Regulation of apoptosis-related genes by nitric oxide in cancer

被引:51
|
作者
Olson, Samuel Y. [1 ]
Garban, Hermes J. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Div Surg Oncol, Dept Surg, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2008年 / 19卷 / 02期
关键词
nitric oxide; reactive nitrogen species; transcriptional regulation; gene expression; transcription factors; apoptosis; S-nitrosylation; YY1; NF-kappa B; p53; FOXP3;
D O I
10.1016/j.niox.2008.04.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nitric oxide (NO) is a simple molecule with a complex and pleiotropic biological activity. NO or related species have been implicated in the regulation of many genes that participate in many diverse biological functions including programmed cell death or apoptosis. Apoptosis is a process that may potentially be disrupted in cancer cells conferring a survival advantage. In addition, malignant tumor cells can develop an intricate system of resistance to apoptotic stimuli. NO or related species have been shown to play a dual role in the regulation of apoptosis in malignant cells either promoting cell death or protecting cells from pro-apoptotic induction. However, the specific role of NO in the regulation of apoptosis/survival-related genes expression seems to tilt the balance toward the promotion of pro-apoptotic and the suppression of anti-apoptotic genes. Herein we have reviewed the most relevant aspects involving NO and/or reactive intermediates in,the regulation of apoptosis-related genes-mainly-at the transcriptional level. We described the basic apoptotic molecules that potentially are affected by NO and how NO-mediated signaling gets transmitted to the transcriptional machinery that governs the expression of these genes. In addition, we discussed some of the fundamental functional consequences of the regulation of apoptosis-related genes by NO in cancer biology and its potential therapeutic implications. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:170 / 176
页数:7
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