Related Experiment Video
Updated: May 25, 2025

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images
Published on: September 7, 2017
Global DNA Methylation and DNA Methyltransferase Status Among Cigarette Smokers in Saudi
Areej AlAmeer1, Samar Sultan1,2
1Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 80200, Saudi Arabia.
Abstract:
Smoking is a serious public health concern worldwide. It is a common environmental factor causing epigenetic alterations. This study aimed to explore the effect of smoking on DNA methylation by quantifying global DNA methylation, measuring the concentrations of plasma DNA methyltransferases (DNMT1, DNMT3A, and DNMT3B) among cigarette smokers in Saudi, and comparing these results with those of nonsmokers. Whole blood specimens were collected from Saudi cigarette smokers (n = 36) and non-smokers as controls (n = 36). Global DNA alteration was determined by a 5-methylation Cytosine (5-mC) colorimetric assay, and the concentration of DNMT proteins was measured by enzyme-linked immunosorbent assay (ELISA). DNA hypomethylation was found in smokers compared with controls (p < 0.001). Cigarette smokers showed significantly increased DNMT concentrations (DNM-1, DNMT-3A, and DNMT-3B) (p < 0.005). Global DNA hypomethylation correlated significantly with smoking duration (r = -0.854, p = 0.040) but not with other clinical parameters. In addition, DNMTs also were significantly correlated with smoking duration DNMT1 (r = 0.033, p = 0.002), DNMT3A (r = 0.431, p < 0.001), and DNMT3B (r = 0.553, p = 0.015). Our findings suggest that cigarette smoke induces epigenetic dysregulation, a principal player in cancer and various diseases through global DNA hypomethylation and high concentrations of DNMTs among cigarette smokers compared with nonsmokers.
Related Concept Videos
Epigenetic Regulation
Phase II Reactions: Methylation Reactions
The mechanism of methylation unfolds in two stages. The first stage sees a methyltransferase enzyme facilitating the transfer of a methyl group from S-adenosylmethionine (SAM) to the substrate, forming S-adenosylhomocysteine (SAH). The second stage involves further metabolism of SAH into homocysteine, which can be recycled...

