Department of Neurobiology, Chongqing Key Laboratory of Neurobiology, Third Military Medical University, Chongqing 400038, China.
Cadet Brigade, Third Military Medical University, Chongqing 400038, China.
Biomed Res Int. 2017;2017:6423021. doi: 10.1155/2017/6423021. Epub 2017 Oct 15.
It is well known spinal cord injury (SCI) can cause chronic neuropathic pain (NP); however its underlying molecular mechanisms remain elusive. This study aimed to disclose differentially expressed genes (DEGs) and activated signaling pathways in association with SCI induced chronic NP, in order to identify its diagnostic and therapeutic targets. Microarray dataset GSE5296 has been downloaded from Gene Expression Omnibus (GEO) database. Significant analysis of microarray (SAM), Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, and pathway network analysis have been used to compare changes of DEGs and signaling pathways between the SCI and sham-injury group. As a result, DEGs analysis showed there were 592 DEGs with significantly altered expression; among them Ccl3 expression showed the highest upregulation which implicated its association with SCI induced chronic NP. Moreover, KEGG analysis found 209 pathways changed significantly; among them the most significantly activated one is MAPK signaling pathway, which is in line with KEGG analysis results. Our results show Ccl3 is highly associated with SCI induced chronic NP; as the exosomes with Ccl3 can be easily and efficiently detected in peripheral blood, Ccl3 may serve as a potential prognostic target for the diagnosis and treatment of SCI induced chronic NP.
众所周知,脊髓损伤(SCI)可导致慢性神经性疼痛(NP);然而,其潜在的分子机制仍难以捉摸。本研究旨在揭示与 SCI 诱导的慢性 NP 相关的差异表达基因(DEGs)和激活的信号通路,以确定其诊断和治疗靶点。从基因表达综合数据库(GEO)下载了微阵列数据集 GSE5296。采用显著分析微阵列(SAM)、京都基因与基因组百科全书(KEGG)通路富集分析和通路网络分析,比较 SCI 组和假手术组 DEGs 和信号通路的变化。结果显示,DEGs 分析显示有 592 个 DEGs 表达明显改变;其中 Ccl3 的表达上调最为显著,表明其与 SCI 诱导的慢性 NP 有关。此外,KEGG 分析发现 209 条通路发生显著改变;其中最显著激活的是 MAPK 信号通路,与 KEGG 分析结果一致。我们的研究结果表明 Ccl3 与 SCI 诱导的慢性 NP 高度相关;由于 Ccl3 的外泌体可在外周血中被轻松有效地检测到,Ccl3 可能成为 SCI 诱导的慢性 NP 诊断和治疗的潜在预后靶点。