Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/24938
ชื่อเรื่อง: Patterns and functional roles of LINE-1 and Alu methylation in the keratinocyte from patients with psoriasis vulgaris
ผู้แต่ง: Surasak Yooyongsatit
Kriangsak Ruchusatsawat
Nopadon Noppakun
Nattiya Hirankarn
Apiwat Mutirangura
Jongkonnee Wongpiyabovorn
Keywords: Alterations in LINE-1 methylation are related to many diseases. The levels and patterns of LINE-1 hypomethylation were associated with a higher risk in developing several cancers, having a poorer prognosis and more aggressiveness. To evaluate the LINE-methylated status in psoriasis, LINE-1 methylation in various cells from patients with psoriasis, squamous cell carcinoma and normal controls were assessed by combined bisulfite restriction analysis of LINE-1. The results of the epigenetic changes for intragenic LINE-1 gene expression were also tested on two known expression microarrays. In patients with psoriasis, hypomethylation of LINE-1 and increase in %uCuC were prominent in the keratinocytes when compared with normal controls (P=0.014 and P=0.020, respectively). Alternatively, %uCmC was significantly lower in patients with severe psoriasis compared with mild psoriasis (P=0.022). The receiver-operating characteristic curve analysis indicated the high specificity and sensitivity of uCuC and uCmC in detecting psoriasis and severity of psoriasis. From expression array analysis, genes with LINE-1 were downregulated more than those genes without LINE-1 (P=3.84 × 10−27 and P=2.14 × 10−21, respectively). Modification in LINE-1 methylation may alter the gene expression resulting in a phenotypic change of the psoriatic skin. %uCuC and %uCmC may be used as biomarkers for psoriasis.
วันที่เผยแพร่: 2015
URI: https://www.nature.com/articles/jhg201533
https://ir.swu.ac.th/jspui/handle/123456789/24938
Appears in Collections:Pt-Journal Articles

Files in This Item:
There are no files associated with this item.


Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.