Cargando…

Anti-proliferative effect of isorhamnetin on HeLa cells through inducing G2/M cell cycle arrest

As a major cancer type in females, cervical cancer has been explored in depth by researchers. HeLa is a cervical cancer cell line. Isorhamnetin is an O-methylated flavonol that is primarily extracted from sea buckthorn. In the present study, the anti-proliferative effect of isorhamnetin on HeLa cell...

Descripción completa

Detalles Bibliográficos
Autores principales: Wei, Juan, Su, Hailan, Bi, Yang, Li, Jixin, Feng, Lidan, Sheng, Wenjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858116/
https://www.ncbi.nlm.nih.gov/pubmed/29563987
http://dx.doi.org/10.3892/etm.2018.5892
_version_ 1783307593600466944
author Wei, Juan
Su, Hailan
Bi, Yang
Li, Jixin
Feng, Lidan
Sheng, Wenjun
author_facet Wei, Juan
Su, Hailan
Bi, Yang
Li, Jixin
Feng, Lidan
Sheng, Wenjun
author_sort Wei, Juan
collection PubMed
description As a major cancer type in females, cervical cancer has been explored in depth by researchers. HeLa is a cervical cancer cell line. Isorhamnetin is an O-methylated flavonol that is primarily extracted from sea buckthorn. In the present study, the anti-proliferative effect of isorhamnetin on HeLa cells was evaluated using a Trypan blue dye exclusion assay. Isorhamnetin inhibited the cell proliferation in a time- and dose-dependent manner. Flow cytometric analysis of the cell cycle distribution revealed that isorhamnetin inhibited the cell cycle progression of HeLa by causing G2/M phase arrest and decreasing the proportion of cells in G1 phase. In addition, western blot analysis was performed to evaluate the presence of certain cell cycle-associated proteins. It was demonstrated that isorhamnetin inhibited the protein expression of cyclin B1, cell division cycle 25C (Cdc25C) and Cdc2, but enhanced checkpoint kinase 2 (Chk2), Cdc25C and Cdc2 phosphorylation. In addition, tubulin depolymerization participated in the isorhamnetin-induced cell cycle arrest in G2/M phase. In conclusion, the present results indicated that the anti-proliferative action of isorhamnetin is associated with arrest of the cell cycle in G2/M phase, which is a consequence of activation of the ataxia telangiectasia mutated Chk2 pathway and disruption of microtubule function.
format Online
Article
Text
id pubmed-5858116
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-58581162018-03-21 Anti-proliferative effect of isorhamnetin on HeLa cells through inducing G2/M cell cycle arrest Wei, Juan Su, Hailan Bi, Yang Li, Jixin Feng, Lidan Sheng, Wenjun Exp Ther Med Articles As a major cancer type in females, cervical cancer has been explored in depth by researchers. HeLa is a cervical cancer cell line. Isorhamnetin is an O-methylated flavonol that is primarily extracted from sea buckthorn. In the present study, the anti-proliferative effect of isorhamnetin on HeLa cells was evaluated using a Trypan blue dye exclusion assay. Isorhamnetin inhibited the cell proliferation in a time- and dose-dependent manner. Flow cytometric analysis of the cell cycle distribution revealed that isorhamnetin inhibited the cell cycle progression of HeLa by causing G2/M phase arrest and decreasing the proportion of cells in G1 phase. In addition, western blot analysis was performed to evaluate the presence of certain cell cycle-associated proteins. It was demonstrated that isorhamnetin inhibited the protein expression of cyclin B1, cell division cycle 25C (Cdc25C) and Cdc2, but enhanced checkpoint kinase 2 (Chk2), Cdc25C and Cdc2 phosphorylation. In addition, tubulin depolymerization participated in the isorhamnetin-induced cell cycle arrest in G2/M phase. In conclusion, the present results indicated that the anti-proliferative action of isorhamnetin is associated with arrest of the cell cycle in G2/M phase, which is a consequence of activation of the ataxia telangiectasia mutated Chk2 pathway and disruption of microtubule function. D.A. Spandidos 2018-04 2018-02-26 /pmc/articles/PMC5858116/ /pubmed/29563987 http://dx.doi.org/10.3892/etm.2018.5892 Text en Copyright: © Wei et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Wei, Juan
Su, Hailan
Bi, Yang
Li, Jixin
Feng, Lidan
Sheng, Wenjun
Anti-proliferative effect of isorhamnetin on HeLa cells through inducing G2/M cell cycle arrest
title Anti-proliferative effect of isorhamnetin on HeLa cells through inducing G2/M cell cycle arrest
title_full Anti-proliferative effect of isorhamnetin on HeLa cells through inducing G2/M cell cycle arrest
title_fullStr Anti-proliferative effect of isorhamnetin on HeLa cells through inducing G2/M cell cycle arrest
title_full_unstemmed Anti-proliferative effect of isorhamnetin on HeLa cells through inducing G2/M cell cycle arrest
title_short Anti-proliferative effect of isorhamnetin on HeLa cells through inducing G2/M cell cycle arrest
title_sort anti-proliferative effect of isorhamnetin on hela cells through inducing g2/m cell cycle arrest
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858116/
https://www.ncbi.nlm.nih.gov/pubmed/29563987
http://dx.doi.org/10.3892/etm.2018.5892
work_keys_str_mv AT weijuan antiproliferativeeffectofisorhamnetinonhelacellsthroughinducingg2mcellcyclearrest
AT suhailan antiproliferativeeffectofisorhamnetinonhelacellsthroughinducingg2mcellcyclearrest
AT biyang antiproliferativeeffectofisorhamnetinonhelacellsthroughinducingg2mcellcyclearrest
AT lijixin antiproliferativeeffectofisorhamnetinonhelacellsthroughinducingg2mcellcyclearrest
AT fenglidan antiproliferativeeffectofisorhamnetinonhelacellsthroughinducingg2mcellcyclearrest
AT shengwenjun antiproliferativeeffectofisorhamnetinonhelacellsthroughinducingg2mcellcyclearrest