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介绍遗传毒性在神经退行性疾病和神经精神障碍中的作用。

Introducing the Role of Genotoxicity in Neurodegenerative Diseases and Neuropsychiatric Disorders.

机构信息

Department of Biomedical Sciences, College of Osteopathic Medicine of Pacific Northwest, Western University of Health Sciences, Lebanon, OR 97355, USA.

Biomedical Research Institute, BIOMED, Hasselt University, 3500 Hasselt, Belgium.

出版信息

Int J Mol Sci. 2024 Jun 29;25(13):7221. doi: 10.3390/ijms25137221.


DOI:10.3390/ijms25137221
PMID:39000326
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11241460/
Abstract

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.

摘要

几十年来的研究已经确定了与年龄相关的神经退行性疾病以及在较小程度上的神经精神疾病相关的遗传和环境因素。基因组不稳定性,即基因组完整性的丧失,是神经退行性疾病(例如肌萎缩性侧索硬化症、帕金森病、阿尔茨海默病)和精神疾病(例如精神分裂症、自闭症、双相情感障碍)的共同特征。基因组不稳定性与持续的 DNA 损伤的积累以及 DNA 损伤反应 (DDR) 途径的激活有关,还与病理性神经元细胞丢失或衰老有关。通常,DDR 信号确保了基因组和蛋白质组的内稳态在包括神经祖细胞和有丝分裂后神经元在内的分裂细胞中得以维持。然而,这些保护反应的失调部分是由于衰老或环境损伤引起的,导致神经退行性和/或精神疾病的进行性发展。在本期特刊中,我们介绍并强调了神经退行性疾病和神经精神疾病之间的重叠,以及越来越多的临床、基因组和分子证据表明 DNA 损伤和异常 DNA 修复的作用。我们的目标是阐明这个主题的重要性,以揭示针对相关破坏性脑疾病的可能治疗和预防策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2749/11241460/7b81f3735134/ijms-25-07221-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2749/11241460/7b81f3735134/ijms-25-07221-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2749/11241460/7b81f3735134/ijms-25-07221-g001.jpg

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[1]
Introducing the Role of Genotoxicity in Neurodegenerative Diseases and Neuropsychiatric Disorders.

Int J Mol Sci. 2024-6-29

[2]
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[3]
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引用本文的文献

[1]
Green Synthesis and Characterization of Silver Nanoparticles Using Extracts and Evaluation of Their Cytogenotoxic Effects.

Int J Mol Sci. 2025-8-3

[2]
Metal-Induced Genotoxic Events: Possible Distinction Between Sporadic and Familial ALS.

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[3]
Linking Environmental Genotoxins to Neurodegenerative Diseases Through Transcriptional Mutagenesis.

Int J Mol Sci. 2024-10-24

本文引用的文献

[1]
Genomic stress and impaired DNA repair in Alzheimer disease.

DNA Repair (Amst). 2024-7

[2]
What are the DNA lesions underlying formaldehyde toxicity?

DNA Repair (Amst). 2024-6

[3]
Neuronal STING activation in amyotrophic lateral sclerosis and frontotemporal dementia.

Acta Neuropathol. 2024-3-13

[4]
FUS unveiled in mitochondrial DNA repair and targeted ligase-1 expression rescues repair-defects in FUS-linked motor neuron disease.

Nat Commun. 2024-3-9

[5]
Machine learning and XAI approaches highlight the strong connection between and pollutants and Alzheimer's disease.

Sci Rep. 2024-3-5

[6]
Role of the Exposome in Neurodegenerative Disease: Recent Insights and Future Directions.

Ann Neurol. 2024-4

[7]
Meta-analysis of 46,000 germline de novo mutations linked to human inherited disease.

Hum Genomics. 2024-2-23

[8]
The cycad genotoxin methylazoxymethanol, linked to Guam ALS/PDC, induces transcriptional mutagenesis.

Acta Neuropathol Commun. 2024-2-21

[9]
Association of PM Exposure and Alzheimer Disease Pathology in Brain Bank Donors-Effect Modification by Genotype.

Neurology. 2024-3-12

[10]
New Discoveries on Protein Recruitment and Regulation during the Early Stages of the DNA Damage Response Pathways.

Int J Mol Sci. 2024-1-30

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