Cargando…

6-Gingerol suppresses cell viability, migration and invasion via inhibiting EMT, and inducing autophagy and ferroptosis in LPS-stimulated and LPS-unstimulated prostate cancer cells

6-Gingerol is a bioactive compound isolated from Zingiber officinale. 6-Gingerol has been shown to have anticancer effects in numerous types of cancer cell. The mechanisms underlying the anticancer effect of 6-Gingerol in prostate cancer requires investigation. In the present study, the effect on ce...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Chi-Ming, An, Lijie, Wu, Zhengping, Ouyang, Ai-Jun, Su, Mengqiao, Shao, Zichen, Lin, Yi, Liu, Xiaoyu, Jiang, Yinjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073581/
https://www.ncbi.nlm.nih.gov/pubmed/35527779
http://dx.doi.org/10.3892/ol.2022.13307
_version_ 1784701319918911488
author Liu, Chi-Ming
An, Lijie
Wu, Zhengping
Ouyang, Ai-Jun
Su, Mengqiao
Shao, Zichen
Lin, Yi
Liu, Xiaoyu
Jiang, Yinjie
author_facet Liu, Chi-Ming
An, Lijie
Wu, Zhengping
Ouyang, Ai-Jun
Su, Mengqiao
Shao, Zichen
Lin, Yi
Liu, Xiaoyu
Jiang, Yinjie
author_sort Liu, Chi-Ming
collection PubMed
description 6-Gingerol is a bioactive compound isolated from Zingiber officinale. 6-Gingerol has been shown to have anticancer effects in numerous types of cancer cell. The mechanisms underlying the anticancer effect of 6-Gingerol in prostate cancer requires investigation. In the present study, the effect on cell viability of 6-Gingerol on LNCaP, PC3 and DU145 prostate cancer cells were determined using the MTT and colony formation assays. 6-Gingerol significantly inhibited cell migration, adhesion and invasion in LPS-stimulated and LPS-unstimulated prostate cancer cells. Furthermore, these changes were accompanied by alterations in the protein expression levels of epithelial-mesenchymal transition biomarkers, including E-cadherin, N-cadherin, Vimentin and zonula occludens-1. 6-Gingerol also induced autophagy by significantly increasing LC3B-II and Beclin-1 protein expression levels in prostate cancer cells. Combining 6-Gingerol with LY294002, an autophagy inhibitor, significantly increased cell survival in DU145 cells. Furthermore, 6-Gingerol significantly decreased the protein expression levels of glutathione (GSH) peroxidase 4 and nuclear factor erythroid 2-related factor 2 in prostate cancer cells. Reactive oxygen species (ROS) levels were significantly increased but GSH levels were decreased following 6-Gingerol treatment in prostate cancer cells. Co-treatment with the ferroptosis inhibitor, ferrostatin-1, significantly increased cell viability and significantly decreased ROS levels in 6-Gingerol-treated cells. These results suggested that 6-Gingerol may have inhibited prostate cell cancer viability via the regulation of autophagy and ferroptosis. In addition, 6-Gingerol inhibited cell migration, adhesion and invasion via the regulation of EMT-related protein expression levels in LPS-stimulated and LPS-unstimulated prostate cancer cells. In conclusion, 6-Gingerol may induce protective autophagy, autophagic cell death and ferroptosis-mediated cell death in prostate cancer cells. These findings may provide a strategy for the treatment and prevention of prostate cancer.
format Online
Article
Text
id pubmed-9073581
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-90735812022-05-07 6-Gingerol suppresses cell viability, migration and invasion via inhibiting EMT, and inducing autophagy and ferroptosis in LPS-stimulated and LPS-unstimulated prostate cancer cells Liu, Chi-Ming An, Lijie Wu, Zhengping Ouyang, Ai-Jun Su, Mengqiao Shao, Zichen Lin, Yi Liu, Xiaoyu Jiang, Yinjie Oncol Lett Articles 6-Gingerol is a bioactive compound isolated from Zingiber officinale. 6-Gingerol has been shown to have anticancer effects in numerous types of cancer cell. The mechanisms underlying the anticancer effect of 6-Gingerol in prostate cancer requires investigation. In the present study, the effect on cell viability of 6-Gingerol on LNCaP, PC3 and DU145 prostate cancer cells were determined using the MTT and colony formation assays. 6-Gingerol significantly inhibited cell migration, adhesion and invasion in LPS-stimulated and LPS-unstimulated prostate cancer cells. Furthermore, these changes were accompanied by alterations in the protein expression levels of epithelial-mesenchymal transition biomarkers, including E-cadherin, N-cadherin, Vimentin and zonula occludens-1. 