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Journal of Environmental Pathology, Toxicology and Oncology
Facteur d'impact: 1.625 Facteur d'impact sur 5 ans: 1.63 SJR: 0.402 SNIP: 0.613 CiteScore™: 2.3

ISSN Imprimer: 0731-8898
ISSN En ligne: 2162-6537

Journal of Environmental Pathology, Toxicology and Oncology

DOI: 10.1615/JEnvironPatholToxicolOncol.2014008234
pages 279-293

DNA Repair Kinetic of Hydrogen Peroxide and UVA/B Induced Lesions in Peripheral Blood Leucocytes from Xeroderma Pigmentosum Patients and Healthy Subjects

Elio A. Prieto Gonzalez
Centro de Altos estudios en Ciencias de la Salud, Universidad Abierta Interamericana, Buenos Aires, Argentina
Marta D. Mudry
GIBE; IEGEBA; FCEyN; UBA (Grupo de Investigación en Biologia Evolutiva; Instituto de Ecologia, Genética y Evolución; Facultad de Ciencias Exactas y Naturales-Universidad de Buenos Aires), CONICET, Buenos Aires, Argentina
Ana Maria Palermo
CITEDEF, Buenos Aires, Argentina


The objective of the present work was to study the fine kinetics of DNA repair in xeroderma pigmentosum (XP) syndrome, a complex disorder linked to a deficiency in repair that increases cancer susceptibility. The repair process was evaluated by the comet assay (CA) in cells from 2 XP patients and 9 controls exposed to UVA/B (UVA 366/UVB 280 nm) and H2O2 (150 μM) at temperatures of 4, 15, and 37°C. Samples were taken at 2-min intervals during the first 10 min to analyze the "fine kinetics" repair during the initial phase of the curve, and then at 15, 20, 25, 30, 45, 60, and 120 min. CA evaluation of DNA repair activity points to BER/NER initiation in the first 30 min with both inductors at 37°C and 15°C, but final comet length showed differences according to treatment. Repair kinetics during 120 min showed a good correlation with clinical features in both XP patients. Differences in final comet length were less pronounced in XP cells treated with H2O2 than with UVA/B, probably because the peroxide produces mainly base oxidation but less bulky lesions; UVA/B generates a mixture of both. These findings reinforce the value of CA in testing in DNA repair ability or exposure monitoring.

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