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Ethyl Acetate Extracts of Semen Impatientis Inhibit Proliferation and Induce Apoptosis of Human Prostate Cancer Cell Lines through AKT/ERK Pathways

Objective. To investigate the inhibitory effect of ethyl acetate extracts of Impatiens balsamina L. on prostate cancer cells. Methods. Impatiens balsamina L. was extracted to get water, ethanol, oil ether, ethyl acetate, and butanol extracts. CCK-8 assay was used to detect the inhibitory effect. Apo...

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Autores principales: Wang, Tao, Cai, Yang, Song, Wen, Chen, Ruibao, Hu, Dunmei, Ye, Jianhan, Liu, Lu, Peng, Wei, Zhang, Junfeng, Wang, Shaogang, Yang, Weiming, Liu, Jihong, Ding, Yufeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5366801/
https://www.ncbi.nlm.nih.gov/pubmed/28386546
http://dx.doi.org/10.1155/2017/1243515
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author Wang, Tao
Cai, Yang
Song, Wen
Chen, Ruibao
Hu, Dunmei
Ye, Jianhan
Liu, Lu
Peng, Wei
Zhang, Junfeng
Wang, Shaogang
Yang, Weiming
Liu, Jihong
Ding, Yufeng
author_facet Wang, Tao
Cai, Yang
Song, Wen
Chen, Ruibao
Hu, Dunmei
Ye, Jianhan
Liu, Lu
Peng, Wei
Zhang, Junfeng
Wang, Shaogang
Yang, Weiming
Liu, Jihong
Ding, Yufeng
author_sort Wang, Tao
collection PubMed
description Objective. To investigate the inhibitory effect of ethyl acetate extracts of Impatiens balsamina L. on prostate cancer cells. Methods. Impatiens balsamina L. was extracted to get water, ethanol, oil ether, ethyl acetate, and butanol extracts. CCK-8 assay was used to detect the inhibitory effect. Apoptosis rates and cell cycle distribution were detected by flow cytometry. Transwell assay was performed to test the ability of migration. The expressions of Bcl-2, Bax, cleaved-caspase-3, p-ERK, ERK, p-AKT, AKT, cyclin D1, cyclin E, and MMP2 were detected by Western blot. Results. Ethyl acetate extracts had the strongest inhibitory effect. After being treated with different concentrations of ethyl acetate extracts, the percentage of G0/G1 phase increased significantly, cyclin D1 and cyclin E expression decreased, apoptosis rate was significantly higher, and the ability of migration of PC-3 and RV1 was inhibited significantly. Western blot showed that the expressions of Bcl-2, p-ERK, and p-AKT were significantly decreased, but the expressions of Bax and caspase-3 cleavage were increased. Conclusions. Impatiens balsamina L. inhibited the proliferation of human prostate cancer cells; ethyl acetate extracts have the strongest effect. It could inhibit cell proliferation and migration, cause G1 phase arrest, and induce apoptosis probably through inhibition of the AKT and ERK pathways.
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spelling pubmed-53668012017-04-06 Ethyl Acetate Extracts of Semen Impatientis Inhibit Proliferation and Induce Apoptosis of Human Prostate Cancer Cell Lines through AKT/ERK Pathways Wang, Tao Cai, Yang Song, Wen Chen, Ruibao Hu, Dunmei Ye, Jianhan Liu, Lu Peng, Wei Zhang, Junfeng Wang, Shaogang Yang, Weiming Liu, Jihong Ding, Yufeng Biomed Res Int Research Article Objective. To investigate the inhibitory effect of ethyl acetate extracts of Impatiens balsamina L. on prostate cancer cells. Methods. Impatiens balsamina L. was extracted to get water, ethanol, oil ether, ethyl acetate, and butanol extracts. CCK-8 assay was used to detect the inhibitory effect. Apoptosis rates and cell cycle distribution were detected by flow cytometry. Transwell assay was performed to test the ability of migration. The expressions of Bcl-2, Bax, cleaved-caspase-3, p-ERK, ERK, p-AKT, AKT, cyclin D1, cyclin E, and MMP2 were detected by Western blot. Results. Ethyl acetate extracts had the strongest inhibitory effect. After being treated with different concentrations of ethyl acetate extracts, the percentage of G0/G1 phase increased significantly, cyclin D1 and cyclin E expression decreased, apoptosis rate was significantly higher, and the ability of migration of PC-3 and RV1 was inhibited significantly. Western blot showed that the expressions of Bcl-2, p-ERK, and p-AKT were significantly decreased, but the expressions of Bax and caspase-3 cleavage were increased. Conclusions. Impatiens balsamina L. inhibited the proliferation of human prostate cancer cells; ethyl acetate extracts have the strongest effect. It could inhibit cell proliferation and migration, cause G1 phase arrest, and induce apoptosis probably through inhibition of the AKT and ERK pathways. Hindawi 2017 2017-03-13 /pmc/articles/PMC5366801/ /pubmed/28386546 http://dx.doi.org/10.1155/2017/1243515 Text en Copyright © 2017 Tao Wang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Tao
Cai, Yang
Song, Wen
Chen, Ruibao
Hu, Dunmei
Ye, Jianhan
Liu, Lu
Peng, Wei
Zhang, Junfeng
Wang, Shaogang
Yang, Weiming
Liu, Jihong
Ding, Yufeng
Ethyl Acetate Extracts of Semen Impatientis Inhibit Proliferation and Induce Apoptosis of Human Prostate Cancer Cell Lines through AKT/ERK Pathways
title Ethyl Acetate Extracts of Semen Impatientis Inhibit Proliferation and Induce Apoptosis of Human Prostate Cancer Cell Lines through AKT/ERK Pathways
title_full Ethyl Acetate Extracts of Semen Impatientis Inhibit Proliferation and Induce Apoptosis of Human Prostate Cancer Cell Lines through AKT/ERK Pathways
title_fullStr Ethyl Acetate Extracts of Semen Impatientis Inhibit Proliferation and Induce Apoptosis of Human Prostate Cancer Cell Lines through AKT/ERK Pathways
title_full_unstemmed Ethyl Acetate Extracts of Semen Impatientis Inhibit Proliferation and Induce Apoptosis of Human Prostate Cancer Cell Lines through AKT/ERK Pathways
title_short Ethyl Acetate Extracts of Semen Impatientis Inhibit Proliferation and Induce Apoptosis of Human Prostate Cancer Cell Lines through AKT/ERK Pathways
title_sort ethyl acetate extracts of semen impatientis inhibit proliferation and induce apoptosis of human prostate cancer cell lines through akt/erk pathways
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5366801/
https://www.ncbi.nlm.nih.gov/pubmed/28386546
http://dx.doi.org/10.1155/2017/1243515
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