Xiang-Ya Hospital Central South University, 87 XiangYa Road, Changsha 410008, Hunan, China.
The Second Clinical Hospital, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Comb Chem High Throughput Screen. 2021;24(7):976-985. doi: 10.2174/1386207323999201124204755.
Recent studies have shown that patients with psoriasis, a chronic inflammatory skin disorder that may accompany the serious systemic disease, are at risk of developing sudden sensorineural hearing loss. The pathogenesis remains unclear, and the mechanisms of this disorder are difficult to explore in the clinical setting due to psoriasis hearing loss's infrequent incidence. Here, we aimed to identify key candidate genes that may be involved in the pathogenesis of psoriatic hearing loss.
In the present study, through online databases and literature review, we utilized microRNA-mRNA network analysis and gene ontology annotation analysis, coupled with experimental data from clinical samples, to investigate the relationship between psoriasis and hearing loss.
We identified nine miRNAs implicated in both psoriasis and the auditory system. By using bioinformatics techniques, 12 target genes were identified. Finally, the gap junction beta-2 protein (GJB2) was found to be relevant to both psoriasis and hearing loss. Also, the expression of connexin 26 (Cx26), encoded by GJB2, was significantly downregulated in psoriatic patients' plasma (p < 0.0001) and was negatively correlated with psoriasis area and severity index (PASI) clinical score (r, -0.286; p = 0.036).
GJB2 is a potential candidate gene for hearing loss in psoriasis.
最近的研究表明,患有银屑病的患者(一种可能伴随严重系统性疾病的慢性炎症性皮肤疾病)有发生突发性感觉神经性听力损失的风险。其发病机制尚不清楚,由于银屑病性听力损失的罕见发病率,该疾病的发病机制在临床环境中难以探索。在这里,我们旨在确定可能参与银屑病性听力损失发病机制的关键候选基因。
在本研究中,我们通过在线数据库和文献综述,利用 microRNA-mRNA 网络分析和基因本体注释分析,结合临床样本的实验数据,研究了银屑病与听力损失之间的关系。
我们鉴定出了 9 种与银屑病和听觉系统都相关的 miRNA。通过生物信息学技术,我们确定了 12 个靶基因。最后,发现缝隙连接β-2 蛋白(GJB2)与银屑病和听力损失都相关。此外,GJB2 编码的连接蛋白 26(Cx26)在银屑病患者的血浆中的表达显著下调(p<0.0001),并且与银屑病面积和严重程度指数(PASI)临床评分呈负相关(r,-0.286;p=0.036)。
GJB2 是银屑病听力损失的潜在候选基因。