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Androgens induce oxidative stress and radiation resistance in prostate cancer cells though NADPH oxidase
Androgen deprivation therapy (ADT) facilitates the response of prostate cancer (PC) to radiation. Androgens have been shown to induce elevated basal levels of reactive oxygen species (ROS) in PC, leading to adaptation to radiation-induced cytotoxic oxidative stress. Here, we show that androgens incr...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834342/ https://www.ncbi.nlm.nih.gov/pubmed/19546883 http://dx.doi.org/10.1038/pcan.2009.24 |
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author | Lu, J P Monardo, L Bryskin, I Hou, Z F Trachtenberg, J Wilson, B C Pinthus, J H |
author_facet | Lu, J P Monardo, L Bryskin, I Hou, Z F Trachtenberg, J Wilson, B C Pinthus, J H |
author_sort | Lu, J P |
collection | PubMed |
description | Androgen deprivation therapy (ADT) facilitates the response of prostate cancer (PC) to radiation. Androgens have been shown to induce elevated basal levels of reactive oxygen species (ROS) in PC, leading to adaptation to radiation-induced cytotoxic oxidative stress. Here, we show that androgens increase the expression of p22(phox) and gp91(phox) subunits of NADPH oxidase (NOX) and ROS production by NOX2 and NOX4 in PC. Pre-radiation treatment of 22Rv1 human PC cells with NOX inhibitors sensitize the cells to radiation similarly to ADT, suggesting that their future usage may spare the need for adjuvant ADT in PC patients undergoing radiation. |
format | Text |
id | pubmed-2834342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-28343422010-03-29 Androgens induce oxidative stress and radiation resistance in prostate cancer cells though NADPH oxidase Lu, J P Monardo, L Bryskin, I Hou, Z F Trachtenberg, J Wilson, B C Pinthus, J H Prostate Cancer Prostatic Dis Original Articles Androgen deprivation therapy (ADT) facilitates the response of prostate cancer (PC) to radiation. Androgens have been shown to induce elevated basal levels of reactive oxygen species (ROS) in PC, leading to adaptation to radiation-induced cytotoxic oxidative stress. Here, we show that androgens increase the expression of p22(phox) and gp91(phox) subunits of NADPH oxidase (NOX) and ROS production by NOX2 and NOX4 in PC. Pre-radiation treatment of 22Rv1 human PC cells with NOX inhibitors sensitize the cells to radiation similarly to ADT, suggesting that their future usage may spare the need for adjuvant ADT in PC patients undergoing radiation. Nature Publishing Group 2009-06-23 2010-03 /pmc/articles/PMC2834342/ /pubmed/19546883 http://dx.doi.org/10.1038/pcan.2009.24 Text en Copyright 2010, Nature Publishing Group http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Original Articles Lu, J P Monardo, L Bryskin, I Hou, Z F Trachtenberg, J Wilson, B C Pinthus, J H Androgens induce oxidative stress and radiation resistance in prostate cancer cells though NADPH oxidase |
title | Androgens induce oxidative stress and radiation resistance in prostate cancer cells though NADPH oxidase |
title_full | Androgens induce oxidative stress and radiation resistance in prostate cancer cells though NADPH oxidase |
title_fullStr | Androgens induce oxidative stress and radiation resistance in prostate cancer cells though NADPH oxidase |
title_full_unstemmed | Androgens induce oxidative stress and radiation resistance in prostate cancer cells though NADPH oxidase |
title_short | Androgens induce oxidative stress and radiation resistance in prostate cancer cells though NADPH oxidase |
title_sort | androgens induce oxidative stress and radiation resistance in prostate cancer cells though nadph oxidase |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834342/ https://www.ncbi.nlm.nih.gov/pubmed/19546883 http://dx.doi.org/10.1038/pcan.2009.24 |
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