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A Spinal Cord Injury Time and Severity Consensus Transcriptomic Reference Suite in Rat Reveals Translationally-Relevant Biomarker Genes

biorxiv(2024)

Computational Biomedicine Laboratory | Neuronal and Tissue Regeneration Laboratory

Cited 0|Views16
Abstract
Spinal cord injury (SCI) is a devastating condition that leads to motor, sensory, and autonomic dysfunction. Current therapeutic options remain limited, emphasizing the need for a comprehensive understanding of the underlying SCI-associated molecular mechanisms. This study characterized distinct SCI phases and severities at the gene and functional levels, focusing on biomarker gene identification. Our approach involved a systematic review, individual transcriptomic analysis, gene meta-analysis, and functional characterization. We compiled a total of fourteen studies with 273 samples, leading to the identification of severity-specific biomarker genes for injury prognosis (e.g., Srpx2, Hoxb8, Acap1, Snai1, and Aadat) and phase-specific genes for the precise classification of the injury profile (e.g., Il6, Fosl1, Cfp, C1qc, Cp). We investigated the potential transferability of severity-associated biomarkers and identified a twelve-gene signature that predicted injury prognosis from human blood samples. We also report the development of MetaSCI-app - an interactive web application designed for researchers - that allows the exploration and visualization of all generated results (). Overall, we present a transcriptomic reference and provide a comprehensive framework for assessing SCI considering severity and time perspectives. Teaser A transcriptomic meta-analysis of spinal cord injury provides a consensus reference and biomarker genes for injury phase/severity. ### Competing Interest Statement The authors have declared no competing interest.
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要点】:本研究通过系统回顾和转录组分析,建立了一个关于脊髓损伤(SCI)时间和严重程度共识的转录组参考套装,揭示了与SCI相关的翻译上相关的生物标志基因。

方法】:研究采用了系统回顾、个体转录组分析、基因元分析和功能鉴定相结合的方法。

实验】:研究人员汇编了14项研究共273个样本,确定了与损伤预后相关的严重程度特异性生物标志基因(如Srpx2、Hoxb8、Acap1、Snai1和Aadat)和与损伤轮廓精确分类相关的阶段特异性基因(如Il6、Fosl1、Cfp、C1qc和Cp)。研究人员还调查了严重程度相关生物标志物的潜在可转移性,并确定了一个可以从人类血液样本预测损伤预后的12基因签名。此外,研究人员还报告了MetaSCI-app的开发,这是一个用于研究人员交互式网络应用程序,允许探索和可视化所有生成结果。