4.7 Review

Formation and repair of oxidatively generated damage in cellular DNA

Journal

FREE RADICAL BIOLOGY AND MEDICINE
Volume 107, Issue -, Pages 13-34

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2016.12.049

Keywords

Single base oxidation modifications; DNA oxidative degradation pathways; Measurement of oxidatively generated DNA damage; Repair of oxidized bases

Funding

  1. PFAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo) [2012/12663-1]
  2. PFAPESP (CEPID Redoxoma) [2013/07937-8]
  3. CNPq (Conselho Nacional para o Desenvolvimento Cientifico e Tecnologico) [301307/2013-0]
  4. PRPUSP (Pro-Reitoria de Pesquisa da Universidade de Sao Paulo, NAP Redoxoma) [2011.1.9352.1.8]
  5. National Institute of Environmental Health Sciences of the US National Institutes of Health [ES003598]
  6. Natural Sciences and Engineering Research Council of Canada

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In this review article, emphasis is placed on the critical survey of available data concerning modified nucleobase and 2-deoxyribose products that have been identified in cellular DNA following exposure to a wide variety of oxidizing species and agents including, hydroxyl radical, one-electron oxidants, singlet oxygen, hypochlorous acid and ten-eleven translocation enzymes. In addition, information is provided about the generation of secondary oxidation products of 8-oxo-7,8-dihydroguanine and nucleobase addition products with reactive aldehydes arising from the decomposition of lipid peroxides. It is worth noting that the different classes of oxidatively generated DNA damage that consist of single lesions, intra-and interstrand cross-links were unambiguously assigned and quantitatively detected on the basis of accurate measurements involving in most cases high performance liquid chromatography coupled to electrospray ionization tandem mass spectrometry. The reported data clearly show that the frequency of DNA lesions generated upon severe oxidizing conditions, including exposure to ionizing radiation is low, at best a few modifications per 106 normal bases. Application of accurate analytical measurement methods has also allowed the determination of repair kinetics of several well-defined lesions in cellular DNA that however concerns so far only a restricted number of cases.

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