Oxidative stress in NSC-741909-induced apoptosis of cancer cells

<p>Abstract</p> <p>Background</p> <p>NSC-741909 is a novel anticancer agent that can effectively suppress the growth of several cell lines derived from lung, colon, breast, ovarian, and kidney cancers. We recently showed that NSC-741909-induced antitumor activity is ass...

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Main Authors: Huang Peng, Wang Li, Wu Shuhong, Guo Wei, Wei Xiaoli, Liu Jinsong, Fang Bingliang
Format: Article
Language:English
Published: BMC 2010-04-01
Series:Journal of Translational Medicine
Online Access:http://www.translational-medicine.com/content/8/1/37
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author Huang Peng
Wang Li
Wu Shuhong
Guo Wei
Wei Xiaoli
Liu Jinsong
Fang Bingliang
author_facet Huang Peng
Wang Li
Wu Shuhong
Guo Wei
Wei Xiaoli
Liu Jinsong
Fang Bingliang
author_sort Huang Peng
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>NSC-741909 is a novel anticancer agent that can effectively suppress the growth of several cell lines derived from lung, colon, breast, ovarian, and kidney cancers. We recently showed that NSC-741909-induced antitumor activity is associated with sustained Jun N-terminal kinase (JNK) activation, resulting from suppression of JNK dephosphorylation associated with decreased protein levels of MAPK phosphatase-1. However, the mechanisms of NSC-741909-induced antitumor activity remain unclear. Because JNK is frequently activated by oxidative stress in cells, we hypothesized that reactive oxygen species (ROS) may be involved in the suppression of JNK dephosphorylation and the cytotoxicity of NSC-741909.</p> <p>Methods</p> <p>The generation of ROS was measured by using the cell-permeable nonfluorescent compound H<sub>2</sub>DCF-DA and flow cytometry analysis. Cell viability was determined by sulforhodamine B assay. Western blot analysis, immunofluorescent staining and flow cytometry assays were used to determine apoptosis and molecular changes induced by NSC-741909.</p> <p>Results</p> <p>Treatment with NSC-741909 induced robust ROS generation and marked MAPK phosphatase-1 and -7 clustering in NSC-741909-sensitive, but not resistant cell lines, in a dose- and time-dependent manner. The generation of ROS was detectable as early as 30 min and ROS levels were as high as 6- to 8-fold above basal levels after treatment. Moreover, the NSC-741909-induced ROS generation could be blocked by pretreatment with antioxidants, such as nordihydroguaiaretic acid, aesculetin, baicalein, and caffeic acid, which in turn, inhibited the NSC-741909-induced JNK activation and apoptosis.</p> <p>Conclusion</p> <p>Our results demonstrate that the increased ROS production was associated with NSC-741909-induced antitumor activity and that ROS generation and subsequent JNK activation is one of the primary mechanisms of NSC-741909-mediated antitumor cell activity.</p>
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spelling doaj.art-0b366837697d4642bb2d05d5c64e8f112022-12-22T03:01:23ZengBMCJournal of Translational Medicine1479-58762010-04-01813710.1186/1479-5876-8-37Oxidative stress in NSC-741909-induced apoptosis of cancer cellsHuang PengWang LiWu ShuhongGuo WeiWei XiaoliLiu JinsongFang Bingliang<p>Abstract</p> <p>Background</p> <p>NSC-741909 is a novel anticancer agent that can effectively suppress the growth of several cell lines derived from lung, colon, breast, ovarian, and kidney cancers. We recently showed that NSC-741909-induced antitumor activity is associated with sustained Jun N-terminal kinase (JNK) activation, resulting from suppression of JNK dephosphorylation associated with decreased protein levels of MAPK phosphatase-1. However, the mechanisms of NSC-741909-induced antitumor activity remain unclear. Because JNK is frequently activated by oxidative stress in cells, we hypothesized that reactive oxygen species (ROS) may be involved in the suppression of JNK dephosphorylation and the cytotoxicity of NSC-741909.</p> <p>Methods</p> <p>The generation of ROS was measured by using the cell-permeable nonfluorescent compound H<sub>2</sub>DCF-DA and flow cytometry analysis. Cell viability was determined by sulforhodamine B assay. Western blot analysis, immunofluorescent staining and flow cytometry assays were used to determine apoptosis and molecular changes induced by NSC-741909.</p> <p>Results</p> <p>Treatment with NSC-741909 induced robust ROS generation and marked MAPK phosphatase-1 and -7 clustering in NSC-741909-sensitive, but not resistant cell lines, in a dose- and time-dependent manner. The generation of ROS was detectable as early as 30 min and ROS levels were as high as 6- to 8-fold above basal levels after treatment. Moreover, the NSC-741909-induced ROS generation could be blocked by pretreatment with antioxidants, such as nordihydroguaiaretic acid, aesculetin, baicalein, and caffeic acid, which in turn, inhibited the NSC-741909-induced JNK activation and apoptosis.</p> <p>Conclusion</p> <p>Our results demonstrate that the increased ROS production was associated with NSC-741909-induced antitumor activity and that ROS generation and subsequent JNK activation is one of the primary mechanisms of NSC-741909-mediated antitumor cell activity.</p>http://www.translational-medicine.com/content/8/1/37
spellingShingle Huang Peng
Wang Li
Wu Shuhong
Guo Wei
Wei Xiaoli
Liu Jinsong
Fang Bingliang
Oxidative stress in NSC-741909-induced apoptosis of cancer cells
Journal of Translational Medicine
title Oxidative stress in NSC-741909-induced apoptosis of cancer cells
title_full Oxidative stress in NSC-741909-induced apoptosis of cancer cells
title_fullStr Oxidative stress in NSC-741909-induced apoptosis of cancer cells
title_full_unstemmed Oxidative stress in NSC-741909-induced apoptosis of cancer cells
title_short Oxidative stress in NSC-741909-induced apoptosis of cancer cells
title_sort oxidative stress in nsc 741909 induced apoptosis of cancer cells
url http://www.translational-medicine.com/content/8/1/37
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AT wangli oxidativestressinnsc741909inducedapoptosisofcancercells
AT wushuhong oxidativestressinnsc741909inducedapoptosisofcancercells
AT guowei oxidativestressinnsc741909inducedapoptosisofcancercells
AT weixiaoli oxidativestressinnsc741909inducedapoptosisofcancercells
AT liujinsong oxidativestressinnsc741909inducedapoptosisofcancercells
AT fangbingliang oxidativestressinnsc741909inducedapoptosisofcancercells