Neuroscience and Ophthalmology Group, Institute of Inflammation and Ageing, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
Centre for Trauma Sciences Research, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
Cells. 2021 Sep 14;10(9):2425. doi: 10.3390/cells10092425.
Traumatic brain injury (TBI) represents one of the leading causes of mortality and morbidity worldwide, placing an enormous socioeconomic burden on healthcare services and communities around the world. Survivors of TBI can experience complications ranging from temporary neurological and psychosocial problems to long-term, severe disability and neurodegenerative disease. The current lack of therapeutic agents able to mitigate the effects of secondary brain injury highlights the urgent need for novel target discovery. This study comprises two independent systematic reviews, investigating both microRNA (miRNA) and proteomic expression in rat models of severe TBI (sTBI). The results were combined to perform integrated miRNA-protein co-expression analyses with the aim of uncovering the potential roles of miRNAs in sTBI and to ultimately identify new targets for therapy. Thirty-four studies were included in total. Bioinformatic analysis was performed to identify any miRNA-protein associations. Endocytosis and TNF signalling pathways were highlighted as common pathways involving both miRNAs and proteins found to be differentially expressed in rat brain tissue following sTBI, suggesting efforts to find novel therapeutic targets that should be focused here. Further high-quality investigations are required to ascertain the involvement of these pathways and their miRNAs in the pathogenesis of TBI and other CNS diseases and to therefore uncover those targets with the greatest therapeutic potential.
创伤性脑损伤(TBI)是全球导致死亡和发病的主要原因之一,给全球医疗保健服务和社区带来了巨大的社会经济负担。TBI 的幸存者可能会出现从暂时的神经和心理社会问题到长期、严重残疾和神经退行性疾病等并发症。目前缺乏能够减轻继发性脑损伤影响的治疗药物,这突出表明需要新的靶点发现。这项研究包括两个独立的系统评价,研究了严重 TBI(sTBI)大鼠模型中的 microRNA(miRNA)和蛋白质组表达。将结果结合起来进行 miRNA-蛋白质共表达分析,旨在揭示 miRNA 在 sTBI 中的潜在作用,并最终确定治疗的新靶点。总共纳入了 34 项研究。进行了生物信息学分析以确定任何 miRNA-蛋白质的关联。内吞作用和 TNF 信号通路被突出显示为共同的途径,涉及到 sTBI 后大鼠脑组织中差异表达的 miRNA 和蛋白质,这表明应集中精力寻找新的治疗靶点。需要进一步进行高质量的研究,以确定这些途径及其 miRNA 在 TBI 和其他中枢神经系统疾病发病机制中的参与情况,从而发现具有最大治疗潜力的靶点。