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DNA damage and repair: Relevance to mechanisms of neurodegeneration

Journal

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1097/NEN.0b013e31816ff780

Keywords

Alzheimer disease; amyotrophic lateral sclerosis; apoptosis; aprataxin; cortical neuron; motor neuron; p53

Funding

  1. NIA NIH HHS [AG016282, R01 AG016282, R01 AG016282-08] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS034100-10, R01 NS052098-04, NS034100, NS052098, R01 NS052098, R01 NS034100] Funding Source: Medline

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DNA damage is a form of cell stress and injury that has been implicated in the pathogenesis of many neurologic disorders, including amyotrophic lateral sclerosis, Alzheimer disease, Down syndrome, Parkinson disease, cerebral ischemia, and head trauma. However, most data reveal only associations, and the role for DNA damage in direct mechanisms of neurodegeneration is vague with respect to being a definitive upstream cause of neuron cell death, rather than a consequence of the degeneration. Although neurons seem inclined to develop DNA damage during oxidative stress, most of the existing work on DNA damage and repair mechanisms has been done in the context of cancer biology using cycling non-neuronal cells but not nondividing (i.e. postmitotic) neurons. Nevertheless, the identification of mutations in genes that encode proteins that function in DNA repair and DNA damage response in human hereditary DNA repair deficiency syndromes and ataxic disorders is establishing a mechanistic precedent that clearly links DNA damage and DNA repair abnormalities with progressive neurodegeneration. This review summarizes DNA damage and repair mechanisms and their potential relevance to the evolution of degeneration in postinitotic neurons.

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