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Limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16(INK4A) re-expression related to UHRF1 and DNMT1 down-regulation

Several reports have described the potential effects of natural compounds as anti-cancer agents in vitro as well as in vivo. The aim of this study was to evaluate the anti-cancer effect of Limoniastrum guyonianum aqueous gall extract (G extract) and luteolin in the human cervical cancer HeLa cell li...

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Autores principales: Krifa, Mounira, Alhosin, Mahmoud, Muller, Christian D, Gies, Jean-Pierre, Chekir-Ghedira, Leila, Ghedira, Kamel, Mély, Yves, Bronner, Christian, Mousli, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695779/
https://www.ncbi.nlm.nih.gov/pubmed/23688286
http://dx.doi.org/10.1186/1756-9966-32-30
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author Krifa, Mounira
Alhosin, Mahmoud
Muller, Christian D
Gies, Jean-Pierre
Chekir-Ghedira, Leila
Ghedira, Kamel
Mély, Yves
Bronner, Christian
Mousli, Marc
author_facet Krifa, Mounira
Alhosin, Mahmoud
Muller, Christian D
Gies, Jean-Pierre
Chekir-Ghedira, Leila
Ghedira, Kamel
Mély, Yves
Bronner, Christian
Mousli, Marc
author_sort Krifa, Mounira
collection PubMed
description Several reports have described the potential effects of natural compounds as anti-cancer agents in vitro as well as in vivo. The aim of this study was to evaluate the anti-cancer effect of Limoniastrum guyonianum aqueous gall extract (G extract) and luteolin in the human cervical cancer HeLa cell line, and, if so, to clarify the underlying mechanism. Our results show that G extract and luteolin inhibited cell proliferation and induced G2/M cell cycle arrest in a concentration and time-dependent manner. Both natural products induced programmed cell death as confirmed by the presence of hypodiploid G0/G1 cells. These effects are associated with an up-regulation of the expression of the tumor suppressor gene p16(INK4A) and a down-regulation of the expression of the anti-apoptotic actor UHRF1 and its main partner DNMT1. Moreover, G extract- and luteolin-induced UHRF1 and DNMT1 down-regulation is accompanied with a global DNA hypomethylation in HeLa cell line. Altogether our results show that G extract mediates its growth inhibitory effects on human cervical cancer HeLa cell line likely via the activation of a p16(INK4A) -dependent cell cycle checkpoint signalling pathway orchestrated by UHRF1 and DNMT1 down-regulation.
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spelling pubmed-36957792013-06-29 Limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16(INK4A) re-expression related to UHRF1 and DNMT1 down-regulation Krifa, Mounira Alhosin, Mahmoud Muller, Christian D Gies, Jean-Pierre Chekir-Ghedira, Leila Ghedira, Kamel Mély, Yves Bronner, Christian Mousli, Marc J Exp Clin Cancer Res Research Several reports have described the potential effects of natural compounds as anti-cancer agents in vitro as well as in vivo. The aim of this study was to evaluate the anti-cancer effect of Limoniastrum guyonianum aqueous gall extract (G extract) and luteolin in the human cervical cancer HeLa cell line, and, if so, to clarify the underlying mechanism. Our results show that G extract and luteolin inhibited cell proliferation and induced G2/M cell cycle arrest in a concentration and time-dependent manner. Both natural products induced programmed cell death as confirmed by the presence of hypodiploid G0/G1 cells. These effects are associated with an up-regulation of the expression of the tumor suppressor gene p16(INK4A) and a down-regulation of the expression of the anti-apoptotic actor UHRF1 and its main partner DNMT1. Moreover, G extract- and luteolin-induced UHRF1 and DNMT1 down-regulation is accompanied with a global DNA hypomethylation in HeLa cell line. Altogether our results show that G extract mediates its growth inhibitory effects on human cervical cancer HeLa cell line likely via the activation of a p16(INK4A) -dependent cell cycle checkpoint signalling pathway orchestrated by UHRF1 and DNMT1 down-regulation. BioMed Central 2013-05-20 /pmc/articles/PMC3695779/ /pubmed/23688286 http://dx.doi.org/10.1186/1756-9966-32-30 Text en Copyright © 2013 Krifa et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Krifa, Mounira
Alhosin, Mahmoud
Muller, Christian D
Gies, Jean-Pierre
Chekir-Ghedira, Leila
Ghedira, Kamel
Mély, Yves
Bronner, Christian
Mousli, Marc
Limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16(INK4A) re-expression related to UHRF1 and DNMT1 down-regulation
title Limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16(INK4A) re-expression related to UHRF1 and DNMT1 down-regulation
title_full Limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16(INK4A) re-expression related to UHRF1 and DNMT1 down-regulation
title_fullStr Limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16(INK4A) re-expression related to UHRF1 and DNMT1 down-regulation
title_full_unstemmed Limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16(INK4A) re-expression related to UHRF1 and DNMT1 down-regulation
title_short Limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16(INK4A) re-expression related to UHRF1 and DNMT1 down-regulation
title_sort limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16(ink4a) re-expression related to uhrf1 and dnmt1 down-regulation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695779/
https://www.ncbi.nlm.nih.gov/pubmed/23688286
http://dx.doi.org/10.1186/1756-9966-32-30
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