Biomarkers of nucleic acid oxidation ? A summary state-of-the-art

0551701 - ÚEM 2022 RIV NL eng J - Článek v odborném periodiku
Chao, M.R. - Evans, M.D. - Hu, Ch.W. - Ji, Y.H.E. - Moller, P. - Rössner ml., Pavel - Cooke, M.S.
Biomarkers of nucleic acid oxidation ? A summary state-of-the-art.
Redox Biology. Roč. 42, jun. (2021), č. článku 101872. ISSN 2213-2317. E-ISSN 2213-2317
Grant CEP: GA MŠMT(CZ) EF16_019/0000798
Institucionální podpora: RVO:68378041
Klíčová slova: Oxidative stress * DNA * RNA * nucleotide pool * biomarkers * DNA repair
Obor OECD: Public and environmental health
Impakt faktor: 10.787, rok: 2021
Způsob publikování: Open access
https://www.sciencedirect.com/science/article/pii/S2213231721000203?via%3Dihub

Oxidatively generated damage to DNA has been implicated in the pathogenesis of a wide variety of diseases. Increasingly, interest is also focusing upon the effects of damage to the other nucleic acids, RNA and the (2?deoxy-)ribonucleotide pools, and evidence is growing that these too may have an important role in disease. LCMS/MS has the ability to provide absolute quantification of specific biomarkers, such as 8-oxo-7,8-dihydro-2?deoxyGuo (8-oxodG), in both nuclear and mitochondrial DNA, and 8-oxoGuo in RNA. However, significant quantities of tissue are needed, limiting its use in human biomonitoring studies. In contrast, the comet assay requires much less material, and as little as 5 ?L of blood may be used, offering a minimally invasive means of assessing oxidative stress in vivo, but this is restricted to nuclear DNA damage only. Urine is an ideal matrix in which to non-invasively study nucleic acid-derived biomarkers of oxidative stress, and considerable progress has been made towards robustly validating these measurements, not least through the efforts of the European Standards Committee on Urinary (DNA) Lesion Analysis. For urine, LC-MS/MS is considered the gold standard approach, and although there have been improvements to the ELISA methodology, this is largely limited to 8oxodG. Emerging DNA adductomics approaches, which either comprehensively assess the totality of adducts in DNA, or map DNA damage across the nuclear and mitochondrial genomes, offer the potential to considerably advance our understanding of the mechanistic role of oxidatively damaged nucleic acids in disease.
Trvalý link: http://hdl.handle.net/11104/0326931