Cargando…
Oridonin induces apoptosis and cell cycle arrest of gallbladder cancer cells via the mitochondrial pathway
BACKGROUND: Gallbladder cancer is the most frequent malignancy of the bile duct with high aggressive and extremely poor prognosis. The main objective of the paper was to investigate the inhibitory effects of oridonin, a diterpenoid isolated from Rabdosia rubescens, on gallbladder cancer both in vitr...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994450/ https://www.ncbi.nlm.nih.gov/pubmed/24655726 http://dx.doi.org/10.1186/1471-2407-14-217 |
_version_ | 1782312729686573056 |
---|---|
author | Bao, Runfa Shu, Yijun Wu, Xiangsong Weng, Hao Ding, Qian Cao, Yang Li, Maolan Mu, Jiasheng Wu, Wenguang Ding, Qichen Tan, Zhujun Liu, Tianyu Jiang, Lin Hu, Yunping Gu, Jianfeng Liu, Yingbin |
author_facet | Bao, Runfa Shu, Yijun Wu, Xiangsong Weng, Hao Ding, Qian Cao, Yang Li, Maolan Mu, Jiasheng Wu, Wenguang Ding, Qichen Tan, Zhujun Liu, Tianyu Jiang, Lin Hu, Yunping Gu, Jianfeng Liu, Yingbin |
author_sort | Bao, Runfa |
collection | PubMed |
description | BACKGROUND: Gallbladder cancer is the most frequent malignancy of the bile duct with high aggressive and extremely poor prognosis. The main objective of the paper was to investigate the inhibitory effects of oridonin, a diterpenoid isolated from Rabdosia rubescens, on gallbladder cancer both in vitro and in vivo and to explore the mechanisms underlying oridonin-induced apoptosis and cell cycle arrest. METHODS: The anti-tumor activity of oridonin on SGC996 and NOZ cells was assessed by the MTT and colony forming assays. Cell cycle changes were detected by flow cytometric analysis. Apoptosis was detected by annexin V/PI double-staining and Hoechst 33342 staining assays. Loss of mitochondrial membrane potential was observed by Rhodamine 123 staining. The in vivo efficacy of oridonin was evaluated using a NOZ xenograft model in athymic nude mice. The expression of cell cycle- and apoptosis-related proteins in vitro and in vivo was analyzed by western blot analysis. Activation of caspases (caspase-3, -8 and -9) was measured by caspases activity assay. RESULTS: Oridonin induced potent growth inhibition, S-phase arrest, apoptosis, and colony-forming inhibition in SGC996 and NOZ cells in a dose-dependent manner. Intraperitoneal injection of oridonin (5, 10, or 15 mg/kg) for 3 weeks significantly inhibited the growth of NOZ xenografts in athymic nude mice. We demonstrated that oridonin regulated cell cycle-related proteins in response to S-phase arrest by western blot analysis. In contrast, we observed inhibition of NF-κB nuclear translocation and an increase Bax/Bcl-2 ratio accompanied by activated caspase-3, caspase-9 and PARP-1 cleavage after treatment with oridonin, which indicate that the mitochondrial pathway is involved in oridonin-mediated apoptosis. CONCLUSIONS: Oridonin possesses potent anti-gallbladder cancer activities that correlate with regulation of the mitochondrial pathway, which is critical for apoptosis and S-phase arrest. Therefore, oridonin has potential as a novel anti-tumor therapy for the treatment of gallbladder cancer. |
format | Online Article Text |
id | pubmed-3994450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39944502014-04-23 Oridonin induces apoptosis and cell cycle arrest of gallbladder cancer cells via the mitochondrial pathway Bao, Runfa Shu, Yijun Wu, Xiangsong Weng, Hao Ding, Qian Cao, Yang Li, Maolan Mu, Jiasheng Wu, Wenguang Ding, Qichen Tan, Zhujun Liu, Tianyu Jiang, Lin Hu, Yunping Gu, Jianfeng Liu, Yingbin BMC Cancer Research Article BACKGROUND: Gallbladder cancer is the most frequent malignancy of the bile duct with high aggressive and extremely poor prognosis. The main objective of the paper was to investigate the inhibitory effects of oridonin, a diterpenoid isolated from Rabdosia rubescens, on gallbladder cancer both in vitro and in vivo and to explore the mechanisms underlying oridonin-induced apoptosis and cell cycle arrest. METHODS: The anti-tumor activity of oridonin on SGC996 and NOZ cells was assessed