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Genes associated with disc degeneration identified using microarray gene expression profiling and bioinformatics analysis

机译:使用微阵列基因表达谱和生物信息学分析鉴定与椎间盘退变相关的基因

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Disc degeneration is strongly associated with back or neck pain, sciatica, and disc herniation or prolapse. It places an enormous economic burden on society and can greatly affect quality of life. Alternative treatment approaches, such as genetic therapies, are urgently needed to slow or reverse the disc degeneration process. We downloaded gene expression data from Gene Expression Omnibus during various stages of disc degeneration and identified differentially expressed genes (DEGs) as well as dysfunctional pathways through comparisons with controls. We identified 2 significant DEGs between grade II and III discs and 8 significant DEGs between grade II and IV discs. By constructing an interactive network of the DEGs, we found that mitogen-activated protein family genes and Ras homologous (Rho) family genes - in particular, MAP2K6 and RHOBTB2 - may play important roles in the progression of degeneration of grade III and IV discs, respectively. MAP2K6 and RHOBTB2 may be specific therapeutic molecular targets in the treatment of disc degeneration. However, further experiments are needed to confirm this result.
机译:椎间盘退变与背部或颈部疼痛,坐骨神经痛和椎间盘突出或脱垂密切相关。它给社会带来了巨大的经济负担,并可能极大地影响生活质量。迫切需要替代疗法,例如基因疗法,以减慢或逆转椎间盘退变过程。我们在椎间盘退变的各个阶段从Gene Expression Omnibus下载了基因表达数据,并通过与对照进行比较来鉴定差异表达的基因(DEG)以及功能障碍的途径。我们确定了II级和III级光盘之间的2个重要DEG和II级和IV级光盘之间的8个重要DEG。通过构建DEG的互动网络,我们发现有丝分裂原激活的蛋白家族基因和Ras同源(Rho)家族基因-特别是MAP2K6和RHOBTB2-在III级和IV级椎间盘退变的进展中可能起重要作用,分别。 MAP2K6和RHOBTB2可能是治疗椎间盘退变的特定治疗分子靶标。但是,需要进一步的实验来确认该结果。

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