Counteraction of Oxidative Stress by Vitamin E Affects Epigenetic Regulation by Increasing Global Methylation and Gene Expression of MLH1 and DNMT1 Dose Dependently in Caco-2 Cells

Autor(en)
Katja Zappe, Angelika Pointner, Olivier J. Switzeny, Ulrich Magnet, Elena Tomeva, Jutta Heller, George Mare, Karl Heinz Wagner, Siegfried Knasmueller, Alexander G. Haslberger
Abstrakt

Obesity- or diabetes-induced oxidative stress is discussed as a major risk factor for DNA damage. Vitamin E and many polyphenols exhibit antioxidative activities with consequences on epigenetic regulation of inflammation and DNA repair. The present study investigated the counteraction of oxidative stress by vitamin E in the colorectal cancer cell line Caco-2 under normal (1 g/l) and high (4.5 g/l) glucose cell culture condition. Malondialdehyde (MDA) as a surrogate marker of lipid peroxidation and reactive oxygen species (ROS) was analyzed. Gene expression and promoter methylation of the DNA repair gene MutL homolog 1 (MLH1) and the DNA methyltransferase 1 (DNMT1) as well as global methylation by LINE-1 were investigated. Results revealed a dose-dependent counteracting effect of vitamin E on H2O2-induced oxidative stress. Thereby, 10 μM vitamin E proved to be more efficient than did 50 μM in reducing MDA. Further, an induction of MLH1 and DNMT1 gene expression was noticed, accompanied by an increase in global methylation. Whether LINE-1 hypomethylation is a cause or effect of oxidative stress is still unclear. In conclusion, supplementation of exogenous antioxidants like vitamin E in vitro exhibits beneficial effects concerning oxidative stress as well as epigenetic regulation involved in DNA repair.

Organisation(en)
Department für Ernährungswissenschaften
Externe Organisation(en)
Johannes Gutenberg-Universität Mainz, Universität Wien, Medizinische Universität Wien
Journal
Oxidative Medicine and Cellular Longevity
Band
2018
Anzahl der Seiten
13
ISSN
1942-0900
DOI
https://doi.org/10.1155/2018/3734250
Publikationsdatum
03-2018
Peer-reviewed
Ja
ÖFOS 2012
106002 Biochemie
Schlagwörter
ASJC Scopus Sachgebiete
Ageing, Biochemistry, Cell Biology
Sustainable Development Goals
SDG 3 – Gesundheit und Wohlergehen
Link zum Portal
https://ucrisportal.univie.ac.at/de/publications/583e2f98-8143-402c-847a-2844f17656b1