Role of FoxO1 in Acne and Effect of Isotretinoin on FoxO1 Expression

被引:0
|
作者
Kamboj, Parul [1 ]
Khullar, Geeti [1 ]
Handa, Sanjeev [1 ]
Pal, Arnab [2 ]
Saikia, Uma Nahar [3 ]
De, Dipankar [1 ,4 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Dermatol Venereol & Leprol, Chandigarh, India
[2] Postgrad Inst Med Educ & Res, Dept Biochem, Chandigarh, India
[3] Postgrad Inst Med Educ & Res, Dept Histopathol, Chandigarh, India
[4] Postgrad Inst Med Educ & Res, Dept Dermatol Venereol & Leprol, Sect 12, Chandigarh 160012, India
关键词
Acne; androgen receptor; FoxO1; isotretinoin; peroxisome proliferator-activated receptor; GROWTH;
D O I
10.4103/idoj.idoj_455_23
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Nodulocystic acne is a severe type of acne that is known to improve after treatment with isotretinoin. Melnik has hypothesized a unifying concept on the mechanism of acne pathogenesis involving altered expression of Forkhead box O transcription factor (FoxO1) and role of isotretinoin in improving acne via modulating this pathway. Aim: To evaluate the pathway proposed by Melnik in acne pathogenesis by analysing the difference in the expression of FoxO1, peroxisome proliferator-activated receptor (PPAR gamma), and androgen receptor (AR) between acne patients and non-acne controls and the effect of treatment with isotretinoin on change in expression of these genes in acne patients. Results: The gene expression of FoxO1 was non significantly higher in acne patients as compared to controls. After treatment with isotretinoin, a significant decrease in FoxO1 expression in acne patients at mRNA (P = 0.05) level was observed. There was a significant decrease in grade 3 positivity of FoxO1 at protein level (P = 0.0009). A decrease in androgen receptor positivity (P = 0.055) at protein level was also observed. Conclusion: Reduction in FoxO1 expression appears to be an important mechanism of action of isotretinoin in acne.
引用
收藏
页码:252 / 254
页数:3
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