Chronic oxidative damage together with genome repair deficiency in the neurons is a double whammy for neurodegeneration: Is damage response signaling a potential therapeutic target?

Haibo Wang, Prakash Dharmalingam, Velmarini Vasquez, Joy Mitra, Istvan Boldogh, K. S. Rao, Thomas A. Kent, Sankar Mitra, Muralidhar L. Hegde

    Research output: Contribution to journalReview article

    10 Scopus citations

    Abstract

    A foremost challenge for the neurons, which are among the most oxygenated cells, is the genome damage caused by chronic exposure to endogenous reactive oxygen species (ROS), formed as cellular respiratory byproducts. Strong metabolic activity associated with high transcriptional levels in these long lived post-mitotic cells render them vulnerable to oxidative genome damage, including DNA strand breaks and mutagenic base lesions. There is growing evidence for the accumulation of unrepaired DNA lesions in the central nervous system (CNS) during accelerated aging and progressive neurodegeneration. Several germ line mutations in DNA repair or DNA damage response (DDR) signaling genes are uniquely manifested in the phenotype of neuronal dysfunction and are etiologically linked to many neurodegenerative disorders. Studies in our lab and elsewhere revealed that pro-oxidant metals, ROS and misfolded amyloidogenic proteins not only contribute to genome damage in CNS, but also impede their repair/DDR signaling leading to persistent damage accumulation, a common feature in sporadic neurodegeneration. Here, we have reviewed recent advances in our understanding of the etiological implications of DNA damage vs. repair imbalance, abnormal DDR signaling in triggering neurodegeneration and potential of DDR as a target for the amelioration of neurodegenerative diseases.

    Original languageEnglish (US)
    Pages (from-to)163-176
    Number of pages14
    JournalMechanisms of Ageing and Development
    Volume161
    DOIs
    StatePublished - Jan 1 2017

    Keywords

    • DNA damage
    • DNA damage response
    • DNA repair defects
    • Neurodegeneration

    ASJC Scopus subject areas

    • Aging
    • Developmental Biology

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