6-Gingerol also induced autophagy by significantly increasing LC3B-II and Beclin-1 protein expression levels in prostate cancer cells. Combining 6-Gingerol with LY294002, an autophagy inhibitor, significantly increased cell survival in DU145 cells. Furthermore, 6-Gingerol significantly decreased the protein expression levels of glutathione (GSH) peroxidase 4 and nuclear factor erythroid 2-related factor 2 in prostate cancer cells. Reactive oxygen species (ROS) levels were significantly increased but GSH levels were decreased following 6-Gingerol treatment in prostate cancer cells. Co-treatment with the ferroptosis inhibitor, ferrostatin-1, significantly increased cell viability and significantly decreased ROS levels in 6-Gingerol-treated cells. These results suggested that 6-Gingerol may have inhibited prostate cell cancer viability via the regulation of autophagy and ferroptosis. In addition, 6-Gingerol inhibited cell migration, adhesion and invasion via the regulation of EMT-related protein expression levels in LPS-stimulated and LPS-unstimulated prostate cancer cells. In conclusion, 6-Gingerol may induce protective autophagy, autophagic cell death and ferroptosis-mediated cell death in prostate cancer cells. These findings may provide a strategy for the treatment and prevention of prostate cancer. D.A. Spandidos 2022-06 2022-04-26 /pmc/articles/PMC9073581/ /pubmed/35527779 http://dx.doi.org/10.3892/ol.2022.13307 Text en Copyright: © Liu et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Liu, Chi-Ming
An, Lijie
Wu, Zhengping
Ouyang, Ai-Jun
Su, Mengqiao
Shao, Zichen
Lin, Yi
Liu, Xiaoyu
Jiang, Yinjie
6-Gingerol suppresses cell viability, migration and invasion via inhibiting EMT, and inducing autophagy and ferroptosis in LPS-stimulated and LPS-unstimulated prostate cancer cells
title 6-Gingerol suppresses cell viability, migration and invasion via inhibiting EMT, and inducing autophagy and ferroptosis in LPS-stimulated and LPS-unstimulated prostate cancer cells
title_full 6-Gingerol suppresses cell viability, migration and invasion via inhibiting EMT, and inducing autophagy and ferroptosis in LPS-stimulated and LPS-unstimulated prostate cancer cells
title_fullStr 6-Gingerol suppresses cell viability, migration and invasion via inhibiting EMT, and inducing autophagy and ferroptosis in LPS-stimulated and LPS-unstimulated prostate cancer cells
title_full_unstemmed 6-Gingerol suppresses cell viability, migration and invasion via inhibiting EMT, and inducing autophagy and ferroptosis in LPS-stimulated and LPS-unstimulated prostate cancer cells
title_short 6-Gingerol suppresses cell viability, migration and invasion via inhibiting EMT, and inducing autophagy and ferroptosis in LPS-stimulated and LPS-unstimulated prostate cancer cells
title_sort 6-gingerol suppresses cell viability, migration and invasion via inhibiting emt, and inducing autophagy and ferroptosis in lps-stimulated and lps-unstimulated prostate cancer cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073581/
https://www.ncbi.nlm.nih.gov/pubmed/35527779
http://dx.doi.org/10.3892/ol.2022.13307
work_keys_str_mv AT liuchiming 6gingerolsuppressescellviabilitymigrationandinvasionviainhibitingemtandinducingautophagyandferroptosisinlpsstimulatedandlpsunstimulatedprostatecancercells
AT anlijie 6gingerolsuppressescellviabilitymigrationandinvasionviainhibitingemtandinducingautophagyandferroptosisinlpsstimulatedandlpsunstimulatedprostatecancercells
AT wuzhengping 6gingerolsuppressescellviabilitymigrationandinvasionviainhibitingemtandinducingautophagyandferroptosisinlpsstimulatedandlpsunstimulatedprostatecancercells
AT ouyangaijun 6gingerolsuppressescellviabilitymigrationandinvasionviainhibitingemtandinducingautophagyandferroptosisinlpsstimulatedandlpsunstimulatedprostatecancercells
AT sumengqiao 6gingerolsuppressescellviabilitymigrationandinvasionviainhibitingemtandinducingautophagyandferroptosisinlpsstimulatedandlpsunstimulatedprostatecancercells
AT shaozichen 6gingerolsuppressescellviabilitymigrationandinvasionviainhibitingemtandinducingautophagyandferroptosisinlpsstimulatedandlpsunstimulatedprostatecancercells
AT linyi 6gingerolsuppressescellviabilitymigrationandinvasionviainhibitingemtandinducingautophagyandferroptosisinlpsstimulatedandlpsunstimulatedprostatecancercells
AT liuxiaoyu 6gingerolsuppressescellviabilitymigrationandinvasionviainhibitingemtandinducingautophagyandferroptosisinlpsstimulatedandlpsunstimulatedprostatecancercells
AT jiangyinjie 6gingerolsuppressescellviabilitymigrationandinvasionviainhibitingemtandinducingautophagyandferroptosisinlpsstimulatedandlpsunstimulatedprostatecancercells