DNA damage by singlet oxygen and cellular protective mechanisms
Abstract
Reactive oxygen species, as singlet oxygen ((1)O(2)) and hydrogen peroxide, are continuously generated by aerobic organisms, and react actively with biomolecules. At excessive amounts, (1)O(2) induces oxidative stress and shows carcinogenic and toxic effects due to oxidation of lipids, proteins and nucleic acids. Singlet oxygen is able to react with DNA molecule and may induce G to T transversions due to 8-oxodG generation. The nucleotide excision repair, base excision repair and mismatch repair have been implicated in the correction of DNA lesions induced by (1)O(2) both in prokaryotic and in eukaryotic cells. (1)O(2) is also able to induce the expression of genes involved with the cellular responses to oxidative stress, such as NF-κB, c-fos and c-jun, and genes involved with tissue damage and inflammation, as ICAM-1, interleukins 1 and 6. The studies outlined in this review reinforce the idea that (1)O(2) is one of the more dangerous reactive oxygen species to the cells, and deserves our attention.
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Singlet oxygen reacts with all four deoxynucleotide bases, preferring guanine, and produces 8-oxo-G as its main product.
“Singlet oxygen reacts with all four deoxynucleotide bases with guanine as its preference, generating 8-oxo-7,8-dihydroguanine (8-oxo-G) as the major product [5].”
From Functional interplay between ATM/ATR-mediated DNA damage response and DNA repair pathways in oxidative stress (2014) · cites this paper as [5]
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References 205 · Cited by 205
- Authors
- Agnez-Lima, L. F., Melo, J. T. A., Silva, A. E., Oliveira, A. H. S., Timoteo, A. R. S., Lima-Bessa, K. M., Martinez, G. R., Medeiros, M. H. G., Di Mascio, P., Galhardo, R. S., & Menck, C. F. M.
- Affiliations
- Universidade Federal do Rio Grande do Norte (BR)
- Universidade de São Paulo (BR)
- Venue
- Mutation Research/Reviews in Mutation Research
- Publisher
- Elsevier BV
- Published
- 2012-07
- Volume
- 751
- Issue
- 1
- Pages
- 15-28
- ISSN
- 1383-5742 (ISSN-L)
- OpenAlex
- W2011985542
- Cited by
- 205
- References
- 205
- Citations by year
- 2026: 9 · 2025: 13 · 2024: 12 · 2023: 16 · 2022: 24 · 2021: 18 · 2020: 22 · 2019: 16 · 2018: 7 · 2017: 13 · 2016: 12 · 2015: 13 · 2014: 19 · 2013: 9 · 2012: 2
- FWCI
- 5.52
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Mutation Research/Reviews in Mutation Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- CAPES
- INCT-Redox Processes in Biomedicine, Redoxoma-CNPq
- FAPESP
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Carcinogens and Genotoxicity Assessment
- Keywords
- singlet oxygen, DNA damage, reactive oxygen species, oxidative stress, 8-oxoguanine, G to T transversions, nucleotide excision repair, base excision repair, DNA mismatch repair, NF-κB, c-fos, c-Jun, ICAM-1, interleukin-1, interleukin-6, inflammation, carcinogenesis
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