Pterostilbene exerts anticancer activity on non-small-cell lung cancer via activating endoplasmic reticulum stress
Abstract Pterostilbene (PT), the natural dimethylated analog of resveratrol (RSV), is a potent anticarcinogen for non-small-cell lung cancer (NSCLC), but its anti-NSCLC mechanisms remain unclear. In this study, we show that PT treatment time- and dose-dependently enhanced the endoplasmic reticulum s...
Guardado en:
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/2659c22ced554d26bcb696a3b90b514b |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:2659c22ced554d26bcb696a3b90b514b |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:2659c22ced554d26bcb696a3b90b514b2021-12-02T16:08:24ZPterostilbene exerts anticancer activity on non-small-cell lung cancer via activating endoplasmic reticulum stress10.1038/s41598-017-08547-02045-2322https://doaj.org/article/2659c22ced554d26bcb696a3b90b514b2017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-08547-0https://doaj.org/toc/2045-2322Abstract Pterostilbene (PT), the natural dimethylated analog of resveratrol (RSV), is a potent anticarcinogen for non-small-cell lung cancer (NSCLC), but its anti-NSCLC mechanisms remain unclear. In this study, we show that PT treatment time- and dose-dependently enhanced the endoplasmic reticulum stress (ERS) signaling (i.e., p-PERK, IRE1, ATF4, CHOP), thus decreasing the cell viability and inducing apoptosis in human PC9 and A549 NSCLC cell lines. Moreover, the decreased migratory and adhesive abilities, downregulation of intracellular glutathione (GSH) level, enhanced reactive oxygen species (ROS) generation, Caspase 3 activity and mitochondrial membrane depolarization were observed in NSCLC cells treated with PT. These effects were reversed by CHOP siRNA which inhibited the ERS signaling pathway, but were promoted by thapsigargin (a classical ERS inducer) in vitro. Besides, in vivo studies also verify that PT exerted anticancer activity by mobilizing ERS signaling and apoptosis-related proteins, and these effects were enhanced by thapsigargin. Therefore, ERS activation may represent a new mechanism of anti-NSCLC action by PT, and a novel therapeutic intervention for lung cancer.Zhiqiang MaYang YangShouyin DiXiao FengDong LiuShuai JiangWei HuZhigang QinYue LiJianjun LvChongxi FanXiaolong YanXiaofei LiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-14 (2017) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Zhiqiang Ma Yang Yang Shouyin Di Xiao Feng Dong Liu Shuai Jiang Wei Hu Zhigang Qin Yue Li Jianjun Lv Chongxi Fan Xiaolong Yan Xiaofei Li Pterostilbene exerts anticancer activity on non-small-cell lung cancer via activating endoplasmic reticulum stress |
description |
Abstract Pterostilbene (PT), the natural dimethylated analog of resveratrol (RSV), is a potent anticarcinogen for non-small-cell lung cancer (NSCLC), but its anti-NSCLC mechanisms remain unclear. In this study, we show that PT treatment time- and dose-dependently enhanced the endoplasmic reticulum stress (ERS) signaling (i.e., p-PERK, IRE1, ATF4, CHOP), thus decreasing the cell viability and inducing apoptosis in human PC9 and A549 NSCLC cell lines. Moreover, the decreased migratory and adhesive abilities, downregulation of intracellular glutathione (GSH) level, enhanced reactive oxygen species (ROS) generation, Caspase 3 activity and mitochondrial membrane depolarization were observed in NSCLC cells treated with PT. These effects were reversed by CHOP siRNA which inhibited the ERS signaling pathway, but were promoted by thapsigargin (a classical ERS inducer) in vitro. Besides, in vivo studies also verify that PT exerted anticancer activity by mobilizing ERS signaling and apoptosis-related proteins, and these effects were enhanced by thapsigargin. Therefore, ERS activation may represent a new mechanism of anti-NSCLC action by PT, and a novel therapeutic intervention for lung cancer. |
format |
article |
author |
Zhiqiang Ma Yang Yang Shouyin Di Xiao Feng Dong Liu Shuai Jiang Wei Hu Zhigang Qin Yue Li Jianjun Lv Chongxi Fan Xiaolong Yan Xiaofei Li |
author_facet |
Zhiqiang Ma Yang Yang Shouyin Di Xiao Feng Dong Liu Shuai Jiang Wei Hu Zhigang Qin Yue Li Jianjun Lv Chongxi Fan Xiaolong Yan Xiaofei Li |
author_sort |
Zhiqiang Ma |
title |
Pterostilbene exerts anticancer activity on non-small-cell lung cancer via activating endoplasmic reticulum stress |
title_short |
Pterostilbene exerts anticancer activity on non-small-cell lung cancer via activating endoplasmic reticulum stress |
title_full |
Pterostilbene exerts anticancer activity on non-small-cell lung cancer via activating endoplasmic reticulum stress |
title_fullStr |
Pterostilbene exerts anticancer activity on non-small-cell lung cancer via activating endoplasmic reticulum stress |
title_full_unstemmed |
Pterostilbene exerts anticancer activity on non-small-cell lung cancer via activating endoplasmic reticulum stress |
title_sort |
pterostilbene exerts anticancer activity on non-small-cell lung cancer via activating endoplasmic reticulum stress |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/2659c22ced554d26bcb696a3b90b514b |
work_keys_str_mv |
AT zhiqiangma pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT yangyang pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT shouyindi pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT xiaofeng pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT dongliu pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT shuaijiang pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT weihu pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT zhigangqin pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT yueli pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT jianjunlv pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT chongxifan pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT xiaolongyan pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress AT xiaofeili pterostilbeneexertsanticanceractivityonnonsmallcelllungcancerviaactivatingendoplasmicreticulumstress |
_version_ |
1718384518119817216 |