Alimohammadi Mina, Kahkesh Samaneh, Abbasi Amirhosein, Hashemi Mehrdad, Khoshnazar Seyedeh Mahdieh, Taheriazam Afshin, Hushmandi Kiavash
Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Clin Exp Med. 2025 May 6;25(1):140. doi: 10.1007/s10238-025-01660-9.
IgA nephropathy (IgAN), also known as Berger's disease, is a prevalent kidney disorder caused by the accumulation of IgA antibodies in the glomerular tissue. Long noncoding RNAs (lncRNAs), a class of noncoding RNAs longer than 200 nucleotides, play crucial roles in regulating various cellular and molecular processes, including translation, chromatin remodeling, and transcriptional efficiency. Research has highlighted the significant impact of lncRNA imbalances on the development and progression of kidney diseases, including IgAN. These molecules influence several key signaling pathways, such as PI3K/AKT/mTOR, PTEN, Notch, JNK, and immune-related pathways, with their dysregulation contributing to IgAN pathogenesis. This review aims to provide a comprehensive analysis of the molecular signaling pathways involving lncRNAs in IgAN, underscoring their potential as biomarkers for screening, diagnosis, and prevention. Furthermore, it explores the therapeutic potential of lncRNAs as precise targets for personalized treatment strategies.
IgA肾病(IgAN),也称为伯杰氏病,是一种常见的肾脏疾病,由IgA抗体在肾小球组织中积聚引起。长链非编码RNA(lncRNA)是一类长度超过200个核苷酸的非编码RNA,在调节各种细胞和分子过程中发挥着关键作用,包括翻译、染色质重塑和转录效率。研究强调了lncRNA失衡对包括IgAN在内的肾脏疾病的发生和发展具有重大影响。这些分子影响多个关键信号通路,如PI3K/AKT/mTOR、PTEN、Notch、JNK以及免疫相关通路,它们的失调促成了IgAN的发病机制。本综述旨在全面分析IgAN中涉及lncRNA的分子信号通路,强调它们作为筛查、诊断和预防生物标志物的潜力。此外,还探讨了lncRNA作为个性化治疗策略精确靶点的治疗潜力。