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Inhibitory effects of garcinone E on fatty acid synthase

Fatty acid synthase (FAS) is highly expressed in human adipocytes and cancer cells and is considered as a dual therapeutic target for obesity and cancer treatment. Garcinone E is a natural xanthone and exists in the pericarp of Garcinia mangostana. In previous studies, xanthones were reported to be...

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Detalles Bibliográficos
Autores principales: Liang, Yan, Luo, Di, Gao, Xuan, Wu, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078525/
https://www.ncbi.nlm.nih.gov/pubmed/35542030
http://dx.doi.org/10.1039/c7ra13246h
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author Liang, Yan
Luo, Di
Gao, Xuan
Wu, Hao
author_facet Liang, Yan
Luo, Di
Gao, Xuan
Wu, Hao
author_sort Liang, Yan
collection PubMed
description Fatty acid synthase (FAS) is highly expressed in human adipocytes and cancer cells and is considered as a dual therapeutic target for obesity and cancer treatment. Garcinone E is a natural xanthone and exists in the pericarp of Garcinia mangostana. In previous studies, xanthones were reported to be highly active inhibitors of FAS. In the present study, the detailed inhibitory mechanism of garcinone E on FAS was investigated. We found that garcinone E inhibited the activity of FAS in a concentration-dependent manner with a half-inhibitory concentration value of 3.3 μM. The inhibition kinetic results showed that the inhibition of FAS by garcinone E was competitive with respect to acetyl-CoA, mixed competitive and noncompetitive with respect to malonyl-CoA, and noncompetitive to NADPH. In addition, garcinone E showed irreversible inhibition on FAS, which was different from all other xanthones. Since FAS is believed to be a therapeutic target for obesity and cancer treatment, these findings suggest the clinical potential of garcinone E in the prevention and treatment of both obesity and cancer.
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spelling pubmed-90785252022-05-09 Inhibitory effects of garcinone E on fatty acid synthase Liang, Yan Luo, Di Gao, Xuan Wu, Hao RSC Adv Chemistry Fatty acid synthase (FAS) is highly expressed in human adipocytes and cancer cells and is considered as a dual therapeutic target for obesity and cancer treatment. Garcinone E is a natural xanthone and exists in the pericarp of Garcinia mangostana. In previous studies, xanthones were reported to be highly active inhibitors of FAS. In the present study, the detailed inhibitory mechanism of garcinone E on FAS was investigated. We found that garcinone E inhibited the activity of FAS in a concentration-dependent manner with a half-inhibitory concentration value of 3.3 μM. The inhibition kinetic results showed that the inhibition of FAS by garcinone E was competitive with respect to acetyl-CoA, mixed competitive and noncompetitive with respect to malonyl-CoA, and noncompetitive to NADPH. In addition, garcinone E showed irreversible inhibition on FAS, which was different from all other xanthones. Since FAS is believed to be a therapeutic target for obesity and cancer treatment, these findings suggest the clinical potential of garcinone E in the prevention and treatment of both obesity and cancer. The Royal Society of Chemistry 2018-02-20 /pmc/articles/PMC9078525/ /pubmed/35542030 http://dx.doi.org/10.1039/c7ra13246h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Liang, Yan
Luo, Di
Gao, Xuan
Wu, Hao
Inhibitory effects of garcinone E on fatty acid synthase
title Inhibitory effects of garcinone E on fatty acid synthase
title_full Inhibitory effects of garcinone E on fatty acid synthase
title_fullStr Inhibitory effects of garcinone E on fatty acid synthase
title_full_unstemmed Inhibitory effects of garcinone E on fatty acid synthase
title_short Inhibitory effects of garcinone E on fatty acid synthase
title_sort inhibitory effects of garcinone e on fatty acid synthase
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078525/
https://www.ncbi.nlm.nih.gov/pubmed/35542030
http://dx.doi.org/10.1039/c7ra13246h
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