Cargando…
4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of HMGB1, HIF1α and Caveolin-1
Metastasis is a great challenge in lung adenocarcinoma (ADC) therapy. Cholesterol has been implicated in ADC metastasis. 4-cholesten-3-one, as cholesterol metabolite and analog, can substitute membrane cholesterol and increase membrane fluidity. In this study, we explored the possibility that 4-chol...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059879/ https://www.ncbi.nlm.nih.gov/pubmed/27899819 http://dx.doi.org/10.1038/cddis.2016.281 |
_version_ | 1782459493216419840 |
---|---|
author | Ma, Jinben Fu, Guobin Wu, Jing Han, Shaoxian Zhang, Lishan Yang, Ming Yu, Yong Zhang, Mengyuan Lin, Yanliang Wang, Yibing |
author_facet | Ma, Jinben Fu, Guobin Wu, Jing Han, Shaoxian Zhang, Lishan Yang, Ming Yu, Yong Zhang, Mengyuan Lin, Yanliang Wang, Yibing |
author_sort | Ma, Jinben |
collection | PubMed |
description | Metastasis is a great challenge in lung adenocarcinoma (ADC) therapy. Cholesterol has been implicated in ADC metastasis. 4-cholesten-3-one, as cholesterol metabolite and analog, can substitute membrane cholesterol and increase membrane fluidity. In this study, we explored the possibility that 4-cholesten-3-one inhibited ADC metastasis. Low-dose 4-cholesten-3-one significantly restrained ADC cells migration and invasion with little effects on cells viabilities. Further investigation showed that 4-cholesten-3-one promoted ROS generation, which transiently activated AMPKα1, increased HIF1α expression, reduced Bcl-2 expression and caused autophagy. AMPKα1 knockdown partly suppressed 4-cholesten-3-one-induced autophagy but, neither prevented 4-cholesten-3-one-induced upregulation of HIF1α or downregulation of Bcl-2. 4-cholesten-3-one-induced autophagy facilitated the release of HMGB1 from nuclei to cytoplasm, blocking nuclear translocation of HIF1α and activation of MMP2 and MMP9. Also, 4-cholesten-3-one induced time-dependent phosphorylation of caveolin-1, Akt and NF-κB. With increasing treatment time, 4-cholesten-3-one accelerated caveolin-1 internalization, but reduced the phosphorylation of Akt and NF-κB, and inhibited the expression of snail and twist. These data suggested that 4-cholesten-3-one could be a potential candidate for anti-metastasis of lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-5059879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50598792016-10-26 4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of HMGB1, HIF1α and Caveolin-1 Ma, Jinben Fu, Guobin Wu, Jing Han, Shaoxian Zhang, Lishan Yang, Ming Yu, Yong Zhang, Mengyuan Lin, Yanliang Wang, Yibing Cell Death Dis Original Article Metastasis is a great challenge in lung adenocarcinoma (ADC) therapy. Cholesterol has been implicated in ADC metastasis. 4-cholesten-3-one, as cholesterol metabolite and analog, can substitute membrane cholesterol and increase membrane fluidity. In this study, we explored the possibility that 4-cholesten-3-one inhibited ADC metastasis. Low-dose 4-cholesten-3-one significantly restrained ADC cells migration and invasion with little effects on cells viabilities. Further investigation showed that 4-cholesten-3-one promoted ROS generation, which transiently activated AMPKα1, increased HIF1α expression, reduced Bcl-2 expression and caused autophagy. AMPKα1 knockdown partly suppressed 4-cholesten-3-one-induced autophagy but, neither prevented 4-cholesten-3-one-induced upregulation of HIF1α or downregulation of Bcl-2. 4-cholesten-3-one-induced autophagy facilitated the release of HMGB1 from nuclei to cytoplasm, blocking nuclear translocation of HIF1α and activation of MMP2 and MMP9. Also, 4-cholesten-3-one induced time-dependent phosphorylation of caveolin-1, Akt and NF-κB. With increasing treatment time, 4-cholesten-3-one accelerated caveolin-1 internalization, but reduced the phosphorylation of Akt and NF-κB, and inhibited the expression of snail and twist. These data suggested that 4-cholesten-3-one could be a potential candidate for anti-metastasis of lung adenocarcinoma. Nature Publishing Group 2016-09 2016-09-22 /pmc/articles/PMC5059879/ /pubmed/27899819 http://dx.doi.org/10.1038/cddis.2016.281 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Ma, Jinben Fu, Guobin Wu, Jing Han, Shaoxian Zhang, Lishan Yang, Ming Yu, Yong Zhang, Mengyuan Lin, Yanliang Wang, Yibing 4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of HMGB1, HIF1α and Caveolin-1 |
title | 4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of HMGB1, HIF1α and Caveolin-1 |
title_full | 4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of HMGB1, HIF1α and Caveolin-1 |
title_fullStr | 4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of HMGB1, HIF1α and Caveolin-1 |
title_full_unstemmed | 4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of HMGB1, HIF1α and Caveolin-1 |
title_short | 4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of HMGB1, HIF1α and Caveolin-1 |
title_sort | 4-cholesten-3-one suppresses lung adenocarcinoma metastasis by regulating translocation of hmgb1, hif1α and caveolin-1 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059879/ https://www.ncbi.nlm.nih.gov/pubmed/27899819 http://dx.doi.org/10.1038/cddis.2016.281 |
work_keys_str_mv | AT majinben 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 AT fuguobin 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 AT wujing 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 AT hanshaoxian 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 AT zhanglishan 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 AT yangming 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 AT yuyong 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 AT zhangmengyuan 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 AT linyanliang 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 AT wangyibing 4cholesten3onesuppresseslungadenocarcinomametastasisbyregulatingtranslocationofhmgb1hif1aandcaveolin1 |