DNA Double Strand Breaks: A Common Theme in Neurodegenerative Diseases

Author(s): Daniela Merlo, Cristiana Mollinari, Mauro Racaniello, Enrico Garaci, Alessio Cardinale

Journal Name: Current Alzheimer Research

Volume 13 , Issue 11 , 2016

  Journal Home
Translate in Chinese
Become EABM
Become Reviewer
Call for Editor


Accumulation of DNA damage and impairment of DNA repair systems are involved in the pathogenesis of different neurodegenerative diseases. Whenever DNA damage is too extensive, the DNA damage response pathway provides for triggering cellular senescence and/or apoptosis. However, whether the increased level of DNA damage in neurodegenerative disorders is a cause rather than the consequence of neurodegenerative events remains to be established. Among possible DNA lesions, DNA double strand breaks (DSBs) are rare events, nevertheless they are the most lethal form of DNA damage. In neurons, DSBs are particularly deleterious because of their reduced DNA repair capability as compared to proliferating cells.

Here, we provide a description of DSB repair systems and describe human studies showing the presence of several types of DNA lesions in three major neurodegenerative diseases including Alzheimer’s disease (AD), Parkinson’s disease (PD) and Huntington’s disease (HD). Then, we analyze the role of DSB accumulation and deficiency of DSB repair systems in neurodegeneration by examining studies on animal models of neurodegenerative diseases.

Keywords: Alzheimer's disease, DNA damage, DNA repair, DNA double strand breaks, Huntington's disease, neurodegenerative diseases, Parkinson's disease.

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2016
Published on: 01 April, 2016
Page: [1208 - 1218]
Pages: 11
DOI: 10.2174/1567205013666160401114915
Price: $65

Article Metrics

PDF: 62
PRC: 2