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Structure Identification and In Vitro Anticancer Activity of Lathyrol-3-phenylacetate-5,15-diacetate

Natural products from the genus Euphorbia show attention-attracting activities, such as anticancer activity. In this article, classical isolation and structure identification were used in a study on Caper Euphorbia Seed. Subsequently, MTT and wound healing assays, flow cytometry, western blotting, H...

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Autores principales: Zhang, Jian-ye, Huang, Wen-jing, Sun, Hong-mei, Liu, Yun, Zhao, Xiao-qin, Tang, Si-li, Sun, Ming-na, Wang, Sheng, Li, Jia-jun, Zhang, Ling-ling, Zhou, Jun-hua, Pan, Qian-rong, Chen, Hu-biao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151716/
https://www.ncbi.nlm.nih.gov/pubmed/28841191
http://dx.doi.org/10.3390/molecules22091412
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author Zhang, Jian-ye
Huang, Wen-jing
Sun, Hong-mei
Liu, Yun
Zhao, Xiao-qin
Tang, Si-li
Sun, Ming-na
Wang, Sheng
Li, Jia-jun
Zhang, Ling-ling
Zhou, Jun-hua
Pan, Qian-rong
Chen, Hu-biao
author_facet Zhang, Jian-ye
Huang, Wen-jing
Sun, Hong-mei
Liu, Yun
Zhao, Xiao-qin
Tang, Si-li
Sun, Ming-na
Wang, Sheng
Li, Jia-jun
Zhang, Ling-ling
Zhou, Jun-hua
Pan, Qian-rong
Chen, Hu-biao
author_sort Zhang, Jian-ye
collection PubMed
description Natural products from the genus Euphorbia show attention-attracting activities, such as anticancer activity. In this article, classical isolation and structure identification were used in a study on Caper Euphorbia Seed. Subsequently, MTT and wound healing assays, flow cytometry, western blotting, Hoechst 33258 staining and fluorescence microscopy examination were applied to investigate the anticancer activity of the obtained compounds. In a result, lathyrol-3-phenyl- acetate-5,15-diacetate (deoxy Euphorbia factor L1, DEFL1) was isolated from Caper Euphorbia Seed. Moreover, the NMR signals were totally assigned. DEFL1 showed potent inhibition against lung cancer A549 cells, with an IC(50) value of 17.51 ± 0.85 μM. Furthermore, DEFL1 suppressed wound healing of A549 cells in a concentration-dependent manner. Mechanically, DEFL1 induced apoptosis, with involvement of an increase of reactive oxygen species (ROS), decrease of mitochondrial membrane potential (ΔΨm), release of cytochrome c, activity raise of caspase-9 and 3. Characteristic features of apoptosis were observed by fluorescence microscopy. In summary, DEFL1 inhibited growth and induced apoptosis in lung cancer A549 cells via a mitochondrial pathway.
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spelling pubmed-61517162018-11-13 Structure Identification and In Vitro Anticancer Activity of Lathyrol-3-phenylacetate-5,15-diacetate Zhang, Jian-ye Huang, Wen-jing Sun, Hong-mei Liu, Yun Zhao, Xiao-qin Tang, Si-li Sun, Ming-na Wang, Sheng Li, Jia-jun Zhang, Ling-ling Zhou, Jun-hua Pan, Qian-rong Chen, Hu-biao Molecules Article Natural products from the genus Euphorbia show attention-attracting activities, such as anticancer activity. In this article, classical isolation and structure identification were used in a study on Caper Euphorbia Seed. Subsequently, MTT and wound healing assays, flow cytometry, western blotting, Hoechst 33258 staining and fluorescence microscopy examination were applied to investigate the anticancer activity of the obtained compounds. In a result, lathyrol-3-phenyl- acetate-5,15-diacetate (deoxy Euphorbia factor L1, DEFL1) was isolated from Caper Euphorbia Seed. Moreover, the NMR signals were totally assigned. DEFL1 showed potent inhibition against lung cancer A549 cells, with an IC(50) value of 17.51 ± 0.85 μM. Furthermore, DEFL1 suppressed wound healing of A549 cells in a concentration-dependent manner. Mechanically, DEFL1 induced apoptosis, with involvement of an increase of reactive oxygen species (ROS), decrease of mitochondrial membrane potential (ΔΨm), release of cytochrome c, activity raise of caspase-9 and 3. Characteristic features of apoptosis were observed by fluorescence microscopy. In summary, DEFL1 inhibited growth and induced apoptosis in lung cancer A549 cells via a mitochondrial pathway. MDPI 2017-08-25 /pmc/articles/PMC6151716/ /pubmed/28841191 http://dx.doi.org/10.3390/molecules22091412 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Jian-ye
Huang, Wen-jing
Sun, Hong-mei
Liu, Yun
Zhao, Xiao-qin
Tang, Si-li
Sun, Ming-na
Wang, Sheng
Li, Jia-jun
Zhang, Ling-ling
Zhou, Jun-hua
Pan, Qian-rong
Chen, Hu-biao
Structure Identification and In Vitro Anticancer Activity of Lathyrol-3-phenylacetate-5,15-diacetate
title Structure Identification and In Vitro Anticancer Activity of Lathyrol-3-phenylacetate-5,15-diacetate
title_full Structure Identification and In Vitro Anticancer Activity of Lathyrol-3-phenylacetate-5,15-diacetate
title_fullStr Structure Identification and In Vitro Anticancer Activity of Lathyrol-3-phenylacetate-5,15-diacetate
title_full_unstemmed Structure Identification and In Vitro Anticancer Activity of Lathyrol-3-phenylacetate-5,15-diacetate
title_short Structure Identification and In Vitro Anticancer Activity of Lathyrol-3-phenylacetate-5,15-diacetate
title_sort structure identification and in vitro anticancer activity of lathyrol-3-phenylacetate-5,15-diacetate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151716/
https://www.ncbi.nlm.nih.gov/pubmed/28841191
http://dx.doi.org/10.3390/molecules22091412
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