Mutagen influence with different mechanisms of action on DNA global methylation in human whole-blood lymphocytes in vitro

Data that support the evidence of mutagens known to cause epigenetic abnormalities that could potentially result in genomic instability and the development of cancer rather than to modifications in the human genome at the gene and chromosomal levels only. The level of global methylation in human lym...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Russian journal of genetics 2013-07, Vol.49 (7), p.765-770
Hauptverfasser: Smirnikhina, S. A., Voronina, E. S., Strelnikov, V. V., Tanas, A. S., Lavrov, A. V.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Data that support the evidence of mutagens known to cause epigenetic abnormalities that could potentially result in genomic instability and the development of cancer rather than to modifications in the human genome at the gene and chromosomal levels only. The level of global methylation in human lymphocytes in vitro caused by exposure to two mutagens with different mechanisms of action, i.e., dioxidine and methyl methanesulphonate (MMS), was demonstrated in the present study. Global methylation was assessed by methyl-sensitive comet assay. An increase in the level of global methylation to 45.64% was revealed during culturing with dioxidine in a concentration of 0.01 mg/mL ( p < 0.001), while the addition of dioxidine in a concentration of 0.1 mg/mL resulted in a decreased level of methylation up to 42.31% ( p < 0.001). The addition of MMS in concentrations of 0.0025 and 0.01 mg/mL resulted in minor but significant modifications ( p < 0.05) of the global methylation level ranged within natural variations in global methylation. Accordingly, the addition of dioxidine in the concentration of 0.1 mg/mL might cause genomic instability and might be considered a potential carcinogen.
ISSN:1022-7954
1608-3369
DOI:10.1134/S1022795413060124