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Identification of key transcription factors associated with cerebral ischemia-reperfusion injury based on gene-set enrichment analysis | |
2019-06 | |
发表期刊 | INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE |
ISSN | 1107-3756 |
卷号 | 43期号:6页码:2429-2439 |
发表状态 | 已发表 |
DOI | 10.3892/ijmm.2019.4159 |
摘要 | Cerebral ischemia-reperfusion injury (CIRI) usually causes detrimental complications following reperfusion therapy in stroke patients. The present study systematically investigated the regulatory mechanism involved in the pathogenesis of CIRI using gene set enrichment analysis of the transient middle cerebral artery occlusion mouse stroke model. The results revealed a total of 13 CIRI-related transcription factors (TFs), including CCAAT enhancer binding protein b (Cebpb), Cebpa, early growth response-1, Fos, Rela, Jund, signal transduction and activator of transcription 5a/b, transformation related protein 53, GLI family zinc finger 2 (Gli2), Sp3, TF AP-2 (Tfap2a) and spleen focus forming virus proviral integration oncogene (Spi1). To the best of our knowledge, five TFs (Cebpa, Gli2, Sp3, Tfap2a and Spi1) were the first to be reported associated with CIRI in the present study. The five novel CIRI-related TFs were mainly associated with pathways of inflammation and responses to reperfusion, including the tumor necrosis factor signaling pathway (Gli2, Spi1 and Tfap2a, P=0.0035, 0.0035 and 0.048, respectively), interleuking-17 signaling pathway (Cebpa, Gli2, Sp3, Spi1 and Tfap2a, P=0.019, 0.047, 0.019, 0.035 and 0.005, respectively) and fluid shear stress and atherosclerosis (Gli2, Sp3, Spi1 and Tfap2a, P=0.047, 0.046, 0.013 and 0.003, respectively). These results may improve understanding of the potential molecular mechanism underlying the pathogenesis of CIRI at the genome-wide level. |
关键词 | ischemic stroke cerebral ischemia-reperfusion injury transcription factor gene-set enrichment analysis functional pathway enrichment |
收录类别 | SCI ; SCIE |
语种 | 英语 |
资助项目 | National Natural Science Foundation of China[81471767] ; National Natural Science Foundation of China[81871464] |
WOS研究方向 | Research & Experimental Medicine |
WOS类目 | Medicine, Research & Experimental |
WOS记录号 | WOS:000467649900015 |
出版者 | SPANDIDOS PUBL LTD |
WOS关键词 | NF-KAPPA-B ; SIGNALING PATHWAY ; ARTERY OCCLUSION ; BRAIN ISCHEMIA ; C/EBP-ALPHA ; EXPRESSION ; ACTIVATION ; DAMAGE ; CONTRIBUTES ; PROTECTS |
原始文献类型 | Article |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/40839 |
专题 | 免疫化学研究所_公共科研平台_生物医学大数据平台 |
通讯作者 | Lv, Jin; Jiang, Wei-Jian |
作者单位 | 1.PLA Rocket Force Characterist Med Ctr, New Era Stroke Care & Res Inst, Dept Vasc Neurosurg, 16 Xin Wai Ave, Beijing 100088, Peoples R China 2.ShanghaiTech Univ, Shanghai Inst Adv Immunochem Studies, Shanghai 201210, Peoples R China 3.PLA Rocket Force Characterist Med Ctr, Dept Nucl & Radiat Injury, Beijing 100088, Peoples R China |
推荐引用方式 GB/T 7714 | Zhang, Ying-Ying,Wang, Kai,Liu, Yun-E,et al. Identification of key transcription factors associated with cerebral ischemia-reperfusion injury based on gene-set enrichment analysis[J]. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE,2019,43(6):2429-2439. |
APA | Zhang, Ying-Ying.,Wang, Kai.,Liu, Yun-E.,Wang, Wei.,Liu, Ao-Fei.,...&Jiang, Wei-Jian.(2019).Identification of key transcription factors associated with cerebral ischemia-reperfusion injury based on gene-set enrichment analysis.INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE,43(6),2429-2439. |
MLA | Zhang, Ying-Ying,et al."Identification of key transcription factors associated with cerebral ischemia-reperfusion injury based on gene-set enrichment analysis".INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 43.6(2019):2429-2439. |
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