by the MTT and colony forming assays. Cell cycle changes were detected by flow cytometric analysis. Apoptosis was detected by annexin V/PI double-staining and Hoechst 33342 staining assays. Loss of mitochondrial membrane potential was observed by Rhodamine 123 staining. The in vivo efficacy of oridonin was evaluated using a NOZ xenograft model in athymic nude mice. The expression of cell cycle- and apoptosis-related proteins in vitro and in vivo was analyzed by western blot analysis. Activation of caspases (caspase-3, -8 and -9) was measured by caspases activity assay. RESULTS: Oridonin induced potent growth inhibition, S-phase arrest, apoptosis, and colony-forming inhibition in SGC996 and NOZ cells in a dose-dependent manner. Intraperitoneal injection of oridonin (5, 10, or 15 mg/kg) for 3 weeks significantly inhibited the growth of NOZ xenografts in athymic nude mice. We demonstrated that oridonin regulated cell cycle-related proteins in response to S-phase arrest by western blot analysis. In contrast, we observed inhibition of NF-κB nuclear translocation and an increase Bax/Bcl-2 ratio accompanied by activated caspase-3, caspase-9 and PARP-1 cleavage after treatment with oridonin, which indicate that the mitochondrial pathway is involved in oridonin-mediated apoptosis. CONCLUSIONS: Oridonin possesses potent anti-gallbladder cancer activities that correlate with regulation of the mitochondrial pathway, which is critical for apoptosis and S-phase arrest. Therefore, oridonin has potential as a novel anti-tumor therapy for the treatment of gallbladder cancer. BioMed Central 2014-03-21 /pmc/articles/PMC3994450/ /pubmed/24655726 http://dx.doi.org/10.1186/1471-2407-14-217 Text en Copyright © 2014 Bao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Bao, Runfa Shu, Yijun Wu, Xiangsong Weng, Hao Ding, Qian Cao, Yang Li, Maolan Mu, Jiasheng Wu, Wenguang Ding, Qichen Tan, Zhujun Liu, Tianyu Jiang, Lin Hu, Yunping Gu, Jianfeng Liu, Yingbin Oridonin induces apoptosis and cell cycle arrest of gallbladder cancer cells via the mitochondrial pathway |
title | Oridonin induces apoptosis and cell cycle arrest of gallbladder cancer cells via the mitochondrial pathway |
title_full | Oridonin induces apoptosis and cell cycle arrest of gallbladder cancer cells via the mitochondrial pathway |
title_fullStr | Oridonin induces apoptosis and cell cycle arrest of gallbladder cancer cells via the mitochondrial pathway |
title_full_unstemmed | Oridonin induces apoptosis and cell cycle arrest of gallbladder cancer cells via the mitochondrial pathway |
title_short | Oridonin induces apoptosis and cell cycle arrest of gallbladder cancer cells via the mitochondrial pathway |
title_sort | oridonin induces apoptosis and cell cycle arrest of gallbladder cancer cells via the mitochondrial pathway |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994450/ https://www.ncbi.nlm.nih.gov/pubmed/24655726 http://dx.doi.org/10.1186/1471-2407-14-217 |
work_keys_str_mv | AT baorunfa oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT shuyijun oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT wuxiangsong oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT wenghao oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT dingqian oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT caoyang oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT limaolan oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT mujiasheng oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT wuwenguang oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT dingqichen oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT tanzhujun oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT liutianyu oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT jianglin oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT huyunping oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT gujianfeng oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway AT liuyingbin oridonininducesapoptosisandcellcyclearrestofgallbladdercancercellsviathemitochondrialpathway |