Oxidative Stress and DNA Damage at Telomeres.
Abstract
Oxidative stress is associated with increasing telomere shortening and telomere dysfunction, as well as with numerous pathologies in humans, including inflammatory diseases and cancer. Critically short and dysfunctional telomeres lose their ability to protect chromosome ends, which triggers irreversible growth arrest, termed senescence, or genomic instability. Telomeres are highly sensitive to damage from reactive oxygen species, which increase under conditions of oxidative stress. This work covers the evidence that oxidative damage to telomeric DNA alters telomere maintenance by various mechanisms and describes the DNA repair pathways important for preserving telomere function under oxidative stress conditions.
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Research summary
Oxidative stress contributes to telomere shortening and dysfunction, impacting cellular senescence and genomic stability. The paper is relevant as it addresses mechanisms that could influence the aging process by focusing on telomere maintenance, which is a critical factor in longevity and age-related diseases.
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