DNA Methylation
Conditions
Brief summary
A buccal swab will be taken using a cotton stick by rubbing it against the buccal mucosa. Samples will be taken from the same participant at different timepoints. DNA will be extracted from the buccal cells on the swabs using a commercial extraction kit and will be quantified by a nano-drop spectrophotometer. We will determine global and gene-specific methylation and hydroxymethylation alterations by UPLC/MS/MS. Hydrolyzed DNA into individual nucleosides will be analyzed for the quantitative measurement of 5-methylCytosine and 5-hydroxymethylCytosine on Triple Quadrupole UPLC/MS/MS platform. Secondly, specific methylation in the CpG islands of tumor suppressor and promoter genes, and genes involved in the oxidative stress pathways will be assessed by PCR-pyrosequencing.
Interventions
Buccal swabs will be taken from the volunteers
Sponsors
Study design
Eligibility
Inclusion criteria
* Caucasian
Exclusion criteria
\-
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| %Methylation (%) | 5 weeks |
Secondary
| Measure | Time frame |
|---|---|
| %Hydroxymethylation (%) | 5 weeks |
Countries
Belgium