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Sulforaphane Increases Cyclin-Dependent Kinase Inhibitor, p21 Protein in Human Oral Carcinoma Cells and Nude Mouse Animal Model to Induce G(2)/M Cell Cycle Arrest
Previously, our group reported that sulforaphane (SFN), a naturally occurring chemopreventive agent from cruciferous vegetables, effectively inhibits the proliferation of KB and YD-10B human oral squamous carcinoma cells by causing apoptosis. In this study, treatment of 20 and 40 µM of SFN for 12 h...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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the Society for Free Radical Research Japan
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2803134/ https://www.ncbi.nlm.nih.gov/pubmed/20104266 http://dx.doi.org/10.3164/jcbn.09-65 |
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author | Kim, Jun-Hee Han Kwon, Ki Jung, Ji-Youn Han, Hye-Suk Hyun Shim, Jung Oh, SeJun Choi, Kyeong-Hee Choi, Eun-Sun Shin, Ji-Ae Leem, Dae-Ho Soh, Yunjo Cho, Nam-Pyo Cho, Sung-Dae |
author_facet | Kim, Jun-Hee Han Kwon, Ki Jung, Ji-Youn Han, Hye-Suk Hyun Shim, Jung Oh, SeJun Choi, Kyeong-Hee Choi, Eun-Sun Shin, Ji-Ae Leem, Dae-Ho Soh, Yunjo Cho, Nam-Pyo Cho, Sung-Dae |
author_sort | Kim, Jun-Hee |
collection | PubMed |
description | Previously, our group reported that sulforaphane (SFN), a naturally occurring chemopreventive agent from cruciferous vegetables, effectively inhibits the proliferation of KB and YD-10B human oral squamous carcinoma cells by causing apoptosis. In this study, treatment of 20 and 40 µM of SFN for 12 h caused a cell cycle arrest in the G(2)/M phase. Cell cycle arrest induced by SFN was associated with a significant increase in the p21 protein level and a decrease in cyclin B expression, but there was no change in the cyclin A protein level. In addition, SFN increased the p21 promoter activity significantly. Furthermore, SFN induced p21 protein expression in a nude mouse xenograft model suggesting that SFN is a potent inducer of the p21 protein in human oral squamous carcinoma cells. These findings show that SFN is a promising candidate for molecular-targeting chemotherapy against human oral squamous cell carcinoma. |
format | Text |
id | pubmed-2803134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-28031342010-01-26 Sulforaphane Increases Cyclin-Dependent Kinase Inhibitor, p21 Protein in Human Oral Carcinoma Cells and Nude Mouse Animal Model to Induce G(2)/M Cell Cycle Arrest Kim, Jun-Hee Han Kwon, Ki Jung, Ji-Youn Han, Hye-Suk Hyun Shim, Jung Oh, SeJun Choi, Kyeong-Hee Choi, Eun-Sun Shin, Ji-Ae Leem, Dae-Ho Soh, Yunjo Cho, Nam-Pyo Cho, Sung-Dae J Clin Biochem Nutr Original Article Previously, our group reported that sulforaphane (SFN), a naturally occurring chemopreventive agent from cruciferous vegetables, effectively inhibits the proliferation of KB and YD-10B human oral squamous carcinoma cells by causing apoptosis. In this study, treatment of 20 and 40 µM of SFN for 12 h caused a cell cycle arrest in the G(2)/M phase. Cell cycle arrest induced by SFN was associated with a significant increase in the p21 protein level and a decrease in cyclin B expression, but there was no change in the cyclin A protein level. In addition, SFN increased the p21 promoter activity significantly. Furthermore, SFN induced p21 protein expression in a nude mouse xenograft model suggesting that SFN is a potent inducer of the p21 protein in human oral squamous carcinoma cells. These findings show that SFN is a promising candidate for molecular-targeting chemotherapy against human oral squamous cell carcinoma. the Society for Free Radical Research Japan 2010-01 2009-12-29 /pmc/articles/PMC2803134/ /pubmed/20104266 http://dx.doi.org/10.3164/jcbn.09-65 Text en Copyright © 2010 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Jun-Hee Han Kwon, Ki Jung, Ji-Youn Han, Hye-Suk Hyun Shim, Jung Oh, SeJun Choi, Kyeong-Hee Choi, Eun-Sun Shin, Ji-Ae Leem, Dae-Ho Soh, Yunjo Cho, Nam-Pyo Cho, Sung-Dae Sulforaphane Increases Cyclin-Dependent Kinase Inhibitor, p21 Protein in Human Oral Carcinoma Cells and Nude Mouse Animal Model to Induce G(2)/M Cell Cycle Arrest |
title | Sulforaphane Increases Cyclin-Dependent Kinase Inhibitor, p21 Protein in Human Oral Carcinoma Cells and Nude Mouse Animal Model to Induce G(2)/M Cell Cycle Arrest |
title_full | Sulforaphane Increases Cyclin-Dependent Kinase Inhibitor, p21 Protein in Human Oral Carcinoma Cells and Nude Mouse Animal Model to Induce G(2)/M Cell Cycle Arrest |
title_fullStr | Sulforaphane Increases Cyclin-Dependent Kinase Inhibitor, p21 Protein in Human Oral Carcinoma Cells and Nude Mouse Animal Model to Induce G(2)/M Cell Cycle Arrest |
title_full_unstemmed | Sulforaphane Increases Cyclin-Dependent Kinase Inhibitor, p21 Protein in Human Oral Carcinoma Cells and Nude Mouse Animal Model to Induce G(2)/M Cell Cycle Arrest |
title_short | Sulforaphane Increases Cyclin-Dependent Kinase Inhibitor, p21 Protein in Human Oral Carcinoma Cells and Nude Mouse Animal Model to Induce G(2)/M Cell Cycle Arrest |
title_sort | sulforaphane increases cyclin-dependent kinase inhibitor, p21 protein in human oral carcinoma cells and nude mouse animal model to induce g(2)/m cell cycle arrest |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2803134/ https://www.ncbi.nlm.nih.gov/pubmed/20104266 http://dx.doi.org/10.3164/jcbn.09-65 |
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