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Introducing the Role of Genotoxicity in Neurodegenerative Diseases and Neuropsychiatric Disorders
被引:2
|作者:
Kisby, Glen E.
[1
]
Wilson, David M.
[2
]
Spencer, Peter S.
[3
]
机构:
[1] Western Univ Hlth Sci, Coll Osteopath Med Pacific Northwest, Dept Biomed Sci, Lebanon, OR 97355 USA
[2] Hasselt Univ, Biomed Res Inst, BIOMED, B-3500 Hasselt, Belgium
[3] Oregon Hlth & Sci Univ OHSU, Oregon Inst Occupat Hlth Sci, Sch Med, Dept Neurol, Portland, OR 97239 USA
关键词:
genomic instability;
genomic stress;
DNA damage response (DDR);
DNA repair;
environment;
AMYOTROPHIC-LATERAL-SCLEROSIS;
DNA-DAMAGE RESPONSE;
DIAGNOSED BIPOLAR DISORDER;
BASE EXCISION-REPAIR;
OXIDATIVE STRESS;
PARKINSONISM-DEMENTIA;
ALZHEIMERS-DISEASE;
AGRICULTURAL-WORKERS;
COCKAYNE-SYNDROME;
STRAND BREAKS;
D O I:
10.3390/ijms25137221
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:
Decades of research have identified genetic and environmental factors involved in age-related neurodegenerative diseases and, to a lesser extent, neuropsychiatric disorders. Genomic instability, i.e., the loss of genome integrity, is a common feature among both neurodegenerative (mayo-trophic lateral sclerosis, Parkinson's disease, Alzheimer's disease) and psychiatric (schizophrenia, autism, bipolar depression) disorders. Genomic instability is associated with the accumulation of persistent DNA damage and the activation of DNA damage response (DDR) pathways, as well as pathologic neuronal cell loss or senescence. Typically, DDR signaling ensures that genomic and proteomic homeostasis are maintained in both dividing cells, including neural progenitors, and post-mitotic neurons. However, dysregulation of these protective responses, in part due to aging or environmental insults, contributes to the progressive development of neurodegenerative and/or psychiatric disorders. In this Special Issue, we introduce and highlight the overlap between neurodegenerative diseases and neuropsychiatric disorders, as well as the emerging clinical, genomic, and molecular evidence for the contributions of DNA damage and aberrant DNA repair. Our goal is to illuminate the importance of this subject to uncover possible treatment and prevention strategies for relevant devastating brain diseases.
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