The methylation pattern of p16INK4a gene promoter in psoriatic epidermis and its clinical significance
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Chen, M.
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机构:Chinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R China
Chen, M.
Chen, Z-Q.
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Chinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R ChinaChinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R China
Chen, Z-Q.
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Cui, P-G.
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机构:Chinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R China
Cui, P-G.
Yao, X.
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机构:Chinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R China
Yao, X.
Li, Y-M.
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机构:Chinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R China
Li, Y-M.
Li, A-S.
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机构:Chinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R China
Li, A-S.
Gong, J-Q.
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机构:Chinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R China
Gong, J-Q.
Cao, Y-H.
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机构:Chinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R China
Cao, Y-H.
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[1] Chinese Acad Med Sci, Inst Dermatol, Dept Clin Dermatol & Immunol, Nanjing, Peoples R China
Background Alteration of the p16(INK4a) gene by epigenetic changes has been described in some hyperproliferative skin diseases, but its importance in psoriasis has not yet been established. Objectives To investigate the methylation status of the p16(INK4a) gene in psoriatic epidermis, its clinical significance and the possible epigenetic mechanisms of psoriasis. Methods DNA and RNA specimens were obtained from the lesional epidermis of 56 patients with plaque psoriasis. Methylation-specific polymerase chain reaction (PCR) and DNA sequencing were used to detect the density and sites of methylation in the p16(INK4a) promoter region. The reverse transcription-PCR technique was applied to detect the mRNA expression of p16(INK4a). Results p16(INK4a) gene promoter methylation was shown in 17 of 56 (30%) patients with psoriasis. Psoriasis Area and Severity Index scores in patients showing methylation were higher than in those who did not (P < 0.05). The mRNA expression level of p16(INK4a) in the methylated group was significantly lower than in the unmethylated group (t = 2.515, P = 0.015). In the methylated group, about 50% of the CpG islands were methylated in the promoter region. Conclusions Overall, methylation of the p16(INK4a) gene promoter is found in psoriatic epidermis, which is associated with the mRNA level of p16(INK4a) expression and activity of the disease. These data indicate that methylation of the p16(INK4a) promoter may play a potential role in the pathogenesis of psoriasis.