Monogenic Disorders of ROS Production and the Primary Anti-Oxidative Defense

被引:6
|
作者
Gruening, Nana-Maria [1 ]
Ralser, Markus [1 ,2 ,3 ]
机构
[1] Charite Univ Med Berlin, Dept Biochem, D-10117 Berlin, Germany
[2] Univ Oxford, Wellcome Ctr Human Genet, Nuffield Dept Med, Oxford OX3 7BN, England
[3] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
关键词
oxidative stress; reactive oxygen species (ROS); cellular redox balance; monogenic disorder; inherited disease; DEHYDROGENASE-METHENYLTETRAHYDROFOLATE CYCLOHYDROLASE; CHRONIC GRANULOMATOUS-DISEASE; EARLY EMBRYONIC LETHALITY; MITOCHONDRIAL COMPLEX II; NITRIC-OXIDE SYNTHASE; OXIDATIVE STRESS; GLUTATHIONE-REDUCTASE; SYNTHETASE DEFICIENCY; HUMAN-BLOOD; MYELOPEROXIDASE DEFICIENCY;
D O I
10.3390/biom14020206
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
Oxidative stress, characterized by an imbalance between the production of reactive oxygen species (ROS) and the cellular anti-oxidant defense mechanisms, plays a critical role in the pathogenesis of various human diseases. Redox metabolism, comprising a network of enzymes and genes, serves as a crucial regulator of ROS levels and maintains cellular homeostasis. This review provides an overview of the most important human genes encoding for proteins involved in ROS generation, ROS detoxification, and production of reduced nicotinamide adenine dinucleotide phosphate (NADPH), and the genetic disorders that lead to dysregulation of these vital processes. Insights gained from studies on inherited monogenic metabolic diseases provide valuable basic understanding of redox metabolism and signaling, and they also help to unravel the underlying pathomechanisms that contribute to prevalent chronic disorders like cardiovascular disease, neurodegeneration, and cancer.
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页数:19
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