Li Xiaoqing, Yang Li, Zhu Longfei, Sun Jingying, Xu Cuixiang, Sun Lijun
Shaanxi Provincial Key Laboratory of Infection and Immune Diseases, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi, China.
Department of Dermatology, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi, China.
Front Mol Biosci. 2025 Feb 26;12:1536477. doi: 10.3389/fmolb.2025.1536477. eCollection 2025.
Numerous studies have reported that dysregulation of fatty acid metabolic pathways is associated with the pathogenesis of vitiligo, in which arachidonic acid metabolism (AAM) plays an important role. However, the molecular mechanisms of AAM in the pathogenesis of vitiligo have not been clarified. Therefore, we aimed to identify the biomarkers and molecular mechanisms associated with AAM in vitiligo using bioinformatics methods.
The GSE75819 and GSE65127 datasets were used in this study as the training and validation sets, respectively, along with 58 AAM-related genes (AAM-RGs). The differentially expressed genes (DEGs) between the lesional and control groups in the training set were identified through differential expression analysis. A biomarker-based nomogram was constructed to predict the risk of vitiligo.
15 overlapping candidate genes were obtained between the DEGs and AAM-RGs. Machine-learning algorithms were used to identify six key genes as , , , , , and . In both the training and validation sets, , , and . In both the training and validation sets, , , and were regarded as biomarkers. A nomogram based on these biomarkers showed potential for predicting the risk of vitiligo. Functional enrichment, immune cell infiltration, and regulatory network analyses were used to elucidate the molecular mechanisms.
In conclusion, , , and were implicated in AAM to influence the pathogenesis of vitiligo. These findings offer insights into vitiligo treatment, although further research is needed for a comprehensive understanding.
大量研究报道脂肪酸代谢途径失调与白癜风的发病机制有关,其中花生四烯酸代谢(AAM)起重要作用。然而,AAM在白癜风发病机制中的分子机制尚未阐明。因此,我们旨在利用生物信息学方法确定与白癜风中AAM相关的生物标志物和分子机制。
本研究分别使用GSE75819和GSE65127数据集作为训练集和验证集,以及58个与AAM相关的基因(AAM-RGs)。通过差异表达分析确定训练集中病变组和对照组之间的差异表达基因(DEGs)。构建基于生物标志物的列线图以预测白癜风的风险。
在DEGs和AAM-RGs之间获得了15个重叠的候选基因。使用机器学习算法确定了6个关键基因,分别为 、 、 、 、 和 。在训练集和验证集中, 、 和 。在训练集和验证集中, 、 和 被视为生物标志物。基于这些生物标志物的列线图显示出预测白癜风风险的潜力。使用功能富集、免疫细胞浸润和调控网络分析来阐明分子机制。
总之, 、 和 参与AAM以影响白癜风的发病机制。这些发现为白癜风治疗提供了见解,尽管需要进一步研究以全面理解。