Department of Clinical Biochemistry, Department of Basic Medical Sciences, College of Medicine, Shaqra University, Dawadmi, Saudi Arabia.
Molecular Genetics and Enzymology Department, Human Genetics and Genome Research Institute, National Research Center, Dokki, Cairo, Egypt.
Skin Res Technol. 2024 Mar;30(3):e13639. doi: 10.1111/srt.13639.
MicroRNAs (miRNAs) are small RNA molecules that regulate gene expression in diverse biological processes. They hold promise as therapeutic candidates for targeting human disease pathways, although our understanding of their gene regulatory mechanism remains incomplete. Alopecia areata (AA) is a prevalent inflammatory ailment distinguished by the infiltration of T cells targeting the anagen-stage hair follicles. The scarcity of effective remedies for AA may stem from limited understanding regarding its precise cellular mechanism.
To investigate and examine the importance and role of the miR-200c-3p as a genetic indicator for AA, and its possible impact on disease progression.
Case-control study included 65 patients with AA and 65 matched healthy controls. A real-time PCR technique was used to measure the expression of miR-200c-3p for both groups. Bioinformatic tools were used for prediction with genes and gene-gene interaction, and protein-protein interaction.
The expression levels of miR-200c-3p were significantly higher in AA patients than in healthy controls. We predicted that miR-200c-3p plays a markable role in the development of AA by its effect on the EGFR tyrosine kinase inhibitor resistance pathway.
We were able to identify the influence of miR-200c-3p on both PLCG1 and RPS6KP1 genes which in turn regulate the EGFR tyrosine kinases resistance pathway that displayed the most substantial increase in activity. Our outcomes shed light on the era of the potential theranostic role of this innovative miRNA in AA.
MicroRNAs (miRNAs) 是一种调节多种生物过程中基因表达的小 RNA 分子。它们作为治疗靶点具有很大的潜力,可用于靶向人类疾病途径,尽管我们对其基因调控机制的理解仍不完整。斑秃 (AA) 是一种常见的炎症性疾病,其特征是 T 细胞浸润靶向生长期的毛囊。AA 缺乏有效治疗方法的原因可能是对其确切的细胞机制了解有限。
研究和探讨 miR-200c-3p 作为 AA 的遗传标志物的重要性和作用,及其对疾病进展的可能影响。
纳入 65 例 AA 患者和 65 例匹配的健康对照进行病例对照研究。使用实时 PCR 技术测量两组 miR-200c-3p 的表达。使用生物信息学工具进行预测,包括基因和基因-基因相互作用以及蛋白质-蛋白质相互作用。
AA 患者 miR-200c-3p 的表达水平明显高于健康对照组。我们预测 miR-200c-3p 通过对 EGFR 酪氨酸激酶抑制剂耐药途径的影响,在 AA 的发生发展中发挥重要作用。
我们能够确定 miR-200c-3p 对 PLCG1 和 RPS6KP1 基因的影响,进而调节 EGFR 酪氨酸激酶耐药途径,该途径的活性显著增加。我们的研究结果为这种创新 miRNA 在 AA 中的潜在治疗作用提供了新的认识。