Antiproliferation and Induction of Apoptosis in Ca9-22 Oral Cancer Cells by Ethanolic Extract of Gracilaria tenuistipitata
The water extract of Gracilaria tenuistipitata have been found to be protective against oxidative stress-induced cellular DNA damage, but the biological function of the ethanolic extracts of G. tenuistipitata (EEGT) is still unknown. In this study, the effect of EEGT on oral squamous cell cancer (OS...
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doaj-2696f53a41974f47bfa3dcd95fcc943b2020-11-24T22:30:32ZengMDPI AGMolecules1420-30492012-09-01179109161092710.3390/molecules170910916Antiproliferation and Induction of Apoptosis in Ca9-22 Oral Cancer Cells by Ethanolic Extract of Gracilaria tenuistipitataChi-Chen YehChao-Neng TsengJing-Iong YangHurng-Wern HuangYi FangJen-Yang TangFang-Rong ChangHsueh-Wei ChangThe water extract of Gracilaria tenuistipitata have been found to be protective against oxidative stress-induced cellular DNA damage, but the biological function of the ethanolic extracts of G. tenuistipitata (EEGT) is still unknown. In this study, the effect of EEGT on oral squamous cell cancer (OSCC) Ca9-22 cell line was examined in terms of the cell proliferation and oxidative stress responses. The cell viability of EEGT-treated OSCC cells was significantly reduced in a dose-response manner (p < 0.0001). The annexin V intensity and pan-caspase activity of EEGT-treated OSCC cells were significantly increased in a dose-response manner (p < 0.05 to 0.0001). EEGT significantly increased the reactive oxygen species (ROS) level (p < 0.0001) and decreased the glutathione (GSH) level (p < 0.01) in a dose-response manner. The mitochondrial membrane potential (MMP) of EEGT-treated OSCC cells was significantly decreased in a dose-response manner (p < 0.005). In conclusion, we have demonstrated that EEGT induced the growth inhibition and apoptosis of OSCC cells, which was accompanied by ROS increase, GSH depletion, caspase activation, and mitochondrial depolarization. Therefore, EEGT may have potent antitumor effect against oral cancer cells.http://www.mdpi.com/1420-3049/17/9/10916oral cancerapoptosisROSglutathionemitochondrial membrane potentialmarine natural product |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chi-Chen Yeh Chao-Neng Tseng Jing-Iong Yang Hurng-Wern Huang Yi Fang Jen-Yang Tang Fang-Rong Chang Hsueh-Wei Chang |
spellingShingle |
Chi-Chen Yeh Chao-Neng Tseng Jing-Iong Yang Hurng-Wern Huang Yi Fang Jen-Yang Tang Fang-Rong Chang Hsueh-Wei Chang Antiproliferation and Induction of Apoptosis in Ca9-22 Oral Cancer Cells by Ethanolic Extract of Gracilaria tenuistipitata Molecules oral cancer apoptosis ROS glutathione mitochondrial membrane potential marine natural product |
author_facet |
Chi-Chen Yeh Chao-Neng Tseng Jing-Iong Yang Hurng-Wern Huang Yi Fang Jen-Yang Tang Fang-Rong Chang Hsueh-Wei Chang |
author_sort |
Chi-Chen Yeh |
title |
Antiproliferation and Induction of Apoptosis in Ca9-22 Oral Cancer Cells by Ethanolic Extract of Gracilaria tenuistipitata |
title_short |
Antiproliferation and Induction of Apoptosis in Ca9-22 Oral Cancer Cells by Ethanolic Extract of Gracilaria tenuistipitata |
title_full |
Antiproliferation and Induction of Apoptosis in Ca9-22 Oral Cancer Cells by Ethanolic Extract of Gracilaria tenuistipitata |
title_fullStr |
Antiproliferation and Induction of Apoptosis in Ca9-22 Oral Cancer Cells by Ethanolic Extract of Gracilaria tenuistipitata |
title_full_unstemmed |
Antiproliferation and Induction of Apoptosis in Ca9-22 Oral Cancer Cells by Ethanolic Extract of Gracilaria tenuistipitata |
title_sort |
antiproliferation and induction of apoptosis in ca9-22 oral cancer cells by ethanolic extract of gracilaria tenuistipitata |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2012-09-01 |
description |
The water extract of Gracilaria tenuistipitata have been found to be protective against oxidative stress-induced cellular DNA damage, but the biological function of the ethanolic extracts of G. tenuistipitata (EEGT) is still unknown. In this study, the effect of EEGT on oral squamous cell cancer (OSCC) Ca9-22 cell line was examined in terms of the cell proliferation and oxidative stress responses. The cell viability of EEGT-treated OSCC cells was significantly reduced in a dose-response manner (p < 0.0001). The annexin V intensity and pan-caspase activity of EEGT-treated OSCC cells were significantly increased in a dose-response manner (p < 0.05 to 0.0001). EEGT significantly increased the reactive oxygen species (ROS) level (p < 0.0001) and decreased the glutathione (GSH) level (p < 0.01) in a dose-response manner. The mitochondrial membrane potential (MMP) of EEGT-treated OSCC cells was significantly decreased in a dose-response manner (p < 0.005). In conclusion, we have demonstrated that EEGT induced the growth inhibition and apoptosis of OSCC cells, which was accompanied by ROS increase, GSH depletion, caspase activation, and mitochondrial depolarization. Therefore, EEGT may have potent antitumor effect against oral cancer cells. |
topic |
oral cancer apoptosis ROS glutathione mitochondrial membrane potential marine natural product |
url |
http://www.mdpi.com/1420-3049/17/9/10916 |
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