respectively) on keratinocytes than ingenol mebutate (IC(50) value 0.84 μM). These compounds could serve as starting materials for further investigations to find alternatives to Picato(®) (with active substance ingenol mebutate), which was withdrawn from marketing authorization in the European Union. MDPI 2021-06-14 /pmc/articles/PMC8231945/ /pubmed/34198524 http://dx.doi.org/10.3390/plants10061206 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hammadi, Reham
Kúsz, Norbert
Dávid, Csilla Zsuzsanna
Behány, Zoltán
Papp, László
Kemény, Lajos
Hohmann, Judit
Lakatos, Lóránt
Vasas, Andrea
Ingol and Ingenol-Type Diterpenes from Euphorbia trigona Miller with Keratinocyte Inhibitory Activity
title Ingol and Ingenol-Type Diterpenes from Euphorbia trigona Miller with Keratinocyte Inhibitory Activity
title_full Ingol and Ingenol-Type Diterpenes from Euphorbia trigona Miller with Keratinocyte Inhibitory Activity
title_fullStr Ingol and Ingenol-Type Diterpenes from Euphorbia trigona Miller with Keratinocyte Inhibitory Activity
title_full_unstemmed Ingol and Ingenol-Type Diterpenes from Euphorbia trigona Miller with Keratinocyte Inhibitory Activity
title_short Ingol and Ingenol-Type Diterpenes from Euphorbia trigona Miller with Keratinocyte Inhibitory Activity
title_sort ingol and ingenol-type diterpenes from euphorbia trigona miller with keratinocyte inhibitory activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231945/
https://www.ncbi.nlm.nih.gov/pubmed/34198524
http://dx.doi.org/10.3390/plants10061206
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