Reduction–oxidation (redox) system in radiation-induced normal tissue injury: molecular mechanisms and implications in radiation therapeutics

被引:0
作者
R. Yahyapour
E. Motevaseli
A. Rezaeyan
H. Abdollahi
B. Farhood
M. Cheki
S. Rezapoor
D. Shabeeb
A. E. Musa
M. Najafi
V. Villa
机构
[1] Jiroft University of Medical Sciences,School of Medicine
[2] Tehran University of Medical Sciences,Department of Molecular Medicine, School of Advanced Technologies in Medicine
[3] Iran University of Medical Sciences,Department of Medical Physics, School of Medicine
[4] Kashan University of Medical Sciences,Departments of Medical Physics and Radiology, Faculty of Paramedical Sciences
[5] Ahvaz Jundishapur University of Medical Sciences,Department of Radiologic Technology, Faculty of Paramedicine
[6] Tehran University of Medical Sciences,Department of Radiology, Faculty of Paramedical
[7] Tehran University of Medical Sciences,Department of Medical Physics and Biomedical Engineering, Faculty of Medicine
[8] University of Misan,Department of Physiology, College of Medicine
[9] Tehran University of Medical Sciences,Research Center for Molecular and Cellular Imaging
[10] Kermanshah University of Medical Science,Radiology and Nuclear Medicine Department, School of Paramedical Sciences
[11] Uniformed Services University of Health Sciences (USUHS),Scientific Research Department, Armed Forces Radiobiology Research Institute (AFRRI)
来源
Clinical and Translational Oncology | 2018年 / 20卷
关键词
Radiation; Redox; Normal tissue injury; Inflammation; NADPH oxidase;
D O I
暂无
中图分类号
学科分类号
摘要
Every year, millions of cancer patients undergo radiation therapy for treating and destroying abnormal cell growths within normal cell environmental conditions. Thus, ionizing radiation can have positive therapeutic effects on cancer cells as well as post-detrimental effects on surrounding normal tissues. Previous studies in the past years have proposed that the reduction and oxidation metabolism in cells changes in response to ionizing radiation and has a key role in radiation toxicity to normal tissue. Free radicals generated from ionizing radiation result in upregulation of cyclooxygenases (COXs), nitric oxide synthase (NOSs), lipoxygenases (LOXs) as well as nicotinamide adenine dinucleotide phosphate oxidase (NADPH oxidase), and their effected changes in mitochondrial functions are markedly noticeable. Each of these enzymes is diversely expressed in multiple cells, tissues and organs in a specific manner. Overproduction of reactive oxygen radicals (ROS), reactive hydroxyl radical (ROH) and reactive nitrogen radicals (RNS) in multiple cellular environments in the affected nucleus, cell membranes, cytosol and mitochondria, and other organelles, can specifically affect the sensitive and modifying enzymes of the redox system and repair proteins that play a pivotal role in both early and late effects of radiation. In recent years, ionizing radiation has been known to affect the redox functions and metabolism of NADPH oxidases (NOXs) as well as having destabilizing and detrimental effects on directly and indirectly affected cells, tissues and organs. More noteworthy, chronic free radical production may continue for years, increasing the risk of carcinogenesis and other oxidative stress-driven degenerative diseases as well as pathologies, in addition to late effect complications of organ fibrosis. Hence, knowledge about the mechanisms of chronic oxidative damage and injury in affected cells, tissues and organs following exposure to ionizing radiation may help in the development of treatment and management strategies of complications associated with radiotherapy (RT) or radiation accident victims. Thus, this medically relevant phenomenon may lead to the discovery of potential antioxidants and inhibitors with promising results in targeting and modulating the ROS/NO-sensitive enzymes in irradiated tissues and organ injury systems.
引用
收藏
页码:975 / 988
页数:13
相关论文
共 663 条
[1]  
Siegel RL(2017)Cancer statistics, 2017 CA Cancer J Clin 67 7-30
[2]  
Miller KD(2002)Major radiation exposure—what to expect and how to respond N Engl J Med 346 1554-1561
[3]  
Jemal A(2004)Radiation risks and dirty bombs Health Phys 86 S42-S47
[4]  
Mettler FA(2006)Radiation-induced bystander effects and the DNA paradigm: an “out of field” perspective Mutat Res 597 5-10
[5]  
Voelz GL(2004)Metabolic oxidation/reduction reactions and cellular responses to ionizing radiation: a unifying concept in stress response biology Cancer Metastasis Rev 23 311-322
[6]  
Ring JP(2009)High-dose selenium for the mitigation of radiation injury: a pilot study in a rat model Radiat Res 171 368-373
[7]  
Mothersill C(2009)Inflammation and chronic oxidative stress in radiation-induced late normal tissue injury: therapeutic implications Curr Med Chem 16 130-143
[8]  
Seymour CB(2017)The melatonin immunomodulatory actions in radiotherapy Biophys Rev 9 139-148
[9]  
Spitz DR(2011)Regulation of reactive oxygen species generation in cell signaling Mol Cells 32 491-509
[10]  
Azzam EI(2012)Oxidative stress and antioxidant defense World Allergy Organ J 5 9-19