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Identification of Blood Circular RNAs as Potential Biomarkers for Acute Ischemic Stroke.
Lu, Dan; Ho, Eric S; Mai, Hongcheng; Zang, Jiankun; Liu, Yanfang; Li, Yufeng; Yang, Bing; Ding, Yan; Tsang, Chi Kwan; Xu, Anding.
Afiliação
  • Lu D; Department of Neurology and Stroke Center, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Ho ES; Clinical Neuroscience Institute, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Mai H; Department of Biology, Lafayette College, Easton, PA, United States.
  • Zang J; Department of Computer Science, Lafayette College, Easton, PA, United States.
  • Liu Y; Department of Neurology and Stroke Center, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Li Y; Clinical Neuroscience Institute, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Yang B; Department of Neurology and Stroke Center, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Ding Y; Clinical Neuroscience Institute, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Tsang CK; Department of Neurology and Stroke Center, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Xu A; Clinical Neuroscience Institute, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Front Neurosci ; 14: 81, 2020.
Article em En | MEDLINE | ID: mdl-32116524
ABSTRACT
Many hospitals lack facilities for accurate diagnosis of acute ischemic stroke (AIS). Circular RNA (circRNA) is highly expressed in the brain and is closely associated with stroke. In this study, we examined whether the blood-borne circRNAs could be promising candidates as adjunctive diagnostic biomarkers and their pathophysiological roles after stroke. We profiled the blood circRNA expression in mice subjected to experimental focal cerebral ischemia and validated the selected circRNAs in AIS patients. We demonstrated that 128, 198, and 789 circRNAs were significantly altered at 5 min, 3 h, and 24 h after ischemic stroke, respectively. Our bioinformatics analysis revealed that the circRNA-targeted genes were associated with the Hippo signaling pathway, extracellular matrix-receptor interaction, and fatty acid metabolism at 5 min, 3 h and 24 h after ischemic stroke, respectively. We verified that many of these circRNAs existed in the mouse brain. Furthermore, we found that most of the predicted circRNA-miRNA interactions apparently exhibited functional roles in terms of regulation of their target gene expression in the brain. We also verified that many of these mouse circRNAs were conserved in human. Finally, we found that circBBS2 and circPHKA2 were differentially expressed in the blood of AIS patients. These results demonstrate that blood circRNAs may serve as potential biomarkers for AIS diagnosis and reveal the pathophysiological responses in the brain after ischemic stroke.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article