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Anticancer effect of Saussurea lappa extract via dual control of apoptosis and autophagy in prostate cancer cells
To demonstrate the mechanisms of the curative effect of Saussurea lappa ethanol extract (SLE) against prostate cancer, we evaluated the effect of SLE on the induction of apoptosis and autophagy and investigated whether SLE-induced autophagy exerts a pro-survival or pro-apoptotic effect in lymph node...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627836/ https://www.ncbi.nlm.nih.gov/pubmed/28746210 http://dx.doi.org/10.1097/MD.0000000000007606 |
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author | Tian, Xue Song, Hae Seong Cho, Young Mi Park, Bongkyun Song, Yoon-Jae Jang, Sunphil Kang, Se Chan |
author_facet | Tian, Xue Song, Hae Seong Cho, Young Mi Park, Bongkyun Song, Yoon-Jae Jang, Sunphil Kang, Se Chan |
author_sort | Tian, Xue |
collection | PubMed |
description | To demonstrate the mechanisms of the curative effect of Saussurea lappa ethanol extract (SLE) against prostate cancer, we evaluated the effect of SLE on the induction of apoptosis and autophagy and investigated whether SLE-induced autophagy exerts a pro-survival or pro-apoptotic effect in lymph node carcinoma of the prostate (LNCaP) prostate cancer cells. SLE was prepared using 100% ethanol and added to LNCaP cells for 24 hours. Cell viability was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, and cell apoptosis was evaluated by Tali assay. The expression of apoptosis-related mRNA and proteins was analyzed by quantitative real-time RT-PCR and western blotting. SLE treatment decreased the viability of LNCaP cells and increased Bax expression while suppressing the expression of pro-caspases-8/9/3, PARP, Bid, and Bcl-2, thereby inducing apoptosis in LNCaP cells. Cell proliferation related proteins, including p-Akt, androgen receptor, and prostate-specific antigen, were suppressed by SLE treatment. SLE also induced autophagy in LNCaP cells, and inhibition of autophagy enhanced the apoptosis induced by SLE treatment. These results suggest that SLE exerts anticancer effects through the induction of both cellular apoptosis and autophagy, and apoptotic cell death can be facilitated by blocking autophagy in SLE-treated LNCaP cells. Therefore, SLE might be a potential anticancer agent for the treatment of prostate cancer. |
format | Online Article Text |
id | pubmed-5627836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-56278362017-10-12 Anticancer effect of Saussurea lappa extract via dual control of apoptosis and autophagy in prostate cancer cells Tian, Xue Song, Hae Seong Cho, Young Mi Park, Bongkyun Song, Yoon-Jae Jang, Sunphil Kang, Se Chan Medicine (Baltimore) 5700 To demonstrate the mechanisms of the curative effect of Saussurea lappa ethanol extract (SLE) against prostate cancer, we evaluated the effect of SLE on the induction of apoptosis and autophagy and investigated whether SLE-induced autophagy exerts a pro-survival or pro-apoptotic effect in lymph node carcinoma of the prostate (LNCaP) prostate cancer cells. SLE was prepared using 100% ethanol and added to LNCaP cells for 24 hours. Cell viability was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, and cell apoptosis was evaluated by Tali assay. The expression of apoptosis-related mRNA and proteins was analyzed by quantitative real-time RT-PCR and western blotting. SLE treatment decreased the viability of LNCaP cells and increased Bax expression while suppressing the expression of pro-caspases-8/9/3, PARP, Bid, and Bcl-2, thereby inducing apoptosis in LNCaP cells. Cell proliferation related proteins, including p-Akt, androgen receptor, and prostate-specific antigen, were suppressed by SLE treatment. SLE also induced autophagy in LNCaP cells, and inhibition of autophagy enhanced the apoptosis induced by SLE treatment. These results suggest that SLE exerts anticancer effects through the induction of both cellular apoptosis and autophagy, and apoptotic cell death can be facilitated by blocking autophagy in SLE-treated LNCaP cells. Therefore, SLE might be a potential anticancer agent for the treatment of prostate cancer. Wolters Kluwer Health 2017-07-28 /pmc/articles/PMC5627836/ /pubmed/28746210 http://dx.doi.org/10.1097/MD.0000000000007606 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0 |
spellingShingle | 5700 Tian, Xue Song, Hae Seong Cho, Young Mi Park, Bongkyun Song, Yoon-Jae Jang, Sunphil Kang, Se Chan Anticancer effect of Saussurea lappa extract via dual control of apoptosis and autophagy in prostate cancer cells |
title | Anticancer effect of Saussurea lappa extract via dual control of apoptosis and autophagy in prostate cancer cells |
title_full | Anticancer effect of Saussurea lappa extract via dual control of apoptosis and autophagy in prostate cancer cells |
title_fullStr | Anticancer effect of Saussurea lappa extract via dual control of apoptosis and autophagy in prostate cancer cells |
title_full_unstemmed | Anticancer effect of Saussurea lappa extract via dual control of apoptosis and autophagy in prostate cancer cells |
title_short | Anticancer effect of Saussurea lappa extract via dual control of apoptosis and autophagy in prostate cancer cells |
title_sort | anticancer effect of saussurea lappa extract via dual control of apoptosis and autophagy in prostate cancer cells |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627836/ https://www.ncbi.nlm.nih.gov/pubmed/28746210 http://dx.doi.org/10.1097/MD.0000000000007606 |
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