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Honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells
Honokiol (HNK) is a small organic molecule purified from magnolia species and has demonstrated anticancer activities in a variety of cancer cell lines; however, its effect on oral squamous cell carcinoma (OSCC) cells is unknown. We investigated the antitumor activities of HNK on OSCC cells in vitro...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469873/ https://www.ncbi.nlm.nih.gov/pubmed/21449214 http://dx.doi.org/10.4248/IJOS11014 |
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author | Chen, Xi-rui Lu, Rui Dan, Hong-xia Liao, Ga Zhou, Min Li, Xiao-yu Ji, Ning |
author_facet | Chen, Xi-rui Lu, Rui Dan, Hong-xia Liao, Ga Zhou, Min Li, Xiao-yu Ji, Ning |
author_sort | Chen, Xi-rui |
collection | PubMed |
description | Honokiol (HNK) is a small organic molecule purified from magnolia species and has demonstrated anticancer activities in a variety of cancer cell lines; however, its effect on oral squamous cell carcinoma (OSCC) cells is unknown. We investigated the antitumor activities of HNK on OSCC cells in vitro for the first time. The inhibitory effects of HNK on the growth and proliferation of OSCC cells were demonstrated via in vitro 3-(4,5-dimethyl thiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and propidium iodide (PI) assays, and the apoptotic cells were investigated by the observation of morphological changes and detection of DNA fragmentation via PI, TdT-mediated dUTP-biotin nick end labeling (TUNEL), and DNA ladder assays, as well as flow cytometry assay. The results showed that HNK inhibited the growth and proliferation of OSCC cells in vitro in a time and dose-dependent manner. The inhibitory effect was associated with the cell apoptosis induced by HNK, evidenced by the morphological features of apoptotic cells, TUNEL-positive cells and a degradation of chromosomal DNA into small internucleosomal fragments. The study also demonstrated here that the inhibition or apoptosis mediated by 15 μg·mL(−1) or 20 μg·mL(−1) of HNK were more stronger compared with those of 20 μg·mL(−1) 5-fluorouracil (5-Fu, the control) applied to OSCC cells, when the ratio of OSCC cell numbers were measured between the treatment of different concentrations of HNK to the 5-Fu treatment for 48 h. HNK is a promising compound that can be potentially used as a novel treatment agent for human OSCC. |
format | Online Article Text |
id | pubmed-3469873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34698732012-10-16 Honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells Chen, Xi-rui Lu, Rui Dan, Hong-xia Liao, Ga Zhou, Min Li, Xiao-yu Ji, Ning Int J Oral Sci Original Article Honokiol (HNK) is a small organic molecule purified from magnolia species and has demonstrated anticancer activities in a variety of cancer cell lines; however, its effect on oral squamous cell carcinoma (OSCC) cells is unknown. We investigated the antitumor activities of HNK on OSCC cells in vitro for the first time. The inhibitory effects of HNK on the growth and proliferation of OSCC cells were demonstrated via in vitro 3-(4,5-dimethyl thiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and propidium iodide (PI) assays, and the apoptotic cells were investigated by the observation of morphological changes and detection of DNA fragmentation via PI, TdT-mediated dUTP-biotin nick end labeling (TUNEL), and DNA ladder assays, as well as flow cytometry assay. The results showed that HNK inhibited the growth and proliferation of OSCC cells in vitro in a time and dose-dependent manner. The inhibitory effect was associated with the cell apoptosis induced by HNK, evidenced by the morphological features of apoptotic cells, TUNEL-positive cells and a degradation of chromosomal DNA into small internucleosomal fragments. The study also demonstrated here that the inhibition or apoptosis mediated by 15 μg·mL(−1) or 20 μg·mL(−1) of HNK were more stronger compared with those of 20 μg·mL(−1) 5-fluorouracil (5-Fu, the control) applied to OSCC cells, when the ratio of OSCC cell numbers were measured between the treatment of different concentrations of HNK to the 5-Fu treatment for 48 h. HNK is a promising compound that can be potentially used as a novel treatment agent for human OSCC. Nature Publishing Group 2011-01 /pmc/articles/PMC3469873/ /pubmed/21449214 http://dx.doi.org/10.4248/IJOS11014 Text en Copyright © 2011 West China School of Stomatology http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Chen, Xi-rui Lu, Rui Dan, Hong-xia Liao, Ga Zhou, Min Li, Xiao-yu Ji, Ning Honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells |
title | Honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells |
title_full | Honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells |
title_fullStr | Honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells |
title_full_unstemmed | Honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells |
title_short | Honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells |
title_sort | honokiol: a promising small molecular weight natural agent for the growth inhibition of oral squamous cell carcinoma cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469873/ https://www.ncbi.nlm.nih.gov/pubmed/21449214 http://dx.doi.org/10.4248/IJOS11014 |
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