Abstract
Objective. To analyze the methylation status of miR-124a loci in synovial tissues of rheumatoid arthritis (RA) patients using methylation-specific polymerase chain reaction (MSP). Materials and Methods. DNA obtained from the frozen tissue of 7 RA samples, 6 osteoarthritis (OA) samples, and 3 healthy controls were undergoing bisulfite conversion and then analyzed for miR-124a promoter methylation using MSP assay. Results. miR-124-a1 and miR-124-a2 promoter methylation were both seen in 71.4% of RA samples compared to 16.7% of OA samples. miR-124-a3 promoter methylation was seen in 57.1% of RA samples and 0% of OA samples. All the three loci were unmethylated in 3 healthy controls. Conclusion. The methylation status of miR-124a seen in this study concurs with that reported in tumor cells, indicating epigenetic dysregulation constituents, a mechanism in the development of rheumatoid arthritis. © 2013 Qiao Zhou et al.
Cite
CITATION STYLE
Zhou, Q., Long, L., Shi, G., Zhang, J., Wu, T., & Zhou, B. (2013). Research of the methylation status of mir-124a gene promoter among rheumatoid arthritis patients. Clinical and Developmental Immunology, 2013. https://doi.org/10.1155/2013/524204
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.