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非编码RNA作为精神分裂症病理生理学中的新角色

Non-Coding RNA as Novel Players in the Pathophysiology of Schizophrenia.

作者信息

Gibbons Andrew, Udawela Madhara, Dean Brian

机构信息

The Florey Institute for Neuroscience and Mental Health, 30 Royal Parade, Parkville, VIC 3052, Australia.

The Department of Psychiatry, the University of Melbourne, Parkville, Victoria, Australia.

出版信息

Noncoding RNA. 2018 Apr 12;4(2):11. doi: 10.3390/ncrna4020011.

Abstract

Schizophrenia is associated with diverse changes in the brain's transcriptome and proteome. Underlying these changes is the complex dysregulation of gene expression and protein production that varies both spatially across brain regions and temporally with the progression of the illness. The growing body of literature showing changes in non-coding RNA in individuals with schizophrenia offers new insights into the mechanisms causing this dysregulation. A large number of studies have reported that the expression of microRNA (miRNA) is altered in the brains of individuals with schizophrenia. This evidence is complemented by findings that single nucleotide polymorphisms (SNPs) in miRNA host gene sequences can confer an increased risk of developing the disorder. Additionally, recent evidence suggests the expression of other non-coding RNAs, such as small nucleolar RNA and long non-coding RNA, may also be affected in schizophrenia. Understanding how these changes in non-coding RNAs contribute to the development and progression of schizophrenia offers potential avenues for the better treatment and diagnosis of the disorder. This review will focus on the evidence supporting the involvement of non-coding RNA in schizophrenia and its therapeutic potential.

摘要

精神分裂症与大脑转录组和蛋白质组的多种变化有关。这些变化的基础是基因表达和蛋白质产生的复杂失调,这种失调在大脑区域之间存在空间差异,并随疾病进展而发生时间变化。越来越多的文献表明精神分裂症患者的非编码RNA存在变化,这为导致这种失调的机制提供了新的见解。大量研究报告称,精神分裂症患者大脑中微小RNA(miRNA)的表达发生了改变。微小RNA宿主基因序列中的单核苷酸多态性(SNP)会增加患该疾病的风险,这一发现进一步补充了上述证据。此外,最近的证据表明,其他非编码RNA,如小核仁RNA和长链非编码RNA的表达在精神分裂症中也可能受到影响。了解这些非编码RNA的变化如何导致精神分裂症的发生和发展,为更好地治疗和诊断该疾病提供了潜在途径。本综述将重点关注支持非编码RNA参与精神分裂症的证据及其治疗潜力。

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