Rani Anchal, Kaur Gagandeep, Kumar Ravinder, Sachan Rohan Samir Kumar, Kumar Mukesh, Sable Harsh, Al Tawaha Abdel Rahman Mohammad, Malik Shahid, Karnwal Arun, Malik Tabarak
School of Allied and Health Care Sciences, GNA University, Phagwara, India.
School of Pharmacy, GNA University, Phagwara, India.
Biomed Res Int. 2025 Mar 27;2025:7002918. doi: 10.1155/bmri/7002918. eCollection 2025.
DNA methylation is an epigenetic mechanism modulating gene expression without altering the genetic sequence and plays a significant role in skin disorders. Methylation patterns on specific genes can lead to either overexpression or suppression, impacting cellular functions critical to skin health. Skin disorders such as atopic dermatitis, eczema, androgenetic alopecia, systemic lupus erythematosus, psoriasis, and systemic sclerosis have been linked to abnormal DNA methylation, which contributes to disease progression through immune dysregulation, barrier dysfunction, and inflammation. The methylation of genes like S100A2 and FCERIG in atopic dermatitis or FLG in eczema illustrates how modifications affect immune pathways and skin integrity. Recent advancements in DNA methylation analysis have enhanced the precision of detecting methylation levels and their influence on gene expression, leading to a deeper understanding of disease mechanisms. Identifying aberrant methylation patterns offers potential biomarkers for early diagnosis and therapeutic targets, especially in autoimmune and inflammatory skin diseases. Further exploration of epigenetic changes could pave the way for innovative treatments, addressing underlying epigenetic disruptions that characterize these conditions.
DNA甲基化是一种表观遗传机制,可在不改变基因序列的情况下调节基因表达,在皮肤疾病中起重要作用。特定基因上的甲基化模式可导致基因过表达或抑制,影响对皮肤健康至关重要的细胞功能。特应性皮炎、湿疹、雄激素性脱发、系统性红斑狼疮、银屑病和系统性硬化症等皮肤疾病与异常的DNA甲基化有关,DNA甲基化通过免疫失调、屏障功能障碍和炎症促进疾病进展。特应性皮炎中S100A2和FCERIG等基因的甲基化,或湿疹中FLG基因的甲基化,说明了这些修饰如何影响免疫途径和皮肤完整性。DNA甲基化分析的最新进展提高了检测甲基化水平及其对基因表达影响的精确度,从而加深了对疾病机制的理解。识别异常的甲基化模式可为早期诊断提供潜在的生物标志物和治疗靶点,尤其是在自身免疫性和炎症性皮肤病中。进一步探索表观遗传变化可为创新治疗铺平道路,解决这些疾病所特有的潜在表观遗传紊乱问